Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patients
Rabbit antibody to human liver arginase was used to examine the immunologic characteristics of arginase in red blood cells (RBC), liver, kidney, brain, and gastrointestinal tract from normal adults and from patients with hyperargininemia. Greater than 90% of the arginase in RBC and liver was precipi...
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Veröffentlicht in: | Pediatric research 1983-12, Vol.17 (12), p.941-944 |
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description | Rabbit antibody to human liver arginase was used to examine the immunologic characteristics of arginase in red blood cells (RBC), liver, kidney, brain, and gastrointestinal tract from normal adults and from patients with hyperargininemia. Greater than 90% of the arginase in RBC and liver was precipitated by this antibody whereas only 50% of the arginase in kidney, brain, and gastrointestinal tract reacted with it. Two siblings and a third patient with hyperargininemia were found to have immunoreactive arginase protein in their RBC that was enzymatically inactive. The amount of arginase protein approximated that found in RBC from normal individuals. A kidney biopsy obtained from one of the patients with hyperargininemia had arginase activity 4-5-fold greater than that found in normal kidney biopsy material. Double immunodiffusion and precipitation-inhibition studies demonstrated two types of arginase protein in this patient's kidney: one enzymatically inactive and precipitated by the antibody, and one enzymatically active but not precipitated by the antibody. These data, in conjunction with biochemical data reported previously demonstrate that there are two gene loci determining arginase in man. |
doi_str_mv | 10.1203/00006450-198312000-00003 |
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B ; RICE, S. C. H ; CEDERBAUM, S. D</creator><creatorcontrib>SPECTOR, E. B ; RICE, S. C. H ; CEDERBAUM, S. D</creatorcontrib><description>Rabbit antibody to human liver arginase was used to examine the immunologic characteristics of arginase in red blood cells (RBC), liver, kidney, brain, and gastrointestinal tract from normal adults and from patients with hyperargininemia. Greater than 90% of the arginase in RBC and liver was precipitated by this antibody whereas only 50% of the arginase in kidney, brain, and gastrointestinal tract reacted with it. Two siblings and a third patient with hyperargininemia were found to have immunoreactive arginase protein in their RBC that was enzymatically inactive. The amount of arginase protein approximated that found in RBC from normal individuals. A kidney biopsy obtained from one of the patients with hyperargininemia had arginase activity 4-5-fold greater than that found in normal kidney biopsy material. Double immunodiffusion and precipitation-inhibition studies demonstrated two types of arginase protein in this patient's kidney: one enzymatically inactive and precipitated by the antibody, and one enzymatically active but not precipitated by the antibody. These data, in conjunction with biochemical data reported previously demonstrate that there are two gene loci determining arginase in man.</description><identifier>ISSN: 0031-3998</identifier><identifier>EISSN: 1530-0447</identifier><identifier>DOI: 10.1203/00006450-198312000-00003</identifier><identifier>PMID: 6419196</identifier><identifier>CODEN: PEREBL</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Amino Acid Metabolism, Inborn Errors - enzymology ; Amino Acid Metabolism, Inborn Errors - genetics ; Aminoacid disorders ; Arginase - genetics ; Arginase - immunology ; Arginine - blood ; Biological and medical sciences ; Brain - enzymology ; Chromosome Mapping ; Digestive System - enzymology ; Errors of metabolism ; Erythrocytes - enzymology ; Genes ; Humans ; Hyperargininemia ; Immunodiffusion ; Kidney - enzymology ; Medical sciences ; Metabolic diseases</subject><ispartof>Pediatric research, 1983-12, Vol.17 (12), p.941-944</ispartof><rights>1984 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3703-1532d50cf85eb30f826972c73c3699cd190ffd1b3f609df25a19737b3bbe9d823</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9628033$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6419196$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SPECTOR, E. B</creatorcontrib><creatorcontrib>RICE, S. C. H</creatorcontrib><creatorcontrib>CEDERBAUM, S. D</creatorcontrib><title>Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patients</title><title>Pediatric research</title><addtitle>Pediatr Res</addtitle><description>Rabbit antibody to human liver arginase was used to examine the immunologic characteristics of arginase in red blood cells (RBC), liver, kidney, brain, and gastrointestinal tract from normal adults and from patients with hyperargininemia. Greater than 90% of the arginase in RBC and liver was precipitated by this antibody whereas only 50% of the arginase in kidney, brain, and gastrointestinal tract reacted with it. Two siblings and a third patient with hyperargininemia were found to have immunoreactive arginase protein in their RBC that was enzymatically inactive. The amount of arginase protein approximated that found in RBC from normal individuals. A kidney biopsy obtained from one of the patients with hyperargininemia had arginase activity 4-5-fold greater than that found in normal kidney biopsy material. Double immunodiffusion and precipitation-inhibition studies demonstrated two types of arginase protein in this patient's kidney: one enzymatically inactive and precipitated by the antibody, and one enzymatically active but not precipitated by the antibody. These data, in conjunction with biochemical data reported previously demonstrate that there are two gene loci determining arginase in man.