Calbindin D28k expression in immunohistochemically identified Renshaw cells
DOUBLE immunofluorescence was utilized to determine whether Renshaw cells contain calbindin D28k immunoreactivity. Renshaw cells were identified by their characteristic expression patterns of gephyrin immunoreactivity in sections of rat and cat lumbar spinal cord. In the rat, all neurons classified...
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Veröffentlicht in: | Neuroreport 1998-08, Vol.9 (11), p.2657-2661 |
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description | DOUBLE immunofluorescence was utilized to determine whether Renshaw cells contain calbindin D28k immunoreactivity. Renshaw cells were identified by their characteristic expression patterns of gephyrin immunoreactivity in sections of rat and cat lumbar spinal cord. In the rat, all neurons classified as Renshaw cells (n = 487) also contained calbindin D28k-immunoreactivity, and all calbindin D28k-immunoreactive cells located in the ventral-most region of lamina VII expressed the characteristic gephyrin labeling and morphology of Renshaw cells. In the cat, fewer than half of the Renshaw cells (47%; n = 128) were double-labeled. In both species, occasional calbindin D28k-immunoreactive Renshaw cells were identified within motor nuclei in lamina IX. The distinctive immunolabeling of Renshaw cells allowed us to estimate that there are about 250 Renshaw cells in each ventral horn of the fourth lumbar segment of rat spinal cord, and about 750 cells per ventral horn in the L6 segment of the cat. We conclude that the functional properties of Renshaw cells, including their ability to fire action potentials at high rates, likely require specific homeostatic mechanisms including strong intracellular calcium buffering, the precise mechanisms of which may vary between species. |
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Fyffe, Robert E</creator><creatorcontrib>Carr, Patrick A ; Alvarez, Francisco J ; Leman, Elizabeth A ; W. Fyffe, Robert E</creatorcontrib><description>DOUBLE immunofluorescence was utilized to determine whether Renshaw cells contain calbindin D28k immunoreactivity. Renshaw cells were identified by their characteristic expression patterns of gephyrin immunoreactivity in sections of rat and cat lumbar spinal cord. In the rat, all neurons classified as Renshaw cells (n = 487) also contained calbindin D28k-immunoreactivity, and all calbindin D28k-immunoreactive cells located in the ventral-most region of lamina VII expressed the characteristic gephyrin labeling and morphology of Renshaw cells. In the cat, fewer than half of the Renshaw cells (47%; n = 128) were double-labeled. In both species, occasional calbindin D28k-immunoreactive Renshaw cells were identified within motor nuclei in lamina IX. The distinctive immunolabeling of Renshaw cells allowed us to estimate that there are about 250 Renshaw cells in each ventral horn of the fourth lumbar segment of rat spinal cord, and about 750 cells per ventral horn in the L6 segment of the cat. We conclude that the functional properties of Renshaw cells, including their ability to fire action potentials at high rates, likely require specific homeostatic mechanisms including strong intracellular calcium buffering, the precise mechanisms of which may vary between species.</description><identifier>ISSN: 0959-4965</identifier><identifier>EISSN: 1473-558X</identifier><identifier>DOI: 10.1097/00001756-199808030-00043</identifier><identifier>PMID: 9721951</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott-Raven Publishers</publisher><subject>Anatomy ; Animals ; Biological and medical sciences ; Calbindin 1 ; Calbindins ; Carrier Proteins - biosynthesis ; Cats ; Central nervous system ; Fundamental and applied biological sciences. Psychology ; Immunohistochemistry ; Interneurons - metabolism ; Male ; Membrane Proteins - biosynthesis ; Nerve Tissue Proteins - biosynthesis ; Rats ; Rats, Sprague-Dawley ; S100 Calcium Binding Protein G - biosynthesis ; Spinal Cord - cytology ; Spinal Cord - metabolism ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroreport, 1998-08, Vol.9 (11), p.2657-2661</ispartof><rights>Lippincott-Raven Publishers.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4153-f56ed2489dae5d52a605160faf4205f4b3fc3f68e16ecd36a6e6d081a4de98183</citedby><cites>FETCH-LOGICAL-c4153-f56ed2489dae5d52a605160faf4205f4b3fc3f68e16ecd36a6e6d081a4de98183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1603863$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9721951$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carr, Patrick A</creatorcontrib><creatorcontrib>Alvarez, Francisco J</creatorcontrib><creatorcontrib>Leman, Elizabeth A</creatorcontrib><creatorcontrib>W. Fyffe, Robert E</creatorcontrib><title>Calbindin D28k expression in immunohistochemically identified Renshaw cells</title><title>Neuroreport</title><addtitle>Neuroreport</addtitle><description>DOUBLE immunofluorescence was utilized to determine whether Renshaw cells contain calbindin D28k immunoreactivity. Renshaw cells were identified by their characteristic expression patterns of gephyrin immunoreactivity in sections of rat and cat lumbar spinal cord. In the rat, all neurons classified as Renshaw cells (n = 487) also contained calbindin D28k-immunoreactivity, and all calbindin D28k-immunoreactive cells located in the ventral-most region of lamina VII expressed the characteristic gephyrin labeling and morphology of Renshaw cells. In the cat, fewer than half of the Renshaw cells (47%; n = 128) were double-labeled. In both species, occasional calbindin D28k-immunoreactive Renshaw cells were identified within motor nuclei in lamina IX. The distinctive immunolabeling of Renshaw cells allowed us to estimate that there are about 250 Renshaw cells in each ventral horn of the fourth lumbar segment of rat spinal cord, and about 750 cells per ventral horn in the L6 segment of the cat. We conclude that the functional properties of Renshaw cells, including their ability to fire action potentials at high rates, likely require specific homeostatic mechanisms including strong intracellular calcium buffering, the precise mechanisms of which may vary between species.