Development of Immune Hyperinnervation in NGF-Transgenic Mice
Sympathetic innervation of lymphoid tissues is localized to specific tissue compartments, but little is known of the “factors” that are important in establishing this pattern during development. Numerous studies have shown interactions of nerve growth factor (NGF) with the immune system, which may i...
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Veröffentlicht in: | Experimental neurology 1998-01, Vol.149 (1), p.209-220 |
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description | Sympathetic innervation of lymphoid tissues is localized to specific tissue compartments, but little is known of the “factors” that are important in establishing this pattern during development. Numerous studies have shown interactions of nerve growth factor (NGF) with the immune system, which may include modulation of immune innervation. We previously have shown that NGF transgenic mice, which overexpress NGF in skin and not immune tissues, have a dramatic hyperinnervation of splenic marginal zone and peripheral lymph node medulla and capsule. The purpose of the current studies was to determine if the presence of elevated NGF would alter immune system development and the process of sympathetic ingrowth. The results show that the splenic innervation in NGF transgenics gradually diverged from controls during the first two postnatal weeks, with the greatest change occurring between postnatal days 13 and 16 when the splenic organization was reaching the adult pattern. In contrast, the peripheral lymph nodes were hyperinnervated at an earlier age. Mesenteric lymph nodes never diverged from the normal pattern. NGF levels in transgenic spleen were much higher than controls at postnatal days 1 and 2, when little innervation was present, and declined as the tissue matured, possibly because of NGF uptake by the ingrowing sympathetic fibers. This suggests that immune tissues are capable of concentrating NGF, which in turn may modulate the level of innervation by the sympathetic nervous system. |
doi_str_mv | 10.1006/exnr.1997.6711 |
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Numerous studies have shown interactions of nerve growth factor (NGF) with the immune system, which may include modulation of immune innervation. We previously have shown that NGF transgenic mice, which overexpress NGF in skin and not immune tissues, have a dramatic hyperinnervation of splenic marginal zone and peripheral lymph node medulla and capsule. The purpose of the current studies was to determine if the presence of elevated NGF would alter immune system development and the process of sympathetic ingrowth. The results show that the splenic innervation in NGF transgenics gradually diverged from controls during the first two postnatal weeks, with the greatest change occurring between postnatal days 13 and 16 when the splenic organization was reaching the adult pattern. In contrast, the peripheral lymph nodes were hyperinnervated at an earlier age. Mesenteric lymph nodes never diverged from the normal pattern. NGF levels in transgenic spleen were much higher than controls at postnatal days 1 and 2, when little innervation was present, and declined as the tissue matured, possibly because of NGF uptake by the ingrowing sympathetic fibers. This suggests that immune tissues are capable of concentrating NGF, which in turn may modulate the level of innervation by the sympathetic nervous system.</description><identifier>ISSN: 0014-4886</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1006/exnr.1997.6711</identifier><identifier>PMID: 9454630</identifier><identifier>CODEN: EXNEAC</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Animals ; Animals, Newborn - growth & development ; Biological and medical sciences ; ELISA ; Fundamental and applied biological sciences. Psychology ; Immune System - growth & development ; Immune System - innervation ; liver ; lymph node ; Lymph Nodes - growth & development ; Lymph Nodes - innervation ; Mice ; Mice, Transgenic - genetics ; nerve growth factor ; Nerve Growth Factors - genetics ; Nerve Growth Factors - metabolism ; Nervous System Diseases - genetics ; norepinephrine ; Norepinephrine - metabolism ; Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ ; spleen ; Spleen - growth & development ; Spleen - innervation ; Spleen - metabolism ; sympathetic nervous system ; Sympathetic Nervous System - growth & development ; Sympathetic Nervous System - metabolism ; Sympathetic Nervous System - physiopathology ; Vertebrates: nervous system and sense organs</subject><ispartof>Experimental neurology, 1998-01, Vol.149 (1), p.209-220</ispartof><rights>1998 Academic Press</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-f4e1872ba445ae81f0c968a0186b027517995962ed87f3e4104b7ecc84aed8ac3</citedby><cites>FETCH-LOGICAL-c368t-f4e1872ba445ae81f0c968a0186b027517995962ed87f3e4104b7ecc84aed8ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/exnr.1997.6711$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2151350$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9454630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carlson, Sonia L.