</description><subject>Amino Acid Metabolism, Inborn Errors - enzymology</subject><subject>Amino Acid Metabolism, Inborn Errors - genetics</subject><subject>Aminoacid disorders</subject><subject>Arginase - genetics</subject><subject>Arginase - immunology</subject><subject>Arginine - blood</subject><subject>Biological and medical sciences</subject><subject>Brain - enzymology</subject><subject>Chromosome Mapping</subject><subject>Digestive System - enzymology</subject><subject>Errors of metabolism</subject><subject>Erythrocytes - enzymology</subject><subject>Genes</subject><subject>Humans</subject><subject>Hyperargininemia</subject><subject>Immunodiffusion</subject><subject>Kidney - enzymology</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><issn>0031-3998</issn><issn>1530-0447</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMlOwzAQhi0EKqXwCEg-IG6BcSaLfUQVS6VKXOAcHC_FKHFKnBx4e1waMpfR_PPPoo8QyuCOpYD3EKPIckiY4BgVgOQg4QlZshxjkWXlKVlGhSUoBD8nFyF8AbAs59mCLIqMCSaKJfnYtO3ou6bbOUXDMGpnAu0slf3OeRkMdZ4OLoTxKPuub2VDP8dWeir12AxUej27E22sU874ge7lcMjhkpxZ2QRzNeUVeX96fFu_JNvX5836YZsoLAGT-HWqc1CW56ZGsDwtRJmqEhUWQijNBFirWY22AKFtmksmSixrrGsjNE9xRW6Pe_d99x2_HarWBWWaRnrTjaHiEEFlCNHIj0bVdyH0xlb73rWy_6kYVAe41T_caob7J2EcvZ5ujHVr9Dw40Yz9m6kvg5KN7aVXLsw2UaQ8bsFfrNWB4w</recordid><startdate>198312</startdate><enddate>198312</enddate><creator>SPECTOR, E. B</creator><creator>RICE, S. C. H</creator><creator>CEDERBAUM, S. D</creator><general>Lippincott Williams & Wilkins</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>198312</creationdate><title>Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patients</title><author>SPECTOR, E. B ; RICE, S. C. H ; CEDERBAUM, S. D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3703-1532d50cf85eb30f826972c73c3699cd190ffd1b3f609df25a19737b3bbe9d823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Amino Acid Metabolism, Inborn Errors - enzymology</topic><topic>Amino Acid Metabolism, Inborn Errors - genetics</topic><topic>Aminoacid disorders</topic><topic>Arginase - genetics</topic><topic>Arginase - immunology</topic><topic>Arginine - blood</topic><topic>Biological and medical sciences</topic><topic>Brain - enzymology</topic><topic>Chromosome Mapping</topic><topic>Digestive System - enzymology</topic><topic>Errors of metabolism</topic><topic>Erythrocytes - enzymology</topic><topic>Genes</topic><topic>Humans</topic><topic>Hyperargininemia</topic><topic>Immunodiffusion</topic><topic>Kidney - enzymology</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SPECTOR, E. B</creatorcontrib><creatorcontrib>RICE, S. C. H</creatorcontrib><creatorcontrib>CEDERBAUM, S. D</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>Pediatric research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SPECTOR, E. B</au><au>RICE, S. C. H</au><au>CEDERBAUM, S. D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patients</atitle><jtitle>Pediatric research</jtitle><addtitle>Pediatr Res</addtitle><date>1983-12</date><risdate>1983</risdate><volume>17</volume><issue>12</issue><spage>941</spage><epage>944</epage><pages>941-944</pages><issn>0031-3998</issn><eissn>1530-0447</eissn><coden>PEREBL</coden><abstract>Rabbit antibody to human liver arginase was used to examine the immunologic characteristics of arginase in red blood cells (RBC), liver, kidney, brain, and gastrointestinal tract from normal adults and from patients with hyperargininemia. Greater than 90% of the arginase in RBC and liver was precipitated by this antibody whereas only 50% of the arginase in kidney, brain, and gastrointestinal tract reacted with it. Two siblings and a third patient with hyperargininemia were found to have immunoreactive arginase protein in their RBC that was enzymatically inactive. The amount of arginase protein approximated that found in RBC from normal individuals. A kidney biopsy obtained from one of the patients with hyperargininemia had arginase activity 4-5-fold greater than that found in normal kidney biopsy material. Double immunodiffusion and precipitation-inhibition studies demonstrated two types of arginase protein in this patient's kidney: one enzymatically inactive and precipitated by the antibody, and one enzymatically active but not precipitated by the antibody. These data, in conjunction with biochemical data reported previously demonstrate that there are two gene loci determining arginase in man.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>6419196</pmid><doi>10.1203/00006450-198312000-00003</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Ovid Autoload; Alma/SFX Local Collection |
subjects | Amino Acid Metabolism, Inborn Errors - enzymology Amino Acid Metabolism, Inborn Errors - genetics Aminoacid disorders Arginase - genetics Arginase - immunology Arginine - blood Biological and medical sciences Brain - enzymology Chromosome Mapping Digestive System - enzymology Errors of metabolism Erythrocytes - enzymology Genes Humans Hyperargininemia Immunodiffusion Kidney - enzymology Medical sciences Metabolic diseases |
title | Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patients |
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