Contrasting effects of thymopentin and splenopentin on the capacity of female mice to reject syngeneic male skin
The TP-5 pentapeptide analog of thymopoietin and the SP-5 pentapeptide analog of splenin, which differ only in substitution of Glu for Asp and represent positions 32-36 of the parent molecules, were compared for effects on the capacity of C3H/HeJ female mice to reject C3H/HeJ male skin (the H-Y reje...
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Veröffentlicht in: | Transplantation 1984-07, Vol.38 (1), p.52-55 |
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description | The TP-5 pentapeptide analog of thymopoietin and the SP-5 pentapeptide analog of splenin, which differ only in substitution of Glu for Asp and represent positions 32-36 of the parent molecules, were compared for effects on the capacity of C3H/HeJ female mice to reject C3H/HeJ male skin (the H-Y rejection response). The actions of these TP-5 and SP-5 analogs of respective thymic and splenic products were already known to differ in other functional systems, neuromuscular and immunological, in vitro and in vivo. The H-Y rejection response of young thymus-intact female mice was heightened by TP-5 and by SP-5. Neither TP-5 nor SP-5 affected the raised H-Y rejection response of splenectomized female mice. Whereas TP-5 lowered the raised H-Y rejection response of thymectomized female mice, as reported elsewhere, SP-5 did not. Thus, not only do these structurally very similar immunoregulators differ in their particular functions, but the overall effect of these functions in vivo depends on the immune status of the recipient. |
doi_str_mv | 10.1097/00007890-198407000-00013 |
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H ; GOLDSTEIN, G ; HARMAN, D. B ; BOYSE, E. A</creator><creatorcontrib>GOLDBERG, E. H ; GOLDSTEIN, G ; HARMAN, D. B ; BOYSE, E. A</creatorcontrib><description>The TP-5 pentapeptide analog of thymopoietin and the SP-5 pentapeptide analog of splenin, which differ only in substitution of Glu for Asp and represent positions 32-36 of the parent molecules, were compared for effects on the capacity of C3H/HeJ female mice to reject C3H/HeJ male skin (the H-Y rejection response). The actions of these TP-5 and SP-5 analogs of respective thymic and splenic products were already known to differ in other functional systems, neuromuscular and immunological, in vitro and in vivo. The H-Y rejection response of young thymus-intact female mice was heightened by TP-5 and by SP-5. Neither TP-5 nor SP-5 affected the raised H-Y rejection response of splenectomized female mice. Whereas TP-5 lowered the raised H-Y rejection response of thymectomized female mice, as reported elsewhere, SP-5 did not. Thus, not only do these structurally very similar immunoregulators differ in their particular functions, but the overall effect of these functions in vivo depends on the immune status of the recipient.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/00007890-198407000-00013</identifier><identifier>PMID: 6377611</identifier><identifier>CODEN: TRPLAU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott</publisher><subject>Animals ; Biological and medical sciences ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Graft Rejection - drug effects ; Male ; Mice ; Mice, Inbred C3H ; Peptide Fragments - pharmacology ; Sex Factors ; Skin Transplantation ; Splenectomy ; Thymectomy ; Thymopentin ; Thymopoietins - pharmacology ; Thymus Hormones - pharmacology ; Tissue, organ and graft immunology</subject><ispartof>Transplantation, 1984-07, Vol.38 (1), p.52-55</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-510c2cee8a1ebfeab54335fc414043b2d0c7769780909aa9f564a268baf52d7d3</citedby></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=9021452$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6377611$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GOLDBERG, E. H</creatorcontrib><creatorcontrib>GOLDSTEIN, G</creatorcontrib><creatorcontrib>HARMAN, D. B</creatorcontrib><creatorcontrib>BOYSE, E. A</creatorcontrib><title>Contrasting effects of thymopentin and splenopentin on the capacity of female mice to reject syngeneic male skin</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>The TP-5 pentapeptide analog of thymopoietin and the SP-5 pentapeptide analog of splenin, which differ only in substitution of Glu for Asp and represent positions 32-36 of the parent molecules, were compared for effects on the capacity of C3H/HeJ female mice to reject C3H/HeJ male skin (the H-Y rejection response). The actions of these TP-5 and SP-5 analogs of respective thymic and splenic products were already known to differ in other functional systems, neuromuscular and immunological, in vitro and in vivo. The H-Y rejection response of young thymus-intact female mice was heightened by TP-5 and by SP-5. Neither TP-5 nor SP-5 affected the raised H-Y rejection response of splenectomized female mice. Whereas TP-5 lowered the raised H-Y rejection response of thymectomized female mice, as reported elsewhere, SP-5 did not. Thus, not only do these structurally very similar immunoregulators differ in their particular functions, but the overall effect of these functions in vivo depends on the immune status of the recipient.