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Migratory Behavior (migratory + behavior)
Selected AbstractsMigration, Diet, or Molt?BIOTROPICA, Issue 4 2010Interpreting Stable-Hydrogen Isotope Values in Neotropical Bats ABSTRACT Migratory behavior in bats is poorly described, particularly in the Neotropics. Stable-hydrogen isotope (,D) analysis may allow tracking of altitudinal movements of bats but has not been explored. ,D values in rainwater (,Dp) deplete linearly with altitude and are reflected in the keratinous tissues of animals through diet. A mismatch between keratin ,D (,Dk) and that expected at the capture site based on ,Dp can indicate prior migration. We collected rainwater, claws and hair from eight bat species at two lower-montane forest sites in Nicaragua. Claw ,D for Carollia brevicauda and hair and claws for Desmodus rotundus (known to be non-migratory) fell within the predicted range based on rainwater (,17 to ,60,) suggesting these tissues were synthesized at the study site. ,D tissue values for Artibeus toltecus, Sturnira lilium, Glossophaga soricina, Anoura geoffroyi, and hair for C. brevicauda were more negative than predicted for the capture site (,60,) suggesting tissue synthesis at higher elevation and migration downslope to the capture site. However, our study area represents the highest elevation in the region; the nearest appropriate higher elevations are 350,500 km away and seasonal migration is expected to be<200 km. Thus we consider that seasonal shifts in ,Dp (9 to ,45,) may result in differences in species which molt at different times, and that diet may have driven differences in ,D. Our results suggest that the effects of molt timing and diet may first need to be understood before ,D may be successfully used to track bat movements. [source] Drosophila multiplexin (Dmp) modulates motor axon pathfinding accuracyDEVELOPMENT GROWTH & DIFFERENTIATION, Issue 5 2009Frauke Meyer Multiplexins are multidomain collagens typically composed of an N-terminal thrombospondin-related domain, an interrupted triple helix and a C-terminal endostatin domain. They feature a clear regulatory function in the development of different tissues, which is chiefly conveyed by the endostatin domain. This domain can be found in proteolytically released monomeric and trimeric versions, and their diverse and opposed effects on the migratory behavior of epithelial and endothelial cell types have been demonstrated in cell culture experiments. The only Drosophila multiplexin displays specific features of both vertebrate multiplexins, collagens XV and XVIII. We characterized the Drosophila multiplexin (dmp) gene and found that three main isoforms are expressed from it, one of which is the monomeric endostatin version. Generation of dmp deletion alleles revealed that Dmp plays a role in motor axon pathfinding, as the mutants exhibit ventral bypass defects of the intersegmental nerve b (ISNb) similar to other motor axon guidance mutants. Transgenic overexpression of monomeric endostatin as well as of full-length Dmp, but not trimeric endostatin, were able to rescue these defects. In contrast, trimeric endostatin increased axon pathfinding accuracy in wild type background. We conclude that Dmp plays a modulating role in motor axon pathfinding and may be part of a buffering system that functions to avoid innervation errors. [source] Effect of elevated homocysteine on cardiac neural crest migration in vitroDEVELOPMENTAL DYNAMICS, Issue 2 2002Philip R. Brauer Abstract A positive correlation between elevated maternal homocysteine (Hcys) and an increased risk of neural tube, craniofacial, and cardiac defects is well known. Studies suggest Hcys perturbs neural crest (NC) development and may involve N-methyl-D-aspartate (NMDA) receptors (Rosenquist et al., 1999). However, there is no direct evidence that Hcys alters NC cell behavior. Here, we evaluated the effect of Hcys on cardiac NC cell migratory behavior in vitro. Neural tube segments from chick embryos treated in ovo with or without Hcys were placed in culture and the migratory behavior of emigrating NC cells was monitored. Hcys significantly increased in vitro NC cell motility at all embryonic stages examined. NC cell surface area and perimeter were also increased. However, the relative distance NC cells migrated from their original starting point only increased in NC cells treated in ovo at stage 6 or at the time neural tube segments were cultured. Cysteine