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    <title>OPUS 4 Latest Documents RSS Feed</title>
    <description>Latest documents</description>
    <link>http://publikationen.stub.uni-frankfurt.de/index/index/</link>
    <pubDate>Fri, 24 May 2013 09:59:40 +0200</pubDate>
    <lastBuildDate>Fri, 24 May 2013 09:59:40 +0200</lastBuildDate>
    <item>
      <title>High functional diversity is related to high nitrogen availability in a deciduous forest - evidence from a functional trait approach</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30005</link>
      <description>The current study tested the assumption that floristic and functional diversity patterns are negatively related to soil nitrogen content. We analyzed 20 plots with soil N-contents ranging from 0.63% to 1.06% in a deciduous forest near Munich (Germany). To describe species adaptation strategies to different nitrogen availabilities, we used a plant functional type (PFT) approach. Each identified PFT represents one realized adaptation strategy to the current environment. These were correlated, next to plant species richness and evenness, to soil nitrogen contents. We found that N-efficient species were typical for low soil nitrogen contents, while N-requiring species occur at high N-contents. In contrast to our initial hypotheses, floristic and functional diversity measures (number of PFTs) were positively related to nitrogen content in the soil. Every functional group has its own adaptation to the prevailing environmental conditions; in consequence, these functional groups can co-exist but do not out-compete one another. The increased number of functional groups at high N-contents leads to increased species richness. Hence, for explaining diversity patterns we need to consider species groups representing different adaptations to the current environmental conditions. Such co-existing ecological strategies may even overcome the importance of competition in their effect on biodiversity.</description>
      <author>Markus Bernhardt-Römermann; Christine Römermann; Valério de Patta Pillar; Thomas Kudernatsch; Anton Fischer</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30005</guid>
      <pubDate>Fri, 24 May 2013 09:59:40 +0200</pubDate>
    </item>
    <item>
      <title>Early otic development depends on autophagy for apoptotic cell clearance and neural differentiation</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30022</link>
      <description>Autophagy is a highly regulated program of self-degradation of the cytosolic constituents that has key roles during early development and in adult cell growth and homeostasis. To investigate the role of autophagy in otic neurogenesis, we studied the expression of autophagy genes in early stages of chicken (Gallus gallus) inner ear development and the consequences of inhibiting the autophagic pathway in organotypic cultures of explanted chicken otic vesicles (OVs). Here we show the expression of autophagy-related genes (Atg) Beclin-1 (Atg6), Atg5 and LC3B (Atg8) in the otocyst and the presence of autophagic vesicles by using transmission electron microscopy in the otic neurogenic zone. The inhibition of the transcription of LC3B by using antisense morpholinos and of class III phosphatidylinositol 3-kinase with 3-methyladenine causes an aberrant morphology of the OV with accumulation of apoptotic cells. Moreover, inhibition of autophagy provokes the misregulation of the cell cycle in the otic epithelium, impaired neurogenesis and poor axonal outgrowth. Finally, our results indicate that autophagy provides the energy required for the clearing of neuroepithelial dying cells and suggest that it is required for the migration of otic neuronal precursors. Taken together, our results show for the first time that autophagy is an active and essential process during early inner ear development.</description>
      <author>Maria Rodriguez Aburto; Hortensia Sánchez-Calderón; Juan M. Hurlé; Isabel Varela-Nieto; Marta Magariños</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30022</guid>
      <pubDate>Thu, 23 May 2013 17:07:25 +0200</pubDate>
    </item>
    <item>
      <title>RAF kinase activity regulates neuroepithelial cell proliferation and neuronal progenitor cell differentiation during early inner ear development</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30018</link>
      <description>Background: Early inner ear development requires the strict regulation of cell proliferation, survival, migration and differentiation, coordinated by the concerted action of extrinsic and intrinsic factors. Deregulation of these processes is associated with embryonic malformations and deafness. We have shown that insulin-like growth factor I (IGF-I) plays a key role in embryonic and postnatal otic development by triggering the activation of intracellular lipid and protein kinases. RAF kinases are serine/threonine kinases that regulate the highly conserved RAS-RAF-MEK-ERK signaling cascade involved in transducing the signals from extracellular growth factors to the nucleus. However, the regulation of RAF kinase activity by growth factors during development is complex and still not fully understood.&#13;
Methodology/Principal Findings: By using a combination of qRT-PCR, Western blotting, immunohistochemistry and in situ hybridization, we show that C-RAF and B-RAF are expressed during the early development of the chicken inner ear in specific spatiotemporal patterns. Moreover, later in development B-RAF expression is associated to hair cells in the sensory patches. Experiments in ex vivo cultures of otic vesicle explants demonstrate that the influence of IGF-I on proliferation but not survival depends on RAF kinase activating the MEK-ERK phosphorylation cascade. With the specific RAF inhibitor Sorafenib, we show that blocking RAF activity in organotypic cultures increases apoptosis and diminishes the rate of cell proliferation in the otic epithelia, as well as severely impairing neurogenesis of the acoustic-vestibular ganglion (AVG) and neuron maturation.&#13;
