Expression of NHERF-1, NHERF-2, PDGFR-α, and PDGFR-β in Normal Human Kidneys and in Renal Transplant Rejection
Sodium-hydrogen exchanger regulatory factor-1 and -2 (NHERF-1 and NHERF-2) are adaptor proteins that regulate renal electrolyte transport and interact with the platelet-derived growth factor receptors (PDGFR). The distribution of the NHERF proteins and PDGFR was studied in normal human kidneys and i...
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Veröffentlicht in: | Pathobiology (Basel) 2002-01, Vol.70 (6), p.314-323 |
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creator | Weinman, Edward J. Lakkis, Jay Akom, Michael Wali, Ravinder K. Drachenberg, Cinthia B. Coleman, Richard A. Wade, James B. |
description | Sodium-hydrogen exchanger regulatory factor-1 and -2 (NHERF-1 and NHERF-2) are adaptor proteins that regulate renal electrolyte transport and interact with the platelet-derived growth factor receptors (PDGFR). The distribution of the NHERF proteins and PDGFR was studied in normal human kidneys and in renal transplant rejection using immunocytochemistry. In normal kidneys, NHERF-1 was detected in proximal tubules. NHERF-2 was detected in glomeruli, peritubular capillaries, and collecting duct principal cells. NHERF-2 was also weakly detected in the proximal tubule. PDGFR-β was detected in glomeruli but not in tubules while PDGFR-α was detected in renal tubules and minimally in glomeruli. Acute and chronic transplant rejection was associated with increased expression of PDGFR-α in tubules and expression in the glomeruli. PDGFR-β expression in the glomeruli was increased in transplant rejection and became detectable in tubules. Expression of NHERF-1 and NHERF-2 was not different in the patient groups. These results indicate that in contrast to the rat, both NHERF isoforms are detected in the human proximal tubule. In renal transplant rejection, there is increased expression of both PDGFR subtypes consistent with a role for PDGF in injury or repair. |
doi_str_mv | 10.1159/000071271 |
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The distribution of the NHERF proteins and PDGFR was studied in normal human kidneys and in renal transplant rejection using immunocytochemistry. In normal kidneys, NHERF-1 was detected in proximal tubules. NHERF-2 was detected in glomeruli, peritubular capillaries, and collecting duct principal cells. NHERF-2 was also weakly detected in the proximal tubule. PDGFR-β was detected in glomeruli but not in tubules while PDGFR-α was detected in renal tubules and minimally in glomeruli. Acute and chronic transplant rejection was associated with increased expression of PDGFR-α in tubules and expression in the glomeruli. PDGFR-β expression in the glomeruli was increased in transplant rejection and became detectable in tubules. Expression of NHERF-1 and NHERF-2 was not different in the patient groups. These results indicate that in contrast to the rat, both NHERF isoforms are detected in the human proximal tubule. In renal transplant rejection, there is increased expression of both PDGFR subtypes consistent with a role for PDGF in injury or repair.</description><identifier>ISSN: 1015-2008</identifier><identifier>EISSN: 1423-0291</identifier><identifier>DOI: 10.1159/000071271</identifier><identifier>PMID: 12865627</identifier><language>eng</language><publisher>Basel, Switzerland</publisher><subject>Acute Disease ; Chronic Disease ; Cytoskeletal Proteins - metabolism ; Fluorescent Antibody Technique, Indirect ; Graft Rejection - immunology ; Graft Rejection - metabolism ; Graft Rejection - pathology ; Humans ; Kidney - metabolism ; Kidney Glomerulus - metabolism ; Kidney Glomerulus - pathology ; Kidney Transplantation - immunology ; Kidney Transplantation - pathology ; Kidney Tubules, Proximal - metabolism ; Kidney Tubules, Proximal - pathology ; Original Paper ; Phosphoproteins - metabolism ; Receptors, Platelet-Derived Growth Factor - metabolism ; Sodium-Hydrogen Exchangers</subject><ispartof>Pathobiology (Basel), 2002-01, Vol.70 (6), p.314-323</ispartof><rights>2003 S. Karger AG, Basel</rights><rights>Copyright 2003 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c301t-4654a454c4c21c55f9792ee43c295e01317aa2883bb2a27f6fc6b2874b94894d3</citedby><cites>FETCH-LOGICAL-c301t-4654a454c4c21c55f9792ee43c295e01317aa2883bb2a27f6fc6b2874b94894d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2429,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12865627$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weinman, Edward J.