Organ-specific distribution of major histocompatibility antigens in rats
The present study systematically investigated the expression and distribution of the major histocompatibility complex (MHC) classes I and II in the rat. About 150 native tissue probes from eight adult Lewis rats were taken, representative for most organs, tissues, and the vascular system. MHC expres...
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description | The present study systematically investigated the expression and distribution of the major histocompatibility complex (MHC) classes I and II in the rat. About 150 native tissue probes from eight adult Lewis rats were taken, representative for most organs, tissues, and the vascular system. MHC expression was analyzed by two monoclonal antibodies (mAb) generated against the non-polymorphic determinants of rat MHC class I (Ox-18) and class II (Ox-6). Immunoreactivities were compared to those of different endothelial (HIS52, TLD-3A12, Ox-43, REHA-1 antigen), histiocytic (ED1, ED2), B-cell (RLN-9D3), and T-cell (MRC Ox-52) markers. A nonspecific mAb (MR12/53) served as a negative control. Pretested concentrations on various tissues and the alkaline phosphatase-anti-alkaline phosphatase technique allowed semiquantitative evaluation of serial cryostat tissue sections. MHC class I expression was detected on most immunocompetent cells. Endothelial cells were stained heterogeneously along the vascular system and the organ-specific microcirculation. Furthermore, some organs showed staining of parenchymal cells. MHC class II was found on all immunocompetent cells positive for the B-cell marker and about 15% of cells positive for the histiocytic markers. Besides the well-known expression of MHC class II in the outer zone of the renal proximal tubule, further organ-specific cell forms were found positive. In conclusion, the present study outlines tissue-specific distribution of MHC I/ II and implies that each organ carries a variable immunologic burden that needs to be considered for any transplantation model. |
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About 150 native tissue probes from eight adult Lewis rats were taken, representative for most organs, tissues, and the vascular system. MHC expression was analyzed by two monoclonal antibodies (mAb) generated against the non-polymorphic determinants of rat MHC class I (Ox-18) and class II (Ox-6). Immunoreactivities were compared to those of different endothelial (HIS52, TLD-3A12, Ox-43, REHA-1 antigen), histiocytic (ED1, ED2), B-cell (RLN-9D3), and T-cell (MRC Ox-52) markers. A nonspecific mAb (MR12/53) served as a negative control. Pretested concentrations on various tissues and the alkaline phosphatase-anti-alkaline phosphatase technique allowed semiquantitative evaluation of serial cryostat tissue sections. MHC class I expression was detected on most immunocompetent cells. Endothelial cells were stained heterogeneously along the vascular system and the organ-specific microcirculation. Furthermore, some organs showed staining of parenchymal cells. MHC class II was found on all immunocompetent cells positive for the B-cell marker and about 15% of cells positive for the histiocytic markers. Besides the well-known expression of MHC class II in the outer zone of the renal proximal tubule, further organ-specific cell forms were found positive. In conclusion, the present study outlines tissue-specific distribution of MHC I/ II and implies that each organ carries a variable immunologic burden that needs to be considered for any transplantation model.