had no effect. NMDA mimicked Hcys' effect on NC motility and migration distance but had no effect on cell area or perimeter. The noncompetitive inhibitor of NMDA receptors, MK801+, significantly inhibited NC cell motility, reduced migration distance, and also blocked the effects of NMDA and Hcys on NC motility and migratory distance in vitro. A monoclonal antibody directed against the NMDA receptor immunostained NC cells in vitro and, in western blots, bound a single protein with the appropriate molecular weight for the NMDA receptor in NC cell lysates. These data are consistent with the hypothesis that a Hcys-sensitive NMDA-like receptor is expressed by early emigrating NC cells or their precursors, which is important in mediating their migratory behavior. Perturbation of this receptor may be related to some of the teratogenic effects observed with elevated Hcys. © 2002 Wiley-Liss, Inc. [source] Elevation of gene expression for salmon gonadotropin-releasing hormone in discrete brain loci of prespawning chum salmon during upstream migrationDEVELOPMENTAL NEUROBIOLOGY, Issue 2 2005Takeshi Onuma Abstract Our previous studies suggested that salmon gonadotropin-releasing hormone (sGnRH) neurons regulate both final maturation and migratory behavior in homing salmonids. Activation of sGnRH neurons can occur during upstream migration. We therefore examined expression of genes encoding the precursors of sGnRH, sGnRH-I, and sGnRH-II, in discrete forebrain loci of prespawning chum salmon, Oncorhynchus keta. Fish were captured from 1997 through 1999 along their homing pathway: coastal areas, a midway of the river, 4 km downstream of the natal hatchery, and the hatchery. Amounts of sGnRH mRNAs in fresh frozen sections including the olfactory bulb (OB), terminal nerve (TN), ventral telencephalon (VT), nucleus preopticus parvocellularis anterioris (PPa), and nucleus preopticus magnocellularis (PM) were determined by quantitative real-time polymerase chain reactions. The amounts of sGnRH-II mRNA were higher than those of sGnRH-I mRNA, while they showed similar changes during upstream migration. In the OB and TN, the amounts of sGnRH mRNAs elevated from the coast to the natal hatchery. In the VT and PPa, they elevated along with the progress of final maturation. Such elevation was also observed in the rostroventral, middle, and dorsocaudal parts of the PM. The amounts of gonadotropin II, and somatolactin mRNAs in the pituitary also increased consistently with the elevation of gene expression for sGnRH. These results, in combination with lines of previous evidence, indicate that sGnRH neurons are activated in almost all the forebrain loci during the last phases of spawning migration, resulting in coordination of final gonadal maturation and migratory behavior to the spawning ground. © 2005 Wiley Periodicals, Inc. J Neurobiol, 2005 [source] Transplanted glioma cells migrate and proliferate on host brain vasculature: A dynamic analysisGLIA, Issue 8 2006Azadeh Farin Abstract Glioma cells have a remarkable capacity to infiltrate the brain and migrate long distances from the tumor, making complete surgical resection impossible. Yet, little is known about how glioma cells interact with the complex microenvironment of the brain. To investigate the patterns and dynamics of glioma cell infiltration and migration, we stereotactically injected eGFP and DsRed-2 labeled rat C6 glioma cells into neonatal rat forebrains and used time-lapse microscopy to observe glioma cell migration and proliferation in slice cultures generated from these brains. In this model, glioma cells extensively infiltrated the brain by migrating along the abluminal surface of blood vessels. Glioma cells intercalated their processes between the endothelial cells and the perivascular astrocyte end feet, but did not invade into the blood vessel lumen. Dynamic analysis revealed notable similarities between the migratory behavior of glioma cells and that previously observed for glial progenitor cells. Glioma cells had a characteristic leading process and migrated in a saltatory fashion, with bursts of migration separated by periods of immobility, and maximum speeds of over 100 ,m/h. Migrating glioma cells proliferated en route, pausing for as short as an hour to divide before the daughter cells resumed migrating. Remarkably, the majority of glioma cell divisions took place at or near vascular branch points, suggesting that mitosis is triggered by local environmental cues. This