Interleukin-4 down-regulates MHC class II antigens on cultured rat astrocytes

Mammalian cerebral astrocytes can be brought to express major histocompatibility complex (MHC) class II molecules upon appropriate stimulation. It is well established that this expression is subject to modulation by several neurotransmitters and cytokines. We show that the low, basal expression of M...

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Veröffentlicht in:Glia 1996-06, Vol.17 (2), p.175-179
Hauptverfasser: Morga, Eleonora, Heuschling, Paul
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description Mammalian cerebral astrocytes can be brought to express major histocompatibility complex (MHC) class II molecules upon appropriate stimulation. It is well established that this expression is subject to modulation by several neurotransmitters and cytokines. We show that the low, basal expression of MHC class II antigens on cultured rat astrocytes is concentration‐dependently down‐regulated by low concentrations of interleukin‐4 (IL‐4), reaching maximal inhibition at 10 U/ml. The higher, γ‐IFN‐induced, expression of class II molecules is also decreased by increasing concentrations of IL‐4, significant effects being already observed at 5 U/ml. Since the cAMP as well as the nitric oxide dependent cGMP pathway have previously been shown to mediate an inhibition on astroglial MHC class II expression, we measured the intra‐cellular content of cyclic nucleotides after stimulation with IL‐4. No rise in cAMP or cGMP is detected. Similarly, IL‐4 does not affect the induced synthesis of nitric oxide radicals. Since MHC class II expression is a critical step in many regulatory processes of the cellular immune reaction, IL‐4, via its activity on astroglial cells, emerges as an important modulator of immunological activities in the central nervous system. © 1996 Wiley‐Liss, Inc.
doi_str_mv 10.1002/(SICI)1098-1136(199606)17:2<175::AID-GLIA9>3.0.CO;2-1
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It is well established that this expression is subject to modulation by several neurotransmitters and cytokines. We show that the low, basal expression of MHC class II antigens on cultured rat astrocytes is concentration‐dependently down‐regulated by low concentrations of interleukin‐4 (IL‐4), reaching maximal inhibition at 10 U/ml. The higher, γ‐IFN‐induced, expression of class II molecules is also decreased by increasing concentrations of IL‐4, significant effects being already observed at 5 U/ml. Since the cAMP as well as the nitric oxide dependent cGMP pathway have previously been shown to mediate an inhibition on astroglial MHC class II expression, we measured the intra‐cellular content of cyclic nucleotides after stimulation with IL‐4. No rise in cAMP or cGMP is detected. Similarly, IL‐4 does not affect the induced synthesis of nitric oxide radicals. Since MHC class II expression is a critical step in many regulatory processes of the cellular immune reaction, IL‐4, via its activity on astroglial cells, emerges as an important modulator of immunological activities in the central nervous system. © 1996 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Astrocytes - metabolism</subject><subject>Biological and medical sciences</subject><subject>cAMP</subject><subject>Cells, Cultured - metabolism</subject><subject>cGMP</subject><subject>Down-Regulation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gamma-interferon</subject><subject>Histocompatibility Antigens Class II - metabolism</subject><subject>Interleukin-4 - metabolism</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>major histocompatibility complex</subject><subject>nitric oxide</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Time