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Graft Rejection - drug effects</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Peptide Fragments - pharmacology</subject><subject>Sex Factors</subject><subject>Skin Transplantation</subject><subject>Splenectomy</subject><subject>Thymectomy</subject><subject>Thymopentin</subject><subject>Thymopoietins - pharmacology</subject><subject>Thymus Hormones - pharmacology</subject><subject>Tissue, organ and graft immunology</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1PwzAMhiMEgjH4CUg5IG6FuEna5IgmviQkLnCu3NSBQpuWpjvs35PBmCXLst_HjvIyxkFcg7DljUhRGisysEaJMnVZSpAHbAFaqqwQRhyyhRAKMpCyPGGnMX4mRMuyPGbHRSoFwIKNqyHME8a5De-cvCc3Rz54Pn9s-mGkkOYcQ8Pj2FH4Hwwh6cQdjujaebPlPfXYEe9bR3we-ESf6RKPm_BOgVrHf9X41YYzduSxi3S-q0v2dn_3unrMnl8enla3z5mTxs6ZBuFyR2QQqPaEtVZSau8UKKFknTfCpR_Y0ggrLKL1ulCYF6ZGr_OmbOSSXf3dHafhe01xrvo2Ouo6DDSsY2UANIDUCTR_oJuGGCfy1Ti1PU6bCkS1Nbv6N7vam139mp1WL3ZvrOuemv3izt2kX-50jA47P2FwbdxjVuSgdC5_AAqviFc</recordid><startdate>198407</startdate><enddate>198407</enddate><creator>GOLDBERG, E. H</creator><creator>GOLDSTEIN, G</creator><creator>HARMAN, D. B</creator><creator>BOYSE, E. A</creator><general>Lippincott</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>198407</creationdate><title>Contrasting effects of thymopentin and splenopentin on the capacity of female mice to reject syngeneic male skin</title><author>GOLDBERG, E. H ; GOLDSTEIN, G ; HARMAN, D. B ; BOYSE, E. A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-510c2cee8a1ebfeab54335fc414043b2d0c7769780909aa9f564a268baf52d7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Graft Rejection - drug effects</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Peptide Fragments - pharmacology</topic><topic>Sex Factors</topic><topic>Skin Transplantation</topic><topic>Splenectomy</topic><topic>Thymectomy</topic><topic>Thymopentin</topic><topic>Thymopoietins - pharmacology</topic><topic>Thymus Hormones - pharmacology</topic><topic>Tissue, organ and graft immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GOLDBERG, E. H</creatorcontrib><creatorcontrib>GOLDSTEIN, G</creatorcontrib><creatorcontrib>HARMAN, D. B</creatorcontrib><creatorcontrib>BOYSE, E. 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A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Contrasting effects of thymopentin and splenopentin on the capacity of female mice to reject syngeneic male skin</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>1984-07</date><risdate>1984</risdate><volume>38</volume><issue>1</issue><spage>52</spage><epage>55</epage><pages>52-55</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><coden>TRPLAU</coden><abstract>The TP-5 pentapeptide analog of thymopoietin and the SP-5 pentapeptide analog of splenin, which differ only in substitution of Glu for Asp and represent positions 32-36 of the parent molecules, were compared for effects on the capacity of C3H/HeJ female mice to reject C3H/HeJ male skin (the H-Y rejection response). The actions of these TP-5 and SP-5 analogs of respective thymic and splenic products were already known to differ in other functional systems, neuromuscular and immunological, in vitro and in vivo. The H-Y rejection response of young thymus-intact female mice was heightened by TP-5 and by SP-5. Neither TP-5 nor SP-5 affected the raised H-Y rejection response of splenectomized female mice. Whereas TP-5 lowered the raised H-Y rejection response of thymectomized female mice, as reported elsewhere, SP-5 did not. Thus, not only do these structurally very similar immunoregulators differ in their particular functions, but the overall effect of these functions in vivo depends on the immune status of the recipient.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>6377611</pmid><doi>10.1097/00007890-198407000-00013</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Female Fundamental and applied biological sciences. Psychology Fundamental immunology Graft Rejection - drug effects Male Mice Mice, Inbred C3H Peptide Fragments - pharmacology Sex Factors Skin Transplantation Splenectomy Thymectomy Thymopentin Thymopoietins - pharmacology Thymus Hormones - pharmacology Tissue, organ and graft immunology |
title | Contrasting effects of thymopentin and splenopentin on the capacity of female mice to reject syngeneic male skin |
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