Neuronal characteristics in embryonic renal stroma
The metanephric mesenchyme is considered a homogeneous population of predetermined, but pluripotent cells with a nephrogenic bias. By an inductive stimulus, the mesenchyme is programmed to differentiate into the various epithelial phenotypes of the secretory nephron. A fraction of the mesenchymal ce...
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Veröffentlicht in: | The International journal of developmental biology 1994-03, Vol.38 (1), p.77-84 |
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description | The metanephric mesenchyme is considered a homogeneous population of predetermined, but pluripotent cells with a nephrogenic bias. By an inductive stimulus, the mesenchyme is programmed to differentiate into the various epithelial phenotypes of the secretory nephron. A fraction of the mesenchymal cells, however, remains in the interstitium between the nephrons and differentiates into spindle-shaped, clear-cytoplasmic renal stroma. We have analyzed the molecular nature of these cells in order to discover the specific cell types that could be involved in the morphogenetic processes during kidney differentiation. In situ hybridization reveals neurofilament light protein mRNA, and immunohistology shows neurofilament light and medium proteins in the stromal cells around kidney tubules. By immunohistochemistry these peritubular stromal cells can be distinguished from the neuronal cells of the renal microganglion: the peritubular stromal cells are neurofilament-positive but L1 neural cell adhesion protein-negative, whereas the neuronal cells with axonal extension are both neurofilament-positive and L1 neural cell adhesion protein-positive. Proliferation index of the stromal cells was low as compared to tubular cells, as shown by bromodeoxyuridine incorporation. |
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By an inductive stimulus, the mesenchyme is programmed to differentiate into the various epithelial phenotypes of the secretory nephron. A fraction of the mesenchymal cells, however, remains in the interstitium between the nephrons and differentiates into spindle-shaped, clear-cytoplasmic renal stroma. We have analyzed the molecular nature of these cells in order to discover the specific cell types that could be involved in the morphogenetic processes during kidney differentiation. In situ hybridization reveals neurofilament light protein mRNA, and immunohistology shows neurofilament light and medium proteins in the stromal cells around kidney tubules. By immunohistochemistry these peritubular stromal cells can be distinguished from the neuronal cells of the renal microganglion: the peritubular stromal cells are neurofilament-positive but L1 neural cell adhesion protein-negative, whereas the neuronal cells with axonal extension are both neurofilament-positive and L1 neural cell adhesion protein-positive. Proliferation index of the stromal cells was low as compared to tubular cells, as shown by bromodeoxyuridine incorporation.</description><identifier>ISSN: 0214-6282</identifier><identifier>EISSN: 1696-3547</identifier><identifier>PMID: 8074998</identifier><language>eng</language><publisher>Bilbao: University of the Basque Country Press</publisher><subject>Animals ; Biological and medical sciences ; Cell Adhesion Molecules, Neuronal - analysis ; Cell Adhesion Molecules, Neuronal - biosynthesis ; Cell Differentiation ; Embryology: invertebrates and vertebrates. Teratology ; Epithelial Cells ; Epithelium - physiology ; Female ; Fundamental and applied biological sciences. Psychology ; In Situ Hybridization ; Kidney - embryology ; Kidney - innervation ; Male ; Mice ; Mice, Inbred CBA ; Mice, Inbred Strains ; Morphogenesis ; Neurofilament Proteins - biosynthesis ; Neurons - cytology ; Neurons - physiology ; Organogenesis. Fetal development ; Organogenesis. Physiological fonctions ; Phenotype ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - analysis ; RNA, Messenger - biosynthesis ; Stem Cells - cytology ; Stem Cells - physiology</subject><ispartof>The International journal of developmental biology, 1994-03, Vol.38 (1), p.77-84</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4079630$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8074998$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SAINIO, K</creatorcontrib><creatorcontrib>NONCLERCQ, D</creatorcontrib><creatorcontrib>SAARMA, M</creatorcontrib><creatorcontrib>PALGI, J</creatorcontrib><creatorcontrib>SAXEN, L</creatorcontrib><creatorcontrib>SARIOLA, H</creatorcontrib><title>Neuronal characteristics in embryonic renal stroma</title><title>The International journal of developmental biology</title><addtitle>Int J Dev Biol</addtitle><description>The metanephric mesenchyme is considered a homogeneous population of predetermined, but pluripotent cells with a nephrogenic bias. By an inductive stimulus, the mesenchyme is programmed to differentiate into the various epithelial phenotypes of the secretory nephron. A fraction of the mesenchymal cells, however, remains in the interstitium between the nephrons and differentiates into spindle-shaped, clear-cytoplasmic renal stroma. We have analyzed the molecular nature of these cells in order to discover the specific cell types that could be involved in the morphogenetic processes during kidney differentiation. In situ hybridization reveals neurofilament light protein mRNA, and immunohistology shows neurofilament light and medium proteins in the stromal cells around kidney tubules. By immunohistochemistry these peritubular stromal cells can be distinguished from the neuronal cells of the renal microganglion: the peritubular stromal cells are neurofilament-positive but L1 neural cell adhesion protein-negative, whereas the neuronal cells with axonal extension are both neurofilament-positive and L1 neural cell adhesion protein-positive. Proliferation index of the stromal cells was low as compared to tubular cells, as shown by bromodeoxyuridine incorporation.