</description><identifier>ISSN: 0179-0358</identifier><identifier>EISSN: 1437-9813</identifier><identifier>DOI: 10.1007/s003830050746</identifier><identifier>PMID: 10898231</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Adrenal Cortex - metabolism ; Adrenal Cortex - pathology ; Adrenal Medulla - metabolism ; Adrenal Medulla - pathology ; Animals ; Antibodies, Monoclonal ; Histocompatibility Antigens Class I - metabolism ; Histocompatibility Antigens Class II - metabolism ; Immunoenzyme Techniques ; Islets of Langerhans - metabolism ; Islets of Langerhans - pathology ; Male ; Rats ; Rats, Inbred Lew ; Thyroid Gland - metabolism ; Thyroid Gland - pathology ; Tissue Distribution</subject><ispartof>Pediatric surgery international, 2000-05, Vol.16 (4), p.285-292</ispartof><rights>Springer-Verlag Berlin Heidelberg 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-5febac624213cd870d93ca62dd996f8a2a07cc08098058ec31eb8cca64d8286c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10898231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Metzger, R</creatorcontrib><creatorcontrib>Mempel, T</creatorcontrib><creatorcontrib>Joppich, I</creatorcontrib><creatorcontrib>Till, H</creatorcontrib><title>Organ-specific distribution of major histocompatibility antigens in rats</title><title>Pediatric surgery international</title><addtitle>Pediatr Surg Int</addtitle><description>The present study systematically investigated the expression and distribution of the major histocompatibility complex (MHC) classes I and II in the rat. About 150 native tissue probes from eight adult Lewis rats were taken, representative for most organs, tissues, and the vascular system. MHC expression was analyzed by two monoclonal antibodies (mAb) generated against the non-polymorphic determinants of rat MHC class I (Ox-18) and class II (Ox-6). Immunoreactivities were compared to those of different endothelial (HIS52, TLD-3A12, Ox-43, REHA-1 antigen), histiocytic (ED1, ED2), B-cell (RLN-9D3), and T-cell (MRC Ox-52) markers. A nonspecific mAb (MR12/53) served as a negative control. Pretested concentrations on various tissues and the alkaline phosphatase-anti-alkaline phosphatase technique allowed semiquantitative evaluation of serial cryostat tissue sections. MHC class I expression was detected on most immunocompetent cells. Endothelial cells were stained heterogeneously along the vascular system and the organ-specific microcirculation. Furthermore, some organs showed staining of parenchymal cells. MHC class II was found on all immunocompetent cells positive for the B-cell marker and about 15% of cells positive for the histiocytic markers. Besides the well-known expression of MHC class II in the outer zone of the renal proximal tubule, further organ-specific cell forms were found positive. In conclusion, the present study outlines tissue-specific distribution of MHC I/ II and implies that each organ carries a variable immunologic burden that needs to be considered for any transplantation model.</description><subject>Adrenal Cortex - metabolism</subject><subject>Adrenal Cortex - pathology</subject><subject>Adrenal Medulla - metabolism</subject><subject>Adrenal Medulla - pathology</subject><subject>Animals</subject><subject>Antibodies, Monoclonal</subject><subject>Histocompatibility Antigens Class I - metabolism</subject><subject>Histocompatibility Antigens Class II - metabolism</subject><subject>Immunoenzyme Techniques</subject><subject>Islets of Langerhans - metabolism</subject><subject>Islets of Langerhans - pathology</subject><subject>Male</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>Thyroid Gland - metabolism</subject><subject>Thyroid Gland - pathology</subject><subject>Tissue Distribution</subject><issn>0179-0358</issn><issn>1437-9813</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpd0MFLwzAUBvAgipvTo1cpHrxVX5K2eTnKmE4Y7KLnkqbpzGibmqSH_fdWtoN6evD48fHxEXJL4ZECiKcAwJED5CCy4ozMacZFKpHyczIHKmQKPMcZuQphDwDIC3lJZhRQIuN0TtZbv1N9GgajbWN1UtsQva3GaF2fuCbp1N755HP6Ou26QUVb2dbGQ6L6aHemD4ntE69iuCYXjWqDuTndBfl4Wb0v1-lm-_q2fN6kOqM0pnljKqULljHKdY0Casm1KlhdS1k0qJgCoTUgSIQcjebUVKgnkdXIsNB8QR6OuYN3X6MJsexs0KZtVW_cGEpBGc8kkxO8_wf3bvT91K1kjAmWI4oJpUekvQvBm6YcvO2UP5QUyp99yz_7Tv7uFDpWnal_6eOg_Bsiv3V5</recordid><startdate>20000501</startdate><enddate>20000501</enddate><creator>Metzger, R</creator><creator>Mempel, T</creator><creator>Joppich, I</creator><creator>Till, H</creator><general>Springer Nature B.V</general><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20000501</creationdate><title>Organ-specific distribution