Conclusions/Significance: We conclude that RAF kinase activity is essential to establish the balance between cell proliferation and death in neuroepithelial otic precursors, and for otic neuron differentiation and axonal growth at the AVG.</description>
      <author>Marta Magariños; Maria Rodriguez Aburto; Hortensia Sánchez-Calderón; Carmen Muñoz-Agudo; Ulf Rüdiger Rapp; Isabel Varela-Nieto</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30018</guid>
      <pubDate>Thu, 23 May 2013 15:08:25 +0200</pubDate>
    </item>
    <item>
      <title>AKT signaling mediates IGF-I survival actions on otic neural progenitors</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30019</link>
      <description>Background: Otic neurons and sensory cells derive from common progenitors whose transition into mature cells requires the coordination of cell survival, proliferation and differentiation programmes. Neurotrophic support and survival of post-mitotic otic neurons have been intensively studied, but the bases underlying the regulation of programmed cell death in immature proliferative otic neuroblasts remains poorly understood. The protein kinase AKT acts as a node, playing a critical role in controlling cell survival and cell cycle progression. AKT is activated by trophic factors, including insulin-like growth factor I (IGF-I), through the generation of the lipidic second messenger phosphatidylinositol 3-phosphate by phosphatidylinositol 3-kinase (PI3K). Here we have investigated the role of IGF-dependent activation of the PI3K-AKT pathway in maintenance of otic neuroblasts.&#13;
Methodology/Principal Findings: By using a combination of organotypic cultures of chicken (Gallus gallus) otic vesicles and acoustic-vestibular ganglia, Western blotting, immunohistochemistry and in situ hybridization, we show that IGF-I-activation of AKT protects neural progenitors from programmed cell death. IGF-I maintains otic neuroblasts in an undifferentiated and proliferative state, which is characterised by the upregulation of the forkhead box M1 (FoxM1) transcription factor. By contrast, our results indicate that post-mitotic p27Kip-positive neurons become IGF-I independent as they extend their neuronal processes. Neurons gradually reduce their expression of the Igf1r, while they increase that of the neurotrophin receptor, TrkC.&#13;
Conclusions/Significance: Proliferative otic neuroblasts are dependent on the activation of the PI3K-AKT pathway by IGF-I for survival during the otic neuronal progenitor phase of early inner ear development.</description>
      <author>Maria Rodriguez Aburto; Marta Magariños; Yolanda Leon; Isabel Varela-Nieto; Hortensia Sanchez-Calderon</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30019</guid>
      <pubDate>Thu, 23 May 2013 14:55:27 +0200</pubDate>
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      <title>Autophagy during vertebrate development</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30013</link>
      <description>Autophagy is an evolutionarily conserved catabolic process by which cells degrade their own components through the lysosomal machinery. In physiological conditions, the mechanism is tightly regulated and contributes to maintain a balance between synthesis and degradation in cells undergoing intense metabolic activities. Autophagy is associated with major tissue remodeling processes occurring through the embryonic, fetal and early postnatal periods of vertebrates. Here we survey current information implicating autophagy in cellular death, proliferation or differentiation in developing vertebrates. In developing systems, activation of the autophagic machinery could promote different outcomes depending on the cellular context. Autophagy is thus an extraordinary tool for the developing organs and tissues.</description>
      <author>Maria Rodriguez Aburto; Juan M. Hurlé; Isabel Varela-Nieto; Marta Magariños</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30013</guid>
      <pubDate>Thu, 23 May 2013 13:03:42 +0200</pubDate>
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      <title>Do non-genomically encoded fusion transcripts cause recurrent chromosomal translocations?</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30011</link>
      <description>We among others have recently demonstrated that normal cells produce “fusion mRNAs”. These fusion mRNAs do not derive from rearranged genomic loci, but rather they are derived from “early-terminated transcripts” (ETTs). Premature transcriptional termination takes place in intronic sequences that belong to “breakpoint cluster regions”. One important property of ETTs is that they exhibit an unsaturated splice donor site. This results in: (1) splicing to “cryptic exons” present in the final intron; (2) Splicing to another transcript of the same gene (intragenic trans-splicing), resulting in “exon repetitions”; (3) splicing to a transcript of another gene (intergenic trans-splicing), leading to “non-genomically encoded fusion transcripts” (NGEFTs). These NGEFTs bear the potential risk to influence DNA repair processes, since they share identical nucleotides with their DNA of origin, and thus, could be used as “guidance RNA” for DNA repair processes. Here, we present experimental data about four other genes. Three of them are associated with hemato-malignancies (ETV6, NUP98 and RUNX1), while one is associated with solid tumors (EWSR1). Our results demonstrate that all genes investigated so far (MLL, AF4, AF9, ENL, ELL, ETV6, NUP98, RUNX1 and EWSR1) display ETTs and produce transpliced mRNA species, indicating that this is a genuine property of translocating genes.</description>
      <author>Eric Kowarz; Theodor Dingermann; Rolf Marschalek</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30011</guid>
      <pubDate>Thu, 23 May 2013 12:21:54 +0200</pubDate>