</creatorcontrib><creatorcontrib>Lakkis, Jay</creatorcontrib><creatorcontrib>Akom, Michael</creatorcontrib><creatorcontrib>Wali, Ravinder K.</creatorcontrib><creatorcontrib>Drachenberg, Cinthia B.</creatorcontrib><creatorcontrib>Coleman, Richard A.</creatorcontrib><creatorcontrib>Wade, James B.</creatorcontrib><title>Expression of NHERF-1, NHERF-2, PDGFR-α, and PDGFR-β in Normal Human Kidneys and in Renal Transplant Rejection</title><title>Pathobiology (Basel)</title><addtitle>Pathobiology</addtitle><description>Sodium-hydrogen exchanger regulatory factor-1 and -2 (NHERF-1 and NHERF-2) are adaptor proteins that regulate renal electrolyte transport and interact with the platelet-derived growth factor receptors (PDGFR). The distribution of the NHERF proteins and PDGFR was studied in normal human kidneys and in renal transplant rejection using immunocytochemistry. In normal kidneys, NHERF-1 was detected in proximal tubules. NHERF-2 was detected in glomeruli, peritubular capillaries, and collecting duct principal cells. NHERF-2 was also weakly detected in the proximal tubule. PDGFR-β was detected in glomeruli but not in tubules while PDGFR-α was detected in renal tubules and minimally in glomeruli. Acute and chronic transplant rejection was associated with increased expression of PDGFR-α in tubules and expression in the glomeruli. PDGFR-β expression in the glomeruli was increased in transplant rejection and became detectable in tubules. Expression of NHERF-1 and NHERF-2 was not different in the patient groups. These results indicate that in contrast to the rat, both NHERF isoforms are detected in the human proximal tubule. In renal transplant rejection, there is increased expression of both PDGFR subtypes consistent with a role for PDGF in injury or repair.</description><subject>Acute Disease</subject><subject>Chronic Disease</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Graft Rejection - immunology</subject><subject>Graft Rejection - metabolism</subject><subject>Graft Rejection - pathology</subject><subject>Humans</subject><subject>Kidney - metabolism</subject><subject>Kidney Glomerulus - metabolism</subject><subject>Kidney Glomerulus - pathology</subject><subject>Kidney Transplantation - immunology</subject><subject>Kidney Transplantation - pathology</subject><subject>Kidney Tubules, Proximal - metabolism</subject><subject>Kidney Tubules, Proximal - pathology</subject><subject>Original Paper</subject><subject>Phosphoproteins - metabolism</subject><subject>Receptors, Platelet-Derived Growth Factor - metabolism</subject><subject>Sodium-Hydrogen Exchangers</subject><issn>1015-2008</issn><issn>1423-0291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkFtLwzAUx4Mobk4ffBakT4KwapKmTfIocxdRpoz5XNI0lc42rUkL7mPpB_EzGW2d5-XcfufCH4BTBK8QCvk1dEYRpmgPDBHBgQ8xR_suhij0MYRsAI6s3TiKwQgeggHCLAojTIegnr7XRlmbV9qrMm-5mK5mPhr3AR57T7fz2cr_-hh7Qqd_2aeXa29ZmVIU3qIthfbu81Srrf2FXG-ltGutjdC2LoRuXGGjZOOuHIODTBRWnfR-BJ5n0_Vk4T88zu8mNw--DCBqfBKFRJCQSCIxkmGYccqxUiSQmIcKogBRITBjQZJggWkWZTJKMKMk4YRxkgYjcNHtrU311irbxGVupSrcN6pqbUwx4xGjzIGXHShNZa1RWVybvBRmGyMY_8gb7-R17Hm_tE1Klf6TvZ4OOOuAV2FelNkB3fg3yf96dw</recordid><startdate>20020101</startdate><enddate>20020101</enddate><creator>Weinman, Edward J.</creator><creator>Lakkis, Jay</creator><creator>Akom, Michael</creator><creator>Wali, Ravinder K.</creator><creator>Drachenberg, Cinthia B.</creator><creator>Coleman, Richard A.</creator><creator>Wade, James B.