of major histocompatibility antigens in rats</title><author>Metzger, R ; Mempel, T ; Joppich, I ; Till, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-5febac624213cd870d93ca62dd996f8a2a07cc08098058ec31eb8cca64d8286c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adrenal Cortex - metabolism</topic><topic>Adrenal Cortex - pathology</topic><topic>Adrenal Medulla - metabolism</topic><topic>Adrenal Medulla - pathology</topic><topic>Animals</topic><topic>Antibodies, Monoclonal</topic><topic>Histocompatibility Antigens Class I - metabolism</topic><topic>Histocompatibility Antigens Class II - metabolism</topic><topic>Immunoenzyme Techniques</topic><topic>Islets of Langerhans - metabolism</topic><topic>Islets of Langerhans - pathology</topic><topic>Male</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>Thyroid Gland - metabolism</topic><topic>Thyroid Gland - pathology</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Metzger, R</creatorcontrib><creatorcontrib>Mempel, T</creatorcontrib><creatorcontrib>Joppich, I</creatorcontrib><creatorcontrib>Till, H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric surgery international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Metzger, R</au><au>Mempel, T</au><au>Joppich, I</au><au>Till, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Organ-specific distribution of major histocompatibility antigens in rats</atitle><jtitle>Pediatric surgery international</jtitle><addtitle>Pediatr Surg Int</addtitle><date>2000-05-01</date><risdate>2000</risdate><volume>16</volume><issue>4</issue><spage>285</spage><epage>292</epage><pages>285-292</pages><issn>0179-0358</issn><eissn>1437-9813</eissn><abstract>The present study systematically investigated the expression and distribution of the major histocompatibility complex (MHC) classes I and II in the rat. About 150 native tissue probes from eight adult Lewis rats were taken, representative for most organs, tissues, and the vascular system. MHC expression was analyzed by two monoclonal antibodies (mAb) generated against the non-polymorphic determinants of rat MHC class I (Ox-18) and class II (Ox-6). Immunoreactivities were compared to those of different endothelial (HIS52, TLD-3A12, Ox-43, REHA-1 antigen), histiocytic (ED1, ED2), B-cell (RLN-9D3), and T-cell (MRC Ox-52) markers. A nonspecific mAb (MR12/53) served as a negative control. Pretested concentrations on various tissues and the alkaline phosphatase-anti-alkaline phosphatase technique allowed semiquantitative evaluation of serial cryostat tissue sections. MHC class I expression was detected on most immunocompetent cells. Endothelial cells were stained heterogeneously along the vascular system and the organ-specific microcirculation. Furthermore, some organs showed staining of parenchymal cells. MHC class II was found on all immunocompetent cells positive for the B-cell marker and about 15% of cells positive for the histiocytic markers. Besides the well-known expression of MHC class II in the outer zone of the renal proximal tubule, further organ-specific cell forms were found positive. In conclusion, the present study outlines tissue-specific distribution of MHC I/ II and implies that each organ carries a variable immunologic burden that needs to be considered for any transplantation model.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>10898231</pmid><doi>10.1007/s003830050746</doi><tpages>8</tpages></addata></record> |
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subjects | Adrenal Cortex - metabolism Adrenal Cortex - pathology Adrenal Medulla - metabolism Adrenal Medulla - pathology Animals Antibodies, Monoclonal Histocompatibility Antigens Class I - metabolism Histocompatibility Antigens Class II - metabolism Immunoenzyme Techniques Islets of Langerhans - metabolism Islets of Langerhans - pathology Male Rats Rats, Inbred Lew Thyroid Gland - metabolism Thyroid Gland - pathology Tissue Distribution |
title | Organ-specific distribution of major histocompatibility antigens in rats |
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