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      <title>Venomous Secretions from Marine Snails of the Terebridae Family Target Acetylcholine Receptors</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/26346</link>
      <description>Venoms from cone snails (Conidae) have been extensively studied during the last decades, but those from other members of the suborder Toxoglossa, such as of Terebridae and Turridae superfamilies attracted less interest so far. Here, we report the effects of venom and gland extracts from three species of the superfamily Terebridae. By 2-electrode voltage-clamp technique the gland extracts were tested on Xenopus oocytes expressing nicotinic acetylcholine receptors (nAChRs) of rat neuronal (α3β2, α3β4, α4β2, α4β4, α7) and muscle subtypes (α1β1γδ), and expressing potassium (Kv1.2 and Kv1.3) and sodium channels (Nav1.2, 1.3, 1.4, 1.6). The extracts were shown to exhibit remarkably high inhibitory activities on almost all nAChRs tested, in particular on the α7 subtype suggesting the presence of peptides of the A-superfamily from the venom of Conus species. In contrast, no effects on the potassium and sodium channels tested were observed. The venoms of terebrid snails may offer an additional source of novel biologically active peptides.</description>
      <author>Yvonne Kendel; Christian Melaun; Alexander Kurz; Annette Nicke; Steve Peigneur; Jan Tytgat; Cora Wunder; Dietrich Mebs; Silke Kauferstein</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/26346</guid>
      <pubDate>Thu, 23 May 2013 11:19:28 +0200</pubDate>
    </item>
    <item>
      <title>Biological activities of ethanolic extracts from deep-sea antarctic marine sponges</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/26347</link>
      <description>We report on the screening of ethanolic extracts from 33 deep-sea Antarctic marine sponges for different biological activities. We monitored hemolysis, inhibition of acetylcholinesterase, cytotoxicity towards normal and transformed cells and growth inhibition of laboratory, commensal and clinically and ecologically relevant bacteria. The most prominent activities were associated with the extracts from sponges belonging to the genus Latrunculia, which show all of these activities. While most of these activities are associated to already known secondary metabolites, the extremely strong acetylcholinesterase inhibitory potential appears to be related to a compound unknown to date. Extracts from Tetilla leptoderma, Bathydorus cf. spinosus, Xestospongia sp., Rossella sp., Rossella cf. racovitzae and Halichondria osculum were hemolytic, with the last two also showing moderate cytotoxic potential. The antibacterial tests showed significantly greater activities of the extracts of these Antarctic sponges towards ecologically relevant bacteria from sea water and from Arctic ice. This indicates their ecological relevance for inhibition of bacterial microfouling.</description>
      <author>Tom Turk; Jerneja Ambrožič Avguštin; Urška Batista; Gašper Strugar; Rok Kosmina; Sandra Čivović; Dorte Janussen; Silke Kauferstein; Dietrich Mebs; Kristina Sepčić</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/26347</guid>
      <pubDate>Thu, 23 May 2013 11:05:02 +0200</pubDate>
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      <title>Unmanned Aerial Vehicle (UAV) for Monitoring Soil Erosion in Morocco</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/26348</link>
      <description>This article presents an environmental remote sensing application using a UAV that is specifically aimed at reducing the data gap between field scale and satellite scale in soil erosion monitoring in Morocco. A fixed-wing aircraft type Sirius I (MAVinci, Germany) equipped with a digital system camera (Panasonic) is employed. UAV surveys are conducted over different study sites with varying extents and flying heights in order to provide both very high resolution site-specific data and lower-resolution overviews, thus fully exploiting the large potential of the chosen UAV for multi-scale mapping purposes. Depending on the scale and area coverage, two different approaches for georeferencing are used, based on high-precision GCPs or the UAV’s log file with exterior orientation values respectively. The photogrammetric image processing enables the creation of Digital Terrain Models (DTMs) and ortho-image mosaics with very high resolution on a sub-decimetre level. The created data products were used for quantifying gully and badland erosion in 2D and 3D as well as for the analysis of the surrounding areas and landscape development for larger extents.</description>
      <author>Sebastian D'Oleire-Oltmanns; Irene Marzolff; Klaus Daniel Peter; Johannes B. Ries</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/26348</guid>
      <pubDate>Thu, 23 May 2013 10:45:29 +0200</pubDate>
    </item>
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      <title>Molecular Mechanisms of Adaptation of the Moderately Halophilic Bacterium Halobacillis halophilus to Its Environment</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30010</link>
      <description>The capability of osmoadaptation is a prerequisite of organisms that live in an environment with changing salinities. Halobacillus halophilus is a moderately halophilic bacterium that grows between 0.4 and 3 M NaCl by accumulating both chloride and compatible solutes as osmolytes. Chloride is absolutely essential for growth and, moreover, was shown to modulate gene expression and activity of enzymes involved in osmoadaptation. The synthesis of different compatible solutes is strictly salinity- and growth phase-dependent. This unique hybrid strategy of H. halophilus will be reviewed here taking into account the recently published genome sequence. Based on identified genes we will speculate about possible scenarios of the synthesis of compatible solutes and the uptake of potassium ion which would complete our knowledge of the fine-tuned osmoregulation and intracellular osmolyte balance in H. halophilus.</description>