</creatorcontrib><creatorcontrib>Johnson, Sonia</creatorcontrib><creatorcontrib>Parrish, Mark E.</creatorcontrib><creatorcontrib>Cass, Wayne A.</creatorcontrib><title>Development of Immune Hyperinnervation in NGF-Transgenic Mice</title><title>Experimental neurology</title><addtitle>Exp Neurol</addtitle><description>Sympathetic innervation of lymphoid tissues is localized to specific tissue compartments, but little is known of the “factors” that are important in establishing this pattern during development. Numerous studies have shown interactions of nerve growth factor (NGF) with the immune system, which may include modulation of immune innervation. We previously have shown that NGF transgenic mice, which overexpress NGF in skin and not immune tissues, have a dramatic hyperinnervation of splenic marginal zone and peripheral lymph node medulla and capsule. The purpose of the current studies was to determine if the presence of elevated NGF would alter immune system development and the process of sympathetic ingrowth. The results show that the splenic innervation in NGF transgenics gradually diverged from controls during the first two postnatal weeks, with the greatest change occurring between postnatal days 13 and 16 when the splenic organization was reaching the adult pattern. In contrast, the peripheral lymph nodes were hyperinnervated at an earlier age. Mesenteric lymph nodes never diverged from the normal pattern. NGF levels in transgenic spleen were much higher than controls at postnatal days 1 and 2, when little innervation was present, and declined as the tissue matured, possibly because of NGF uptake by the ingrowing sympathetic fibers. This suggests that immune tissues are capable of concentrating NGF, which in turn may modulate the level of innervation by the sympathetic nervous system.</description><subject>Animals</subject><subject>Animals, Newborn - growth & development</subject><subject>Biological and medical sciences</subject><subject>ELISA</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Immune System - growth & development</subject><subject>Immune System - innervation</subject><subject>liver</subject><subject>lymph node</subject><subject>Lymph Nodes - growth & development</subject><subject>Lymph Nodes - innervation</subject><subject>Mice</subject><subject>Mice, Transgenic - genetics</subject><subject>nerve growth factor</subject><subject>Nerve Growth Factors - genetics</subject><subject>Nerve Growth Factors - metabolism</subject><subject>Nervous System Diseases - genetics</subject><subject>norepinephrine</subject><subject>Norepinephrine - metabolism</subject><subject>Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ</subject><subject>spleen</subject><subject>Spleen - growth & development</subject><subject>Spleen - innervation</subject><subject>Spleen - metabolism</subject><subject>sympathetic nervous system</subject><subject>Sympathetic Nervous System - growth & development</subject><subject>Sympathetic Nervous System - metabolism</subject><subject>Sympathetic Nervous System - physiopathology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0014-4886</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kLtPwzAQhy0EgvJY2ZAyILaUu8SJ7YEBlafEY4HZct0LMkqcYicV_e9J1Kob00l33_109zF2jjBFgPKafn2YolJiWgrEPTZBUJBmPId9NgFAnnIpyyN2HOM3ACieiUN2qHjByxwm7OaOVlS3y4Z8l7RV8tw0vafkab2k4LynsDKda33ifPL2-JB-BOPjF3lnk1dn6ZQdVKaOdLatJ-zz4f5j9pS-vD8-z25fUpuXsksrTihFNjecF4YkVmBVKQ2gLOeQiQKFUoUqM1pIUeXEEfhckLWSm6FlbH7Crja5y9D-9BQ73bhoqa6Np7aPWgxxqAAHcLoBbWhjDFTpZXCNCWuNoEdfevSlR1969DUsXGyT-3lDix2-FTTML7dzE62pq-F_6-IOy7DAvBgxucFosLByFHS0jrylhQtkO71o3X8X_AEuRoWO</recordid><startdate>199801</startdate><enddate>199801</enddate><creator>Carlson, Sonia L.</creator><creator>Johnson, Sonia</creator><creator>Parrish, Mark E.</creator><creator>Cass, Wayne A.