</description><subject>Anatomy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Calbindin 1</subject><subject>Calbindins</subject><subject>Carrier Proteins - biosynthesis</subject><subject>Cats</subject><subject>Central nervous system</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Immunohistochemistry</subject><subject>Interneurons - metabolism</subject><subject>Male</subject><subject>Membrane Proteins - biosynthesis</subject><subject>Nerve Tissue Proteins - biosynthesis</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>S100 Calcium Binding Protein G - biosynthesis</subject><subject>Spinal Cord - cytology</subject><subject>Spinal Cord - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0959-4965</issn><issn>1473-558X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVoSDeb_ISAD6U3pxrrw9KxbD8SGiiEFnoTWmuElcj2VrLZ7r-vt7tJTyFzGZh5553hGUIKoNdAdf2BzgG1kCVoraiijJZzhbMTsgBes1II9esNWVAtdMm1FG_Jec4Ps0RTUGfkTNcVaAEL8m1l4zr0LvTFp0o9FvhnkzDnMPTFXApdN_VDG_I4NC12obEx7orgsB-DD-iKe-xza7dFgzHmC3Lqbcx4ecxL8vPL5x-rm_Lu-9fb1ce7suEgWOmFRFdxpZ1F4URlJRUgqbeeV1R4vma-YV4qBImNY9JKlI4qsNyhVqDYkrw_-G7S8HvCPJou5P0FtsdhyqZmSmlB4VUh1EBBzDctiToImzTknNCbTQqdTTsD1OyBmyfg5hm4-Qd8Hr067pjWHbrnwSPhuf_u2Ld5xueT7ZuQ__tLypTc2_CDbDvEEVN-jNMWk2nRxrE1L72b_QXRuZfi</recordid><startdate>19980803</startdate><enddate>19980803</enddate><creator>Carr, Patrick A</creator><creator>Alvarez, Francisco J</creator><creator>Leman, Elizabeth A</creator><creator>W. Fyffe, Robert E</creator><general>Lippincott-Raven Publishers</general><general>Lippincott Williams and Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>19980803</creationdate><title>Calbindin D28k expression in immunohistochemically identified Renshaw cells</title><author>Carr, Patrick A ; Alvarez, Francisco J ; Leman, Elizabeth A ; W. Fyffe, Robert E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4153-f56ed2489dae5d52a605160faf4205f4b3fc3f68e16ecd36a6e6d081a4de98183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Anatomy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Calbindin 1</topic><topic>Calbindins</topic><topic>Carrier Proteins - biosynthesis</topic><topic>Cats</topic><topic>Central nervous system</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Immunohistochemistry</topic><topic>Interneurons - metabolism</topic><topic>Male</topic><topic>Membrane Proteins - biosynthesis</topic><topic>Nerve Tissue Proteins - biosynthesis</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>S100 Calcium Binding Protein G - biosynthesis</topic><topic>Spinal Cord - cytology</topic><topic>Spinal Cord - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carr, Patrick A</creatorcontrib><creatorcontrib>Alvarez, Francisco J</creatorcontrib><creatorcontrib>Leman, Elizabeth A</creatorcontrib><creatorcontrib>W. Fyffe, Robert E</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroreport</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carr, Patrick A</au><au>Alvarez, Francisco J</au><au>Leman, Elizabeth A</au><au>W. Fyffe, Robert E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Calbindin D28k expression in immunohistochemically identified Renshaw cells</atitle><jtitle>Neuroreport</jtitle><addtitle>Neuroreport</addtitle><date>1998-08-03</date><risdate>1998</risdate><volume>9</volume><issue>11</issue><spage>2657</spage><epage>2661</epage><pages>2657-2661</pages><issn>0959-4965</issn><eissn>1473-558X</eissn><abstract>DOUBLE immunofluorescence was utilized to determine whether Renshaw cells contain calbindin D28k immunoreactivity. Renshaw cells were identified by their characteristic expression patterns of gephyrin immunoreactivity in sections of rat and cat lumbar spinal cord. In the rat, all neurons classified as Renshaw cells (n = 487) also contained calbindin D28k-immunoreactivity, and all calbindin D28k-immunoreactive cells located in the ventral-most region of lamina VII expressed the characteristic gephyrin labeling and morphology of Renshaw cells. In the cat, fewer than half of the Renshaw cells (47%; n = 128) were double-labeled. In both species, occasional calbindin D28k-immunoreactive Renshaw cells were identified within motor nuclei in lamina IX. The distinctive immunolabeling of Renshaw cells allowed us to estimate that there are about 250 Renshaw cells in each ventral horn of the fourth lumbar segment of rat spinal cord, and about 750 cells per ventral horn in the L6 segment of the cat. We conclude that the functional properties of Renshaw cells, including their ability to fire action potentials at high rates, likely require specific homeostatic mechanisms including strong intracellular calcium buffering, the precise mechanisms of which may vary between species.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>9721951</pmid><doi>10.1097/00001756-199808030-00043</doi><tpages>5</tpages></addata></record> |
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subjects | Anatomy Animals Biological and medical sciences Calbindin 1 Calbindins Carrier Proteins - biosynthesis Cats Central nervous system Fundamental and applied biological sciences. Psychology Immunohistochemistry Interneurons - metabolism Male Membrane Proteins - biosynthesis Nerve Tissue Proteins - biosynthesis Rats Rats, Sprague-Dawley S100 Calcium Binding Protein G - biosynthesis Spinal Cord - cytology Spinal Cord - metabolism Vertebrates: nervous system and sense organs |
title | Calbindin D28k expression in immunohistochemically identified Renshaw cells |
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