      <author>Inga Hänelt; Volker Müller</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30010</guid>
      <pubDate>Thu, 23 May 2013 10:28:33 +0200</pubDate>
    </item>
    <item>
      <title>Predator avoidance in extremophile fish</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30007</link>
      <description>Extreme habitats are often characterized by reduced predation pressures, thus representing refuges for the inhabiting species. The present study was designed to investigate predator avoidance of extremophile populations of Poecilia mexicana and P. sulphuraria that either live in hydrogen sulfide-rich (sulfidic) springs or cave habitats, both of which are known to have impoverished piscine predator regimes. Focal fishes that inhabited sulfidic springs showed slightly weaker avoidance reactions when presented with several naturally occurring predatory cichlids, but strongest differences to populations from non-sulfidic habitats were found in a decreased shoaling tendency with non-predatory swordtail (Xiphophorus hellerii) females. When comparing avoidance reactions between P. mexicana from a sulfidic cave (Cueva del Azufre) and the adjacent sulfidic surface creek (El Azufre), we found only slight differences in predator avoidance, but surface fish reacted much more strongly to the non-predatory cichlid Vieja bifasciata. Our third experiment was designed to disentangle learned from innate effects of predator recognition. We compared laboratory-reared (i.e., predator-naïve) and wild-caught (i.e., predator-experienced) individuals of P. mexicana from a non-sulfidic river and found no differences in their reaction towards the presented predators. Overall, our results indicate (1) that predator avoidance is still functional in extremophile Poecilia spp. and (2) that predator recognition and avoidance reactions have a strong genetic basis.</description>
      <author>David Bierbach; Matthias Schulte; Nina Herrmann; Claudia Zimmer; Lenin Arias-Rodriguez; Jeane Rimber Indy; Rüdiger Riesch; Martin Plath</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30007</guid>
      <pubDate>Thu, 23 May 2013 10:05:45 +0200</pubDate>
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      <title>Impact of climate change on renewable groundwater resources: assessing the benefits of avoided greenhouse gas emissions using selected CMIP5 climate projections</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30001</link>
      <description>Reduction of greenhouse gas (GHG) emissions to minimize climate change requires very significant societal effort. To motivate this effort, it is important to clarify the benefits of avoided emissions. To this end, we analysed the impact of four emissions scenarios on future renewable groundwater resources, which range from 1600 GtCO2 during the 21st century (RCP2.6) to 7300 GtCO2 (RCP8.5). Climate modelling uncertainty was taken into account by applying the bias-corrected output of a small ensemble of five CMIP5 global climate models (GCM) as provided by the ISI-MIP effort to the global hydrological model WaterGAP. Despite significant climate model uncertainty, the benefits of avoided emissions with respect to renewable groundwater resources (i.e. groundwater recharge (GWR)) are obvious. The percentage of projected global population (SSP2 population scenario) suffering from a significant decrease of GWR of more than 10% by the 2080s as compared to 1971–2000 decreases from 38% (GCM range 27–50%) for RCP8.5 to 24% (11–39%) for RCP2.6. The population fraction that is spared from any significant GWR change would increase from 29% to 47% if emissions were restricted to RCP2.6. Increases of GWR are more likely to occur in areas with below average population density, while GWR decreases of more than 30% affect especially (semi)arid regions, across all GCMs. Considering change of renewable groundwater resources as a function of mean global temperature (GMT) rise, the land area that is affected by GWR decreases of more than 30% and 70% increases linearly with global warming from 0 to 3 ° C. For each degree of GMT rise, an additional 4% of the global land area (except Greenland and Antarctica) is affected by a GWR decrease of more than 30%, and an additional 1% is affected by a decrease of more than 70%.</description>
      <author>Felix Theodor Portmann; Petra Döll; Stephanie Eisner; Martina Flörke</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30001</guid>
      <pubDate>Thu, 23 May 2013 09:52:28 +0200</pubDate>
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      <title>Implementing transparency in an Eastern European office market: preparing Warsaw for global investments</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30000</link>
      <description>In the aftermath of an increasing integration of property and financial markets, the real estate industry is subject to soaring internationalization processes. Since international institutional investors appeared, transnational real estate investments have increased tremendously. In recent years, Central and Eastern European countries have been becoming more attractive to institutional investors and are therefore being integrated into international market structures. Within these countries, Warsaw emerged as the most dynamic and important real estate market. But what are the mechanisms and practices through which the real estate market of Warsaw becomes international? Which networks, intermediaries and frames are necessary to constitute a mature real estate market? The article argues that international real estate consultants are playing a crucial role in the underlying internationalization process. They are acting at the interface between investors, developers, construction companies and tenants and are therefore becoming a crucial hinge between real estate actors. With the example of the Warsaw real estate market we argue that international real estate consultancies are key drivers of the transformation process from a local to a global market. They transfer global knowledge, competence and practices and implement transparent and professional structures in the emerging Warsaw real estate market.</description>
