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10.1369/0022155415575027 http://scihub22266oqcxt.onion/10.1369/0022155415575027 C4409944!4409944!25673286     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Histochem+Cytochem 2015 ; 63 (5): 367-83 Nephropedia Template TP {{tp|p=25673286|t=2015. Glial and Perivascular Structures in the Subfornical Organ: Distinguishing the Shell and Core |pdf=|usr=}}{{25673286}} gab.com Text Glial and Perivascular Structures in the Subfornical Organ: Distinguishing the Shell and Core JO: J Histochem Cytochem http://www.kidney.de/pget.php?&tw=1&pmid=25673286 #FOAvip The subfornical organ (SFO) is a circumventricular organ with a chemosensitive function, and its vessels have no blood-brain barrier. Our study investigated the glial and vascular components in the SFO to determine whether their distributions indicate subdivisions, how to characterize the vessels and how to demarcate the SFO. To this end, we investigated glial markers (GFAP, glutamine synthetase, S100) and other markers, including vimentin and nestin (immature glia), laminin (basal lamina), ?-dystroglycan (glio-vascular connections), and aquaporin 4 (glial water channels). We determined that the ?shell? of the SFO was marked by immunoreactivity for S100, GFAP and aquaporin 4. Nestin immunoreactivity was characteristic of the ?core?. Vimentin was almost evenly distributed. Glutamine synthetase immunoreactivity occurred in the shell but its expression was sparse. Vessels in the core were decorated with laminin but showed a discontinuous expression of aquaporin 4. Vimentin and GFAP staining was usually in separate glial elements, which may be related to their functional differences. Similar to other vessels in the brain, ?-dystroglycan was detected along the shell vessels but laminin was not. The gradual disappearance of the laminin immunopositivity was attributed to the gradual disappearance of the perivascular space. Thus, our findings suggest that the shell and core glio-vascular structures are adapted to different sensory functions: osmoperception and the perception of circulating peptides, respectively. Twit Text FOAVip Glial and Perivascular Structures in the Subfornical Organ: Distinguishing the Shell and Core ????J Histochem Cytochem http://www.kidney.de/pget.php?&tw=1&pmid=25673286 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25673286 #FOAvip English Wikipedia <ref>{{Cite pmid|25673286}}</ref> Glial and Perivascular Structures in the Subfornical Organ: Distinguishing the Shell and Core #MMPMID25673286 Pócsai K; Kálmán M J Histochem Cytochem 2015[May]; 63 (5): 367-83 PMID25673286show ga The subfornical organ (SFO) is a circumventricular organ with a chemosensitive function, and its vessels have no blood-brain barrier. Our study investigated the glial and vascular components in the SFO to determine whether their distributions indicate subdivisions, how to characterize the vessels and how to demarcate the SFO. To this end, we investigated glial markers (GFAP, glutamine synthetase, S100) and other markers, including vimentin and nestin (immature glia), laminin (basal lamina), ?-dystroglycan (glio-vascular connections), and aquaporin 4 (glial water channels). We determined that the ?shell? of the SFO was marked by immunoreactivity for S100, GFAP and aquaporin 4. Nestin immunoreactivity was characteristic of the ?core?. Vimentin was almost evenly distributed. Glutamine synthetase immunoreactivity occurred in the shell but its expression was sparse. Vessels in the core were decorated with laminin but showed a discontinuous expression of aquaporin 4. Vimentin and GFAP staining was usually in separate glial elements, which may be related to their functional differences. Similar to other vessels in the brain, ?-dystroglycan was detected along the shell vessels but laminin was not. The gradual disappearance of the laminin immunopositivity was attributed to the gradual disappearance of the perivascular space. Thus, our findings suggest that the shell and core glio-vascular structures are adapted to different sensory functions: osmoperception and the perception of circulating peptides, respectively. äGlial and Perivascular Structures in the Subfornical Organ: Distinguis(epmc).pdf DeepDyve Pubget Overpricing