</creator><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>20020101</creationdate><title>Expression of NHERF-1, NHERF-2, PDGFR-α, and PDGFR-β in Normal Human Kidneys and in Renal Transplant Rejection</title><author>Weinman, Edward J. ; Lakkis, Jay ; Akom, Michael ; Wali, Ravinder K. ; Drachenberg, Cinthia B. ; Coleman, Richard A. ; Wade, James B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-4654a454c4c21c55f9792ee43c295e01317aa2883bb2a27f6fc6b2874b94894d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Acute Disease</topic><topic>Chronic Disease</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Graft Rejection - immunology</topic><topic>Graft Rejection - metabolism</topic><topic>Graft Rejection - pathology</topic><topic>Humans</topic><topic>Kidney - metabolism</topic><topic>Kidney Glomerulus - metabolism</topic><topic>Kidney Glomerulus - pathology</topic><topic>Kidney Transplantation - immunology</topic><topic>Kidney Transplantation - pathology</topic><topic>Kidney Tubules, Proximal - metabolism</topic><topic>Kidney Tubules, Proximal - pathology</topic><topic>Original Paper</topic><topic>Phosphoproteins - metabolism</topic><topic>Receptors, Platelet-Derived Growth Factor - metabolism</topic><topic>Sodium-Hydrogen Exchangers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weinman, Edward J.</creatorcontrib><creatorcontrib>Lakkis, Jay</creatorcontrib><creatorcontrib>Akom, Michael</creatorcontrib><creatorcontrib>Wali, Ravinder K.</creatorcontrib><creatorcontrib>Drachenberg, Cinthia B.</creatorcontrib><creatorcontrib>Coleman, Richard A.</creatorcontrib><creatorcontrib>Wade, James B.</creatorcontrib><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>Pathobiology (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weinman, Edward J.</au><au>Lakkis, Jay</au><au>Akom, Michael</au><au>Wali, Ravinder K.</au><au>Drachenberg, Cinthia B.</au><au>Coleman, Richard A.</au><au>Wade, James B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of NHERF-1, NHERF-2, PDGFR-α, and PDGFR-β in Normal Human Kidneys and in Renal Transplant Rejection</atitle><jtitle>Pathobiology (Basel)</jtitle><addtitle>Pathobiology</addtitle><date>2002-01-01</date><risdate>2002</risdate><volume>70</volume><issue>6</issue><spage>314</spage><epage>323</epage><pages>314-323</pages><issn>1015-2008</issn><eissn>1423-0291</eissn><abstract>Sodium-hydrogen exchanger regulatory factor-1 and -2 (NHERF-1 and NHERF-2) are adaptor proteins that regulate renal electrolyte transport and interact with the platelet-derived growth factor receptors (PDGFR). The distribution of the NHERF proteins and PDGFR was studied in normal human kidneys and in renal transplant rejection using immunocytochemistry. In normal kidneys, NHERF-1 was detected in proximal tubules. NHERF-2 was detected in glomeruli, peritubular capillaries, and collecting duct principal cells. NHERF-2 was also weakly detected in the proximal tubule. PDGFR-β was detected in glomeruli but not in tubules while PDGFR-α was detected in renal tubules and minimally in glomeruli. Acute and chronic transplant rejection was associated with increased expression of PDGFR-α in tubules and expression in the glomeruli. PDGFR-β expression in the glomeruli was increased in transplant rejection and became detectable in tubules. Expression of NHERF-1 and NHERF-2 was not different in the patient groups. These results indicate that in contrast to the rat, both NHERF isoforms are detected in the human proximal tubule. In renal transplant rejection, there is increased expression of both PDGFR subtypes consistent with a role for PDGF in injury or repair.</abstract><cop>Basel, Switzerland</cop><pmid>12865627</pmid><doi>10.1159/000071271</doi><tpages>10</tpages></addata></record> |
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subjects | Acute Disease Chronic Disease Cytoskeletal Proteins - metabolism Fluorescent Antibody Technique, Indirect Graft Rejection - immunology Graft Rejection - metabolism Graft Rejection - pathology Humans Kidney - metabolism Kidney Glomerulus - metabolism Kidney Glomerulus - pathology Kidney Transplantation - immunology Kidney Transplantation - pathology Kidney Tubules, Proximal - metabolism Kidney Tubules, Proximal - pathology Original Paper Phosphoproteins - metabolism Receptors, Platelet-Derived Growth Factor - metabolism Sodium-Hydrogen Exchangers |
title | Expression of NHERF-1, NHERF-2, PDGFR-α, and PDGFR-β in Normal Human Kidneys and in Renal Transplant Rejection |
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