      <author>Nadine Bitterer; Susanne Heeg</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/30000</guid>
      <pubDate>Wed, 22 May 2013 15:57:03 +0200</pubDate>
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      <title>CD69 Is a TGF-β/1α,25-dihydroxyvitamin D3 Target Gene in Monocytes </title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29924</link>
      <description>CD69 is a transmembrane lectin that can be expressed on most hematopoietic cells. In monocytes, it has been functionally linked to the 5-lipoxygenase pathway in which the leukotrienes, a class of highly potent inflammatory mediators, are produced. However, regarding CD69 gene expression and its regulatory mechanisms in monocytes, only scarce data are available. Here, we report that CD69 mRNA expression, analogous to that of 5-lipoxygenase, is induced by the physiologic stimuli transforming growth factor-β (TGF-β) and 1α,25-dihydroxyvitamin D3 (1α,25(OH)2D3) in monocytic cells. Comparison with T- and B-cell lines showed that the effect was specific for monocytes. CD69 expression levels were increased in a concentration-dependent manner, and kinetic analysis revealed a rapid onset of mRNA expression, indicating that CD69 is a primary TGF-β/1α,25(OH)2D3 target gene. PCR analysis of different regions of the CD69 mRNA revealed that de novo transcription was initiated and proximal and distal parts were induced concomitantly. In common with 5-lipoxygenase, no activation of 0.7 kb or ~2.3 kb promoter fragments by TGF-β and 1α,25(OH)2D3 could be observed in transient reporter assays for CD69. Analysis of mRNA stability using a transcription inhibitor and a 3′UTR reporter construct showed that TGF-β and 1α,25(OH)2D3 do not influence CD69 mRNA stability. Functional knockdown of Smad3 clearly demonstrated that upregulation of CD69 mRNA, in contrast to 5-LO, depends on Smad3. Comparative studies with different inhibitors for mitogen activated protein kinases (MAPKs) revealed that MAPK signalling is involved in CD69 gene regulation, whereas 5-lipoxygenase gene expression was only partly affected. Mechanistically, we found evidence that CD69 gene upregulation depends on TAK1-mediated p38 activation. In summary, our data indicate that CD69 gene expression, conforming with 5-lipoxygenase, is regulated monocyte-specifically by the physiologic stimuli TGF-β and 1α,25(OH)2D3 on mRNA level, although different mechanisms account for the upregulation of each gene.</description>
      <author>Thea K. Wöbke; Andreas von Knethen; Dieter Steinhilber; Bernd L. Sorg</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29924</guid>
      <pubDate>Fri, 17 May 2013 13:28:34 +0200</pubDate>
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    <item>
      <title>Restriction of trophic factors and nutrients induces PARKIN expression</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29905</link>
      <description>Parkinson's disease (PD) is the most frequent neurodegenerative movement disorder and manifests at old age. While many details of its pathogenesis remain to be elucidated, in particular the protein and mitochondrial quality control during stress responses have been implicated in monogenic PD variants. Especially the mitochondrial kinase PINK1 and the ubiquitin ligase PARKIN are known to cooperate in autophagy after mitochondrial damage. As autophagy is also induced by loss of trophic signaling and PINK1 gene expression is modulated after deprivation of cytokines, we analyzed to what extent trophic signals and starvation stress regulate PINK1 and PARKIN expression. Time course experiments with serum deprivation and nutrient starvation of human SH-SY5Y neuroblastoma cells and primary mouse neurons demonstrated phasic induction of PINK1 transcript up to twofold and PARKIN transcript levels up to sixfold. The corresponding threefold starvation induction of PARKIN protein was limited by its translocation to lysosomes. Analysis of primary mouse cells from PINK1-knockout mice indicated that PARKIN induction and lysosomal translocation occurred independent of PINK1. Suppression of the PI3K-Akt-mTOR signaling by pharmacological agents modulated PARKIN expression accordingly. In conclusion, this expression survey demonstrates that PARKIN and PINK1 are coregulated during starvation and suggest a role of both PD genes in response to trophic signals and starvation stress.</description>
      <author>Michael Klinkenberg; Suzana Gispert; Jorge Antolio Dominguez Bautista; Isabelle Braun; Georg Auburger; Marina Jendrach</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29905</guid>
      <pubDate>Mon, 13 May 2013 16:23:10 +0200</pubDate>
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    <item>
      <title>Survival analysis of HDR brachytherapy versus reoperation versus temozolomide alone: a retrospective cohort analysis of recurrent glioblastoma multiforme</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29491</link>
      <description>Objectives Tumour recurrence of glioblastoma multiforme (GBM) after initial treatment with surgical resection, radiotherapy and chemotherapy is an inevitable phenomenon. This retrospective cohort study compared the efficacy of interstitial high dose rate brachytherapy (HDR-BRT), re-resection and sole dose dense temozolomide chemotherapy (ddTMZ) in the treatment of recurrent glioblastoma after initial surgery and radiochemotherapy.&#13;
Design Retropective cohort study.&#13;
Setting Primary level of care with two participating centres. The geographical location was central Germany.&#13;