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Adhesion Molecules, Neuronal - analysis</subject><subject>Cell Adhesion Molecules, Neuronal - biosynthesis</subject><subject>Cell Differentiation</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Epithelial Cells</subject><subject>Epithelium - physiology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>In Situ Hybridization</subject><subject>Kidney - embryology</subject><subject>Kidney - innervation</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred CBA</subject><subject>Mice, Inbred Strains</subject><subject>Morphogenesis</subject><subject>Neurofilament Proteins - biosynthesis</subject><subject>Neurons - cytology</subject><subject>Neurons - physiology</subject><subject>Organogenesis. Fetal development</subject><subject>Organogenesis. Physiological fonctions</subject><subject>Phenotype</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - physiology</subject><issn>0214-6282</issn><issn>1696-3547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9j01LxDAQhoMoa63-BKEH8VZI852jLOoKi170XCZpgpF-mbSH_fdGLJ6Gl-ed4ZkzVDRCi5pyJs9RgUnDakEUuURXKX3hnLGSO7RTWDKtVYHIq1vjNEJf2U-IYBcXQ1qCTVUYKzeYeJrGYKvofitpidMA1-jCQ5_czTZL9PH0-L4_1Me355f9w7GeCeVLzRgnXdMBCLAeODXcA9GCGiZ903HDbObeKpUjdAZnTaq1zuZOUeY8LdH93905Tt-rS0s7hGRd38PopjW1UgjFed4q0e1WXM3gunaOYYB4arcnM7_bOCQLvY8w2pD-awzLrIXpD4ItW1g</recordid><startdate>19940301</startdate><enddate>19940301</enddate><creator>SAINIO, K</creator><creator>NONCLERCQ, D</creator><creator>SAARMA, M</creator><creator>PALGI, J</creator><creator>SAXEN, L</creator><creator>SARIOLA, H</creator><general>University of the Basque Country Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19940301</creationdate><title>Neuronal characteristics in embryonic renal stroma</title><author>SAINIO, K ; NONCLERCQ, D ; SAARMA, M ; PALGI, J ; SAXEN, L ; SARIOLA, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p235t-4452d1daa6acfa53b5fa2963b47f1d5b4c52dfc887f1adb06283999354e834ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Adhesion Molecules, Neuronal - analysis</topic><topic>Cell Adhesion Molecules, Neuronal - biosynthesis</topic><topic>Cell Differentiation</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Epithelial Cells</topic><topic>Epithelium - physiology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>In Situ Hybridization</topic><topic>Kidney - embryology</topic><topic>Kidney - innervation</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred CBA</topic><topic>Mice, Inbred Strains</topic><topic>Morphogenesis</topic><topic>Neurofilament Proteins - biosynthesis</topic><topic>Neurons - cytology</topic><topic>Neurons - physiology</topic><topic>Organogenesis. Fetal development</topic><topic>Organogenesis. Physiological fonctions</topic><topic>Phenotype</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SAINIO, K</creatorcontrib><creatorcontrib>NONCLERCQ, D</creatorcontrib><creatorcontrib>SAARMA, M</creatorcontrib><creatorcontrib>PALGI, J</creatorcontrib><creatorcontrib>SAXEN, L</creatorcontrib><creatorcontrib>SARIOLA, H</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>MEDLINE - Academic</collection><jtitle>The International journal of developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SAINIO, K</au><au>NONCLERCQ, D</au><au>SAARMA, M</au><au>PALGI, J</au><au>SAXEN, L</au><au>SARIOLA, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuronal characteristics in embryonic renal stroma</atitle><jtitle>The International journal of developmental biology</jtitle><addtitle>Int J Dev Biol</addtitle><date>1994-03-01</date><risdate>1994</risdate><volume>38</volume><issue>1</issue><spage>77</spage><epage>84</epage><pages>77-84</pages><issn>0214-6282</issn><eissn>1696-3547</eissn><abstract>The metanephric mesenchyme is considered a homogeneous population of predetermined, but pluripotent cells with a nephrogenic bias. By an inductive stimulus, the mesenchyme is programmed to differentiate into the various epithelial phenotypes of the secretory nephron. A fraction of the mesenchymal cells, however, remains in the interstitium between the nephrons and differentiates into spindle-shaped, clear-cytoplasmic renal stroma. We have analyzed the molecular nature of these cells in order to discover the specific cell types that could be involved in the morphogenetic processes during kidney differentiation. In situ hybridization reveals neurofilament light protein mRNA, and immunohistology shows neurofilament light and medium proteins in the stromal cells around kidney tubules. By immunohistochemistry these peritubular stromal cells can be distinguished from the neuronal cells of the renal microganglion: the peritubular stromal cells are neurofilament-positive but L1 neural cell adhesion protein-negative, whereas the neuronal cells with axonal extension are both neurofilament-positive and L1 neural cell adhesion protein-positive. Proliferation index of the stromal cells was low as compared to tubular cells, as shown by bromodeoxyuridine incorporation.</abstract><cop>Bilbao</cop><pub>University of the Basque Country Press</pub><pmid>8074998</pmid><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cell Adhesion Molecules, Neuronal - analysis Cell Adhesion Molecules, Neuronal - biosynthesis Cell Differentiation Embryology: invertebrates and vertebrates. Teratology Epithelial Cells Epithelium - physiology Female Fundamental and applied biological sciences. Psychology In Situ Hybridization Kidney - embryology Kidney - innervation Male Mice Mice, Inbred CBA Mice, Inbred Strains Morphogenesis Neurofilament Proteins - biosynthesis Neurons - cytology Neurons - physiology Organogenesis. Fetal development Organogenesis. Physiological fonctions Phenotype Rats Rats, Sprague-Dawley RNA, Messenger - analysis RNA, Messenger - biosynthesis Stem Cells - cytology Stem Cells - physiology |
title | Neuronal characteristics in embryonic renal stroma |
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