study provides the first dynamic analysis of glioma cell infiltration in living brain tissue and reveals that the migration and proliferation of transplanted glioma cells is directed by interactions with host brain vasculature. © 2006 Wiley-Liss, Inc. [source] Embryonic undifferentiated cells show scattering activity on a surface coated with immobilized E-cadherinJOURNAL OF CELLULAR BIOCHEMISTRY, Issue 1 2008Masato Nagaoka Abstract Rearrangement of cell,cell adhesion is a critical event in embryonic development and tissue formation. We investigated the regulatory function of E-cadherin, a key adhesion protein, in the developmental process by using E-cadherin/IgG Fc fusion protein as an adhesion matrix in cell culture. F9 embryonal carcinoma cells usually form colonies when cultured on gelatin or fibronectin matrices. However, F9 cells cultured on the E-cadherin/IgG Fc fusion protein matrix formed a scattered distribution, with a different cytoskeletal organization and E-cadherin-rich protrusions that were regulated by Rac1 activity. The same scattering activity was observed in P19 embryonal carcinoma cells. In contrast, three types of differentiated cells, NMuMG mammary gland cells, MDCK kidney epithelial cells, and mouse primary isolated hepatocytes, did not show the scattering activity observed in F9 and P19 cells. These results suggest that migratory behavior on an E-cadherin-immobilized surface is only observed in embryonic cells, and that the regulatory mechanisms underlying E-cadherin-mediated cell adhesion vary with the state of differentiation. J. Cell. Biochem. 103: 296,310, 2008. © 2007 Wiley-Liss, Inc. [source] 83 Comparative analysis of vertically migrating euglena viridis populations in tidal and non-tidal benthic environmentsJOURNAL OF PHYCOLOGY, Issue 2003M.B. KingstonArticle first published online: 12 JAN 200 Benthic populations of Euglena viridis exhibit vertical migration behavior on high energy intertidal beaches and along the sand banks of freshwater streams. This study examines similarities and differences in the migratory behavior and cell morphology of populations of E. viridis inhabiting Scripps Beach, La Jolla, California and Coble Brook, Burlington, North Carolina. The timing of migration was measured by counting the number of cells in samples collected from the sediment surface throughout the day. Sediment cores were extracted and sectioned to determine the vertical distribution of the population. Neutral density filters and opaque canisters were used to shade the substratum to 56%, 22%, 2%, and 0% of incident irradiance (Io) to examine the effect of light on cell morphology and migratory behavior. On intertidal beaches, E. viridis exhibited a tidal rhythm in vertical migration with cells migrating below the sediment surface at night (>15 cm) and during daytime high tides. In this habitat, the upward migration response was enhanced at irradiances lower than 100% Io but cell morphology was not altered by shading. On the banks of freshwater streams, E. viridis exhibited a diurnal migratory rhythm with both tear-drop and spherical morphologies observed throughout the day. The population was most concentrated at the surface around solar noon and at night it was located between 1 and 2 cm below the surface. Shading did not enhance upward migration but it did affect cell morphology. These results will be interpreted in the context of the dominant selection pressures in each environment. [source] Diel vertical migration of medusae in the open Southern Adriatic Sea over a short time period (July 2003)MARINE ECOLOGY, Issue 1 2009Davor Lu Abstract Diel vertical migration (DVM) of medusae was investigated at a fixed station in the oligotrophic Southern Adriatic Sea at several depths during summer (July) 2003. We hypothesized that medusan DVM is considerably influenced by environmental variables such as hydrographic features, light intensities, and potential prey densities. We used short-term repetitive sampling as an approach to detail these relationships. Of the 26 species collected, the highest abundance was in the layer between the thermocline (15 m) and 100 m depth, where Rhopalonema velatum predominated, reaching the maximum count of 93 individuals per 10 m3. Seven species were observed over a wide depth range: Solmissus albescens (15,1200 m), R. velatum (0,800 m), Persa incolorata (50,1200 m), Octophialucium funerarium (200,1200 m), Arctapodema australis (200,1200 m), Amphinema rubra (100,800 m), and Rhabdoon singulare (15,600). According to the medusan weighted mean depth (WMD) calculations, the longest DVMs were noted for the deep-sea species S. albescens, O. funerarium, and A. australis. The shallowest species, Aglaura hemistoma, was primarily non-migratory. Certain medusan assemblages were associated consistently with a particular depth layer characterized by a particular light intensity. The interplay of environmental factors and trophic relationships explains some of the features of medusan migratory patterns. These findings thus contribute to understanding the variables that determine patterns of medusan vertical migratory behavior. [source] Distinct migratory behavior of early- and late-born neurons derived from the cortical ventricular zoneTHE JOURNAL OF COMPARATIVE NEUROLOGY, Issue 1 2004Yumiko Hatanaka Abstract Time-lapse studies indicate that ventricular zone (VZ)-derived cells show two migratory modes in the cerebral cortex at different stages of mammalian embryogenesis: somal translocation and locomotion. We carried out a systematic analysis to examine whether the migratory behavior of cortical neurons derived from the cortical VZ is stage-dependent. We labeled VZ cells of mouse embryos with green fluorescent protein (gfp) -encoding plasmids by in utero electroporation and evaluated the labeled cells after appropriate survival periods. After electroporation at either embryonic day (E) 12.5 or E15.5, GFP+ VZ cells were initially spindle-shaped and radially oriented. After leaving the VZ, they transformed into round or horizontally oriented fusiform neurons with many short processes. They then seemed to gradually change into radially oriented bipolar cells as they moved upward. Whereas the earliest emigrants from the VZ labeled at E12.5 (early-born neurons) reached the top of the cortical plate (CP) after these changes, VZ cells labeled at E15.5 (late-born neurons) further migrated along the length of radial fibers to reach the top of the CP. A dominant negative form of the gene for cyclin-dependent kinase 5 (Cdk5DN) was then introduced into VZ cells. Transfection of E12.5 VZ with cdk5dn did not disrupt the migration of the early-born neurons. However, this caused a failure in migration of the late-born neurons, although they transformed into bipolar shapes in the intermediate zone. Thus, there appear to be at least two distinct migratory phases of cortical neurons: one common to the early- and late-born neurons, and the other specific to late-born neurons and Cdk5-dependent. J. Comp. Neurol. 479:1,14, 2004. © 2004 Wiley-Liss, Inc. [source] Aberrant seizure-induced neurogenesis in experimental temporal lobe epilepsyANNALS OF NEUROLOGY, Issue 1 2006Jack M. Parent MD Neurogenesis in the hippocampal dentate gyrus persists throughout life and is increased by seizures. The dentate granule cell (DGC) layer is often abnormal in human and experimental temporal lobe epilepsy, with dispersion of the layer and the appearance of ectopic granule neurons in the hilus. We tested the hypothesis that these abnormalities result from aberrant DGC neurogenesis after seizure-induced injury. Bromodeoxyuridine labeling, in situ hybridization, and immunohistochemistry were used to identify proliferating progenitors and mature DGCs in the adult rat pilocarpine temporal lobe epilepsy model. We also examined dentate gyri from epileptic human hippocampal surgical specimens. Prox-1 immunohistochemistry and pulse-chase bromodeoxyuridine labeling showed that progenitors migrate aberrantly to the hilus and molecular layer after prolonged seizures and differentiate into ectopic DGCs in rat. Neuroblast marker expression indicated the delayed appearance of chainlike progenitor cell formations extending into the hilus and molecular layer, suggesting that seizures alter migratory behavior of DGC precursors. Ectopic putative DGCs also were found in the hilus and molecular layer of epileptic human dentate gyrus. These findings indicate that seizure-induced abnormalities of neuroblast migration lead to abnormal integration of newborn DGCs in the epileptic adult hippocampus, and implicate aberrant neurogenesis in the development or progression of recurrent seizures. Ann Neurol 2005 [source] The locust foraging geneARCHIVES OF INSECT BIOCHEMISTRY AND PHYSIOLOGY (ELECTRONIC), Issue 1 2010C. Lucas Abstract Our knowledge of how genes act on the nervous system in response to the environment to generate behavioral