Participants From January 2005 to December 2010, a total of 111 patients developed recurrent GBM after initial surgery and radiotherapy with concomitant temozolomide. The inclusion criteria were as follows: (1) histology-proven diagnosis of primary GBM (WHO grade 4), (2) primary treatment with resection and radiochemotherapy, and (3) tumour recurrence/progression.&#13;
Interventions This study compared retrospectively the efficacy of interstitial HDR-BRT, re-resection and ddTMZ alone in the treatment of recurrent glioblastoma.&#13;
Primary and secondary outcome measures Median survival, progression free survival and complication rate.&#13;
Results Median survival after salvage therapy of the recurrence was 37, 30 and 26 weeks, respectively. The HDR-BRT group did significantly better than both the reoperation (p&lt;0.05) and the ddTMZ groups (p&lt;0.05). Moderate to severe complications in the HDR-BRT, reoperation and sole chemotherapy groups occurred in 5/50 (10%), 4/36 (11%) and 9/25 (36%) cases, respectively.&#13;
Conclusions CT-guided interstitial HDR-BRT attained higher survival benefits in the management of recurrent glioblastoma after initial surgery and radiotherapy with concurrent temozolomide in comparison with the other treatment modalities. The low risk of complications of the HDR-BRT and the fact that it can be delivered percutaneously in local anaesthesia render it a promissing treatment option for selected patients which should be further evaluated.</description>
      <author>Eleftherios Archavlis; Nikolaos Tselis; Gerhard Birn; Peter Ulrich; Dimos Baltas; Nikolaos Zamboglou</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29491</guid>
      <pubDate>Mon, 13 May 2013 16:04:47 +0200</pubDate>
    </item>
    <item>
      <title>Platypnea-orthodeoxia due to osteoporosis and severe kyphosis: a rare cause for dyspnea and hypoxemia</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29494</link>
      <description>Platypnea orthodeoxia is a rare disorder characterized by dyspnea and arterial desaturation, exacerbated by the upright position and relieved when the subject is recumbent. We report the case of a 79-year old woman admitted to hospital with dyspnea who was thought to have restrictive ventilatory impairment due to osteoporosis and severe kyphosis. Interestingly, the dyspnea was aggravated in the upright position, whereas the symptoms improved in the supine position. Arterial blood gas analysis confirmed orthodeoxia. The lung function test showed only a mild obstructive and restrictive ventilation disorder. Echocardiography revealed a patent foramen ovale and an aneurysm of the atrial septum protruding into the left atrium, despite normal right atrial pressure. Transesophageal echocardiography showed a prominent Eustachian valve guiding a blood flow from the inferior vena cava directly onto the atrial septum, thereby pushing open the patent foramen ovale. Contrast-enhanced echocardiography confirmed a spontaneous right-to-left shunt through the patent foramen ovale. It was assumed that the platypnea-orthodeoxia was caused by a prominent Eustachian valve redirected to the patent foramen ovale as a result of severe osteoporosis with subsequent thoracic kyphosis and a change in the position of the entire heart. The patient underwent permanent transcatheter closure of the patent foramen ovale after hemodynamic assessment had confirmed a significant right-to-left shunt through it. After the procedure the arterial oxygen pressure increased significantly in the upright position and dyspnea improved.</description>
      <author>Claudius Teupe; Gerian Groenefeld</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29494</guid>
      <pubDate>Mon, 13 May 2013 15:16:25 +0200</pubDate>
    </item>
    <item>
      <title>The magnetite-based receptors in the beak of birds and their role in avian navigation</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29867</link>
      <description>Iron-rich structures have been described in the beak of homing pigeons, chickens and several species of migratory birds and interpreted as magnetoreceptors. Here, we will briefly review findings associated with these receptors that throw light on their nature, their function and their role in avian navigation. Electrophysiological recordings from the ophthalmic nerve, behavioral studies and a ZENK-study indicate that the trigeminal system, the nerves innervating the beak, mediate information on magnetic changes, with the electrophysiological study suggesting that these are changes in intensity. Behavioral studies support the involvement of magnetite and the trigeminal system in magnetoreception, but clearly show that the inclination compass normally used by birds represents a separate system. However, if this compass is disrupted by certain light conditions, migrating birds show 'fixed direction' responses to the magnetic field, which originate in the receptors in the beak. Together, these findings point out that there are magnetite-based magnetoreceptors located in the upper beak close to the skin. Their natural function appears to be recording magnetic intensity and thus providing one component of the multi-factorial 'navigational map' of birds.</description>
      <author>Roswitha Wiltschko; Wolfgang Wiltschko</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29867</guid>
      <pubDate>Fri, 10 May 2013 13:06:48 +0200</pubDate>
    </item>
    <item>
      <title>Correlation from undiluted vitreous cytokines of untreated central retinal vein occlusion with spectral domain optical coherence tomography</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29865</link>
      <description>Purpose: To correlate inflammatory and proangiogenic key cytokines from undiluted vitreous of treatment-naïve central retinal vein occlusion (CRVO) patients with SD-OCT parameters.&#13;