Factors</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVtr3DAQhU1pSbdpf0LBD6UkD9pqdLW3F1i87caw6RZ6C3kZFFsOTrx2Ktmk--9r14tfWggCCc2c-TjMCYL3QOdAKXtz8jVN0lOgcUQAuDqBOFZUnYJesHeg5WKxTFdkvUmX8Qc-p_Nk-5YReBTMponHwYxGsSAgYngaPPP-hlLoP_ooOIq0VjISs-A8rVvrKtvdljURYd7c18TZ664yrfXh-VkSZpXxPkzT0NRteW1rHzZ1mHVV2zmbh860ofGta7J9P_A8eFKYytsXh_c4-P7p47fkjGy26zRZbkgmFMSk4FRCrrhgFnhxxRXVSlOZFyIzUVTIKDeRlixXRnEO0lBthS20AIhzpkXBj4PXI_fONb8661vclT6zVWVq23QedcSGIx4UgpQRBwV8cpq5xntnC7xz5c64PQLFIQ_EIQ8ctovDdnHMA0Ej6y-J2OeBf_NAjhST7VDvuS8PBrqrnc0n6iGAvv_q0Dc-M1XhTJ2VfpJxYBIo62U_Rtl9Wdn9P94esPY_Z2OhB5MRXPrW_p7Axt2i0ryf_fl5jfzLhVytLi7xkv8BPPe_qg</recordid><startdate>199606</startdate><enddate>199606</enddate><creator>Morga, Eleonora</creator><creator>Heuschling, Paul</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199606</creationdate><title>Interleukin-4 down-regulates MHC class II antigens on cultured rat astrocytes</title><author>Morga, Eleonora ; Heuschling, Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4619-f3051d6342e13fb36076705df4ca88f58da8752d6a63315a07e4ef74119d274f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Astrocytes - metabolism</topic><topic>Biological and medical sciences</topic><topic>cAMP</topic><topic>Cells, Cultured - metabolism</topic><topic>cGMP</topic><topic>Down-Regulation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gamma-interferon</topic><topic>Histocompatibility Antigens Class II - metabolism</topic><topic>Interleukin-4 - metabolism</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>major histocompatibility complex</topic><topic>nitric oxide</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Time Factors</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morga, Eleonora</creatorcontrib><creatorcontrib>Heuschling, Paul</creatorcontrib><collection>Istex</collection><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>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morga, Eleonora</au><au>Heuschling, Paul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interleukin-4 down-regulates MHC class II antigens on cultured rat astrocytes</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>1996-06</date><risdate>1996</risdate><volume>17</volume><issue>2</issue><spage>175</spage><epage>179</epage><pages>175-179</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><coden>GLIAEJ</coden><abstract>Mammalian cerebral astrocytes can be brought to express major histocompatibility complex (MHC) class II molecules upon appropriate stimulation. It is well established that this expression is subject to modulation by several neurotransmitters and cytokines. We show that the low, basal expression of MHC class II antigens on cultured rat astrocytes is concentration‐dependently down‐regulated by low concentrations of interleukin‐4 (IL‐4), reaching maximal inhibition at 10 U/ml. The higher, γ‐IFN‐induced, expression of class II molecules is also decreased by increasing concentrations of IL‐4, significant effects being already observed at 5 U/ml. Since the cAMP as well as the nitric oxide dependent cGMP pathway have previously been shown to mediate an inhibition on astroglial MHC class II expression, we measured the intra‐cellular content of cyclic nucleotides after stimulation with IL‐4. No rise in cAMP or cGMP is detected. Similarly, IL‐4 does not affect the induced synthesis of nitric oxide radicals. Since MHC class II expression is a critical step in many regulatory processes of the cellular immune reaction, IL‐4, via its activity on astroglial cells, emerges as an important modulator of immunological activities in the central nervous system. © 1996 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>8776584</pmid><doi>10.1002/(SICI)1098-1136(199606)17:2&lt;175::AID-GLIA9&gt;3.0.CO;2-1</doi><tpages>5</tpages></addata></record>
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subjects Animals
Astrocytes - metabolism
Biological and medical sciences
cAMP
Cells, Cultured - metabolism
cGMP
Down-Regulation
Fundamental and applied biological sciences. Psychology
gamma-interferon
Histocompatibility Antigens Class II - metabolism
Interleukin-4 - metabolism
Isolated neuron and nerve. Neuroglia
major histocompatibility complex
nitric oxide
Rats
Rats, Wistar
Time Factors
Vertebrates: nervous system and sense organs
title Interleukin-4 down-regulates MHC class II antigens on cultured rat astrocytes
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