</creator><general>Elsevier Inc</general><general>Elsevier</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>7X8</scope></search><sort><creationdate>199801</creationdate><title>Development of Immune Hyperinnervation in NGF-Transgenic Mice</title><author>Carlson, Sonia L. ; Johnson, Sonia ; Parrish, Mark E. ; Cass, Wayne A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-f4e1872ba445ae81f0c968a0186b027517995962ed87f3e4104b7ecc84aed8ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Animals, Newborn - growth & development</topic><topic>Biological and medical sciences</topic><topic>ELISA</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Immune System - growth & development</topic><topic>Immune System - innervation</topic><topic>liver</topic><topic>lymph node</topic><topic>Lymph Nodes - growth & development</topic><topic>Lymph Nodes - innervation</topic><topic>Mice</topic><topic>Mice, Transgenic - genetics</topic><topic>nerve growth factor</topic><topic>Nerve Growth Factors - genetics</topic><topic>Nerve Growth Factors - metabolism</topic><topic>Nervous System Diseases - genetics</topic><topic>norepinephrine</topic><topic>Norepinephrine - metabolism</topic><topic>Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ</topic><topic>spleen</topic><topic>Spleen - growth & development</topic><topic>Spleen - innervation</topic><topic>Spleen - metabolism</topic><topic>sympathetic nervous system</topic><topic>Sympathetic Nervous System - growth & development</topic><topic>Sympathetic Nervous System - metabolism</topic><topic>Sympathetic Nervous System - physiopathology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carlson, Sonia L.</creatorcontrib><creatorcontrib>Johnson, Sonia</creatorcontrib><creatorcontrib>Parrish, Mark E.</creatorcontrib><creatorcontrib>Cass, Wayne A.</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>MEDLINE - Academic</collection><jtitle>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carlson, Sonia L.</au><au>Johnson, Sonia</au><au>Parrish, Mark E.</au><au>Cass, Wayne A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of Immune Hyperinnervation in NGF-Transgenic Mice</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>1998-01</date><risdate>1998</risdate><volume>149</volume><issue>1</issue><spage>209</spage><epage>220</epage><pages>209-220</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><coden>EXNEAC</coden><abstract>Sympathetic innervation of lymphoid tissues is localized to specific tissue compartments, but little is known of the “factors” that are important in establishing this pattern during development. Numerous studies have shown interactions of nerve growth factor (NGF) with the immune system, which may include modulation of immune innervation. We previously have shown that NGF transgenic mice, which overexpress NGF in skin and not immune tissues, have a dramatic hyperinnervation of splenic marginal zone and peripheral lymph node medulla and capsule. The purpose of the current studies was to determine if the presence of elevated NGF would alter immune system development and the process of sympathetic ingrowth. The results show that the splenic innervation in NGF transgenics gradually diverged from controls during the first two postnatal weeks, with the greatest change occurring between postnatal days 13 and 16 when the splenic organization was reaching the adult pattern. In contrast, the peripheral lymph nodes were hyperinnervated at an earlier age. Mesenteric lymph nodes never diverged from the normal pattern. NGF levels in transgenic spleen were much higher than controls at postnatal days 1 and 2, when little innervation was present, and declined as the tissue matured, possibly because of NGF uptake by the ingrowing sympathetic fibers. This suggests that immune tissues are capable of concentrating NGF, which in turn may modulate the level of innervation by the sympathetic nervous system.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>9454630</pmid><doi>10.1006/exnr.1997.6711</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Animals, Newborn - growth & development Biological and medical sciences ELISA Fundamental and applied biological sciences. Psychology Immune System - growth & development Immune System - innervation liver lymph node Lymph Nodes - growth & development Lymph Nodes - innervation Mice Mice, Transgenic - genetics nerve growth factor Nerve Growth Factors - genetics Nerve Growth Factors - metabolism Nervous System Diseases - genetics norepinephrine Norepinephrine - metabolism Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ spleen Spleen - growth & development Spleen - innervation Spleen - metabolism sympathetic nervous system Sympathetic Nervous System - growth & development Sympathetic Nervous System - metabolism Sympathetic Nervous System - physiopathology Vertebrates: nervous system and sense organs |
title | Development of Immune Hyperinnervation in NGF-Transgenic Mice |
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