Methods: Thirty-five patients (age 71.1 years, 24 phakic, 30 nonischemic) underwent intravitreal combination therapy, including a single-site 23-gauge core vitrectomy. Twenty-eight samples from patients with idiopathic, non-uveitis floaterectomy served as controls. Interleukin 6 (IL-6), monocyte chemoattractant protein-1 (MCP-1), and vascular endothelial growth factor (VEGF-A) levels were correlated with the visual acuity (logMar), category of CRVO (ischemic or nonischemic) and morphologic parameters, such as central macular thickness-CMT, thickness of neurosensory retina-TNeuro, extent of serous retinal detachment-SRT and disintegrity of the IS/OS and others.&#13;
Results: The mean IL-6 was 64.7pg/ml (SD ± 115.8), MCP-1 1015.7 ( ± 970.1), and VEGF-A 278.4 ( ± 512.8), which was significantly higher than the control IL-6 6.2 ± 3.4pg/ml (P=0.06), MCP-1 253.2 ± 73.5 (P&lt;0.0000001) and VEGF-A 7.0 ± 4.9 (P&lt;0.0006). All cytokines correlated highly with one another (correlation coefficient r=0.82 for IL-6 and MCP-1; r=0.68 for Il-6 and VEGF-A; r=0.64 for MCP-1 and VEGF-A). IL-6 correlated significantly with CMT, TRT, SRT, dIS/OS, and dELM. MCP-1 correlated significantly with SRT, dIS/OS, and dELM. VEGF-A correlated not with changes in SD-OCT, while it had a trend to be higher in the ischemic versus the nonischemic CRVO group (P=0.09).&#13;
Conclusions: The inflammatory cytokines were more often correlated with morphologic changes assessed by SD-OCT, whereas VEGF-A did not correlate with CRVO-associated changes in SD-OCT. VEGF inhibition alone may not be sufficient in decreasing the inflammatory response in CRVO therapy.</description>
      <author>Michael Janusz Koss; Marcel Pfister; Florian Rothweiler; R Rejdak; R Ribeiro; Jindrich Cinatl; R Schubert; Thomas Kohnen; Frank H. Koch</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29865</guid>
      <pubDate>Fri, 10 May 2013 12:35:28 +0200</pubDate>
    </item>
    <item>
      <title>Effect of sonic hedgehog/β-TCP composites on bone healing within the critical-sized rat femoral defect</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29866</link>
      <description>The creation of entirely synthetically derived bone substitute materials which are as effective as autologous bone grafts is desirable. Osteogenesis involves the concerted action of several proteins within a signaling cascade. Hedgehog proteins act upstream of this cascade, inducing the expression of various bone morphogenetic proteins (BMPs) and promoting physiological bone healing. Therefore, the hypothesis that hedgehog signaling in bone defects improves bone healing more than BMP signaling alone was tested. Recombinant N-terminal sonic hedgehog protein (N-SHh), BMP-2 or a combination of the two was added to β-tricalcium phosphate (β-TCP) and 5-mm femoral midshaft defects in nude rats were filled with these composites. The defects were stabilized with mini-plates. After eight weeks, the animals were sacrificed and the femora were explanted. The radiological evaluation was followed by a three-point bending test and histological examination. BMP-2/β-TCP composites showed a trend of increased stiffness compared with the controls (β-TCP without protein). N-SHh/β-TCP composites had lower stiffness compared with the control group and the N-SHh/BMP-2/β-TCP composites also had lower average stiffness compared with the controls (all not significant). Histomorphometry, however, revealed abundant cartilage and bone core formation in the N-SHh-composite groups. The sum of the new cartilage and bone was highest in the combination group N-SHh/BMP-2 (not significant). The addition of N-SHh to bone substitute materials appears to delay bone healing at the applied concentration and observation time but also showed a trend for higher amounts of ossifying cartilage.</description>
      <author>Jörg Warzecha; Caroline Seebach; Armin Flinspach; Florian Wenger; Dirk Henrich; Ingo Marzi</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29866</guid>
      <pubDate>Fri, 10 May 2013 12:29:27 +0200</pubDate>
    </item>
    <item>
      <title>The role of recombinant epidermal growth factor and serotonin in the stimulation of tumor growth in a SCCHN xenograft model</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29868</link>
      <description>One challenge of squamous cell carcinoma of the head and neck (SCCHN) chemotherapy is a small percentage of tumor cells that arrest in the G0 phase of the cell cycle and are thus not affected by chemotherapy. This could be one reason for tumor recurrence at a later date. The recruitment of these G0-arresting cells into the active cell cycle and thus, proliferation, may increase the efficacy of chemotherapeutic agents. The aim of this study was to investigate whether stimulation with recombinant epidermal growth factor (EGF) or serotonin leads to an increased tumor cell proliferation in xenografts. Detroit 562 cells were injected into NMRI-Foxn1nu mice. Treatment was performed with 15 µg murine or human EGF, or 200 µg serotonin. The control mice were treated with Lactated Ringer's solution (5 mice/group). Tumor size was measured on days 4, 8 and 12 after tumor cell injection. The EGF stimulated mice showed a significantly higher tumor growth compared to the serotonin-stimulated mice and the untreated controls. In the present study, we show that it is possible to stimulate tumor cells in xenografts by EGF and thus, enhance cell proliferation, resulting in a higher tumor growth compared to the untreated control group. In our future investigations, we plan to include a higher number of mice, an adjustment of the EGF dosage and cell subanalysis, considering the heterogeneity of SCCHN tumors.</description>
      <author>Christin Geissler; Markus Hambek; Anne Eckardt; Christoph Arnoldner; Marc Diensthuber; Timo Stöver; Jens Wagenblast</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29868</guid>
      <pubDate>Fri, 10 May 2013 10:12:04 +0200</pubDate>
    </item>
    <item>