plasticity is limited. A number of recent advancements in this area concern food-related behaviors and a specific gene family called foraging (for), which encodes a cGMP-dependent protein kinase (PKG). The desert locust (Schistocerca gregaria) is notorious for its destructive feeding and long-term migratory behavior. Locust phase polyphenism is an extreme example of environmentally induced behavioral plasticity. In response to changes in population density, locusts dramatically alter their behavior, from solitary and relatively sedentary behavior to active aggregation and swarming. Very little is known about the molecular and genetic basis of this striking behavioral phenomenon. Here we initiated studies into the locust for gene by identifying, cloning, and studying expression of the gene in the locust brain. We determined the phylogenetic relationships between the locust PKG and other known PKG proteins in insects. FOR expression was found to be confined to neurons of the anterior midline of the brain, the pars intercerebralis. Our results suggest that differences in PKG enzyme activity are correlated to well-established phase-related behavioral differences. These results lay the groundwork for functional studies of the locust for gene and its possible relations to locust phase polyphenism. © 2010 Wiley Periodicals, Inc. [source] An in vivo comparison of photoactivatable fluorescent proteins in an avian embryo modelDEVELOPMENTAL DYNAMICS, Issue 6 2007Danny A. Stark Abstract Tracing the lineage or neighbor relationships of cells in a migratory population or deep within an embryo is difficult with current methods. The recent explosion of photoactivatable fluorescent proteins (PAFPs) offers a unique cell labeling tool kit, yet their in vivo performance in intact embryos and applicability have not been thoroughly explored. We report a comparison study of PAGFP, PSCFP2, KikGR, and Kaede analyzed in the avian embryo using confocal and 2-photon microscopy. PAFPs were introduced into the chick neural tube by electroporation and each photoconverted in the neural crest or cells in the neural tube with exposure to 405 nm light, but showed dramatic differences in photoefficiency and photostability when compared at the same 2% laser power. KikGR and Kaede photoconverted with ratios only slightly lower than in vitro results, but cells rapidly photobleached after reaching maximal photoefficiency. PSCFP2 had the lowest photoefficiency and photoconverted nearly 70 times slower than the other dual-color PAFPs tested, but was effective at single-cell marking, especially with 2-photon excitation at 760 nm. The dual-color PAFPs were more effective to monitor cell migratory behaviors, since non-photoconverted neighboring cells were fluorescently marked with a separate color. However, photoconverted cells were limited in all cases to be visually distinguishable for long periods, with PSCFP2 visible from background the longest (48 hr). Thus, photoactivation in embryos has the potential to selectively mark less accessible cells with laser accuracy and may provide an effective means to study cell,cell interactions and short-term cell lineage in developmental and stem cell biology. Developmental Dynamics 236:1583,1594, 2007. © 2007 Wiley-Liss, Inc. [source] p120-catenin regulates microtubule dynamics and cell migration in a cadherin-independent mannerGENES TO CELLS, Issue 7 2007Tetsuo Ichii p120-catenin (p120) has been shown to be essential for cadherin stability. Here, we show that p120 is capable of regulating microtubule (MT) dynamics in a cadherin-independent manner. When p120 was depleted in cadherin-deficient Neuro-2a (N2a) cells, MT stability was reduced, as assessed by the nocodazole sensitivity of MTs. On the contrary, over-expression of p120 caused MTs to become resistant to nocodazole. Time-lapse recording of GFP-tagged EB1, a protein which binds the growing plus-ends of MTs, introduced into these cells demonstrated that the plus ends underwent more frequent catastrophe in p120-depleted cells. In addition, p120 knockdown up-regulated the motility of isolated cells, whereas it down-regulated the directional migration of cells from wound edges; and these migratory behaviors of cells were mimicked by nocodazole-induced MT depolymerization. These results suggest that p120 has the ability to regulate MT dynamics and that this activity, in turn, affects cell motility independently of the cadherin adhesion system. [source] | ||||||||||