      <title>Thrombolysis in a stroke patient on dabigatran anticoagulation: case report and synopsis of published cases</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29876</link>
      <description>We present the case of an aphasic 77-year-old stroke patient with left distal M1 occlusion who received rt-PA for thrombolysis while on oral anticoagulant treatment with dabigatran (150 mg b.i.d.). Coagulation parameters were normal (thrombin time 20 s, aPTT 20 s, INR 1.08) and the patient improved from an NIHSS of 15 to 5 within 24 h with sonographic evidence of M1 recanalization. She did not develop intracranial bleeding complications but showed unusually large diffuse skin ecchymoses. In our report, we give an overview of all reported cases of thrombolysis under dabigatran anticoagulation and discuss the questions of medication adherence under novel oral anticoagulants (NOA) and the safety of NOA in terms of secondary intracerebral hemorrhage after stroke.</description>
      <author>Waltraud Pfeilschifter; Mario Abruscato; Susanne Hövelmann; Horst Baas</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29876</guid>
      <pubDate>Fri, 10 May 2013 09:52:11 +0200</pubDate>
    </item>
    <item>
      <title>First human study in treatment of unresectable liver metastases from colorectal cancer with irinotecan-loaded beads (DEBIRI)</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29899</link>
      <description>The objective of this pilot clinical study was to assess the safety, technical feasibility, pharmacokinetic (PK) profile and tumour response of DC Bead™ with irinotecan (DEBIRI™) delivered by intra-arterial embolisation for the treatment of metastatic colorectal cancer. Eleven patients with unresectable liver metastases from CRC, tumour burden &lt;30% of liver volume, adequate haematological, liver and renal function, performance status of &lt;2 were included in this study. Patients received up to 4 sessions of TACE with DEBIRI at 3-week intervals. Feasibility of the procedure, safety and tumour response were assessed after each cycle. PK was measured after the first cycle. Patients were followed up to 24 weeks. Only mild to moderate adverse events were observed. DEBIRI is a technically feasibile procedure; no technical complications were observed. Average Cmax for irinotecan and SN-38 was 194 ng/ml and 16.7 ng/ml, respectively, with average t½ of 4.6 h and 12.4 h following administration of DEBIRI. Best overall response during the study showed disease control in 9 patients (2 patients with partial response and 7 with stable disease, overall response rate of 18%). Our study shows that transarterial chemoembolisation with irinotecan-loaded DC beads (DEBIRI) is safe, technically feasible and effective with a good PK profile.</description>
      <author>Katrin Eichler; Stephan Zangos; Martin G. Mack; Renate Maria Hammerstingl; Tatjana Gruber-Rouh; Christof Gallus; Thomas J. Vogl</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29899</guid>
      <pubDate>Wed, 08 May 2013 16:40:29 +0200</pubDate>
    </item>
    <item>
      <title>Transfer entropy - a model-free measure of effective connectivity for the neurosciences</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29499</link>
      <description>Understanding causal relationships, or effective connectivity, between parts of the brain is of utmost importance because a large part of the brain’s activity is thought to be internally generated and, hence, quantifying stimulus response relationships alone does not fully describe brain dynamics. Past efforts to determine effective connectivity mostly relied on model based approaches such as Granger causality or dynamic causal modeling. Transfer entropy (TE) is an alternative measure of effective connectivity based on information theory. TE does not require a model of the interaction and is inherently non-linear. We investigated the applicability of TE as a metric in a test for effective connectivity to electrophysiological data based on simulations and magnetoencephalography (MEG) recordings in a simple motor task. In particular, we demonstrate that TE improved the detectability of effective connectivity for non-linear interactions, and for sensor level MEG signals where linear methods are hampered by signal-cross-talk due to volume conduction.</description>
      <author>Raul Vicente; Michael Wibral; Michael Lindner; Gordon Pipa</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29499</guid>
      <pubDate>Wed, 08 May 2013 13:19:17 +0200</pubDate>
    </item>
    <item>
      <title>Static stretching of the hamstrings muscle for injury prevention in football codes: a systematic review</title>
      <link>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29863</link>
      <description>Purpose: Hamstring injuries are common among football players. There is still disagreement regarding prevention. The aim of this review is to determine whether static stretching reduces hamstring injuries in football codes.&#13;
Methods: A systematic literature search was conducted on the online databases PubMed, PEDro, Cochrane, Web of Science, Bisp and Clinical Trial register. Study results were presented descriptively and the quality of the studies assessed were based on Cochrane’s ‘risk of bias’ tool.&#13;
Results: The review identified 35 studies, including four analysis studies. These studies show deficiencies in the quality of study designs.&#13;
Conclusion: The study protocols are varied in terms of the length of intervention and follow-up. No RCT studies are available, however, RCT studies should be conducted in the near future.&#13;
</description>
      <author>Slavko Rogan; Dirk Wüst; Thomas Schwitter; Dietmar Schmidtbleicher</author>
      <category>article</category>
      <guid>http://publikationen.stub.uni-frankfurt.de/frontdoor/index/index/docId/29863</guid>
      <pubDate>Wed, 08 May 2013 12:49:31 +0200</pubDate>
    </item>
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