Expression of MT-3 protein in the human kidney
The objective of the present study was to determine the expression of MT-3 in the human kidney. To accomplish this, an antibody was generated against a unique 8 amino acid sequence present in MT-3 that is not shared by any other MT family member. Western analysis demonstrated that the resulting anti...
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Veröffentlicht in: | Toxicology letters 1999-04, Vol.105 (3), p.207-214 |
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description | The objective of the present study was to determine the expression of MT-3 in the human kidney. To accomplish this, an antibody was generated against a unique 8 amino acid sequence present in MT-3 that is not shared by any other MT family member. Western analysis demonstrated that the resulting antibody reacted with a protein band of approximately 6 kDa, corresponding to the known molecular weight of MT-3. Immunohistochemical staining using this antibody demonstrated reactivity with several epithelial components of the nephron. In the glomerulus, moderate intensity was demonstrated in parietal epithelial cells of Bowman’s capsule and in visceral epithelial cells of the glomerular tuft. Proximal convoluted tubule cells exhibited moderate cytoplasmic MT-3 reactivity. Distal tubules showed strong cytoplasmic staining for MT-3, particularly in the medullary rays. In the medulla, MT-3 staining was the most variable, with weak to moderate staining in the medullary collecting ducts and a general absence of staining in the thin loops of Henle and in the transitional epithelium of the renal pelvis. The finding that MT-3 is constitutively expressed in several glomerular and tubular epithelial elements of the human kidney warrants consideration of an expanded role for this protein family in maintaining renal homeostasis. |
doi_str_mv | 10.1016/S0378-4274(99)00003-X |
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To accomplish this, an antibody was generated against a unique 8 amino acid sequence present in MT-3 that is not shared by any other MT family member. Western analysis demonstrated that the resulting antibody reacted with a protein band of approximately 6 kDa, corresponding to the known molecular weight of MT-3. Immunohistochemical staining using this antibody demonstrated reactivity with several epithelial components of the nephron. In the glomerulus, moderate intensity was demonstrated in parietal epithelial cells of Bowman’s capsule and in visceral epithelial cells of the glomerular tuft. Proximal convoluted tubule cells exhibited moderate cytoplasmic MT-3 reactivity. Distal tubules showed strong cytoplasmic staining for MT-3, particularly in the medullary rays. In the medulla, MT-3 staining was the most variable, with weak to moderate staining in the medullary collecting ducts and a general absence of staining in the thin loops of Henle and in the transitional epithelium of the renal pelvis. The finding that MT-3 is constitutively expressed in several glomerular and tubular epithelial elements of the human kidney warrants consideration of an expanded role for this protein family in maintaining renal homeostasis.</description><identifier>ISSN: 0378-4274</identifier><identifier>EISSN: 1879-3169</identifier><identifier>DOI: 10.1016/S0378-4274(99)00003-X</identifier><identifier>PMID: 10355541</identifier><identifier>CODEN: TOLED5</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Biological and medical sciences ; Blotting, Western ; Brain - metabolism ; Chemical and industrial products toxicology. Toxic occupational diseases ; Humans ; Immunohistochemistry ; Kidney ; Kidney - metabolism ; Medical sciences ; Metallothionein ; Metallothionein - analysis ; Metallothionein - biosynthesis ; Metals ; Metals and various inorganic compounds ; MT-3 ; Nephrotoxicity ; Proximal tubule ; Toxicology</subject><ispartof>Toxicology letters, 1999-04, Vol.105 (3), p.207-214</ispartof><rights>1999 Elsevier Science Ireland Ltd</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-a124dc05be1a377c9fda551f5dc10f52997c60dcae113bce1d41fd1ba96a4f013</citedby><cites>FETCH-LOGICAL-c456t-a124dc05be1a377c9fda551f5dc10f52997c60dcae113bce1d41fd1ba96a4f013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S037842749900003X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1839790$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10355541$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garrett, Scott H.</creatorcontrib><creatorcontrib>Sens, Mary Ann</creatorcontrib><creatorcontrib>Todd, John H.</creatorcontrib><creatorcontrib>Somji, Seema</creatorcontrib><creatorcontrib>Sens, Donald A.</creatorcontrib><title>Expression of MT-3 protein in the human kidney</title><title>Toxicology letters</title><addtitle>Toxicol Lett</addtitle><description>The objective of the present study was to determine the expression of MT-3 in the human kidney. To accomplish this, an antibody was generated against a unique 8 amino acid sequence present in MT-3 that is not shared by any other MT family member. Western analysis demonstrated that the resulting antibody reacted with a protein band of approximately 6 kDa, corresponding to the known molecular weight of MT-3. Immunohistochemical staining using this antibody demonstrated reactivity with several epithelial components of the nephron. In the glomerulus, moderate intensity was demonstrated in parietal epithelial cells of Bowman’s capsule and in visceral epithelial cells of the glomerular tuft. Proximal convoluted tubule cells exhibited moderate cytoplasmic MT-3 reactivity. Distal tubules showed strong cytoplasmic staining for MT-3, particularly in the medullary rays. In the medulla, MT-3 staining was the most variable, with weak to moderate staining in the medullary collecting ducts and a general absence of staining in the thin loops of Henle and in the transitional epithelium of the renal pelvis. The finding that MT-3 is constitutively expressed in several glomerular and tubular epithelial elements of the human kidney warrants consideration of an expanded role for this protein family in maintaining renal homeostasis.</description><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Brain - metabolism</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Kidney</subject><subject>Kidney - metabolism</subject><subject>Medical sciences</subject><subject>Metallothionein</subject><subject>Metallothionein - analysis</subject><subject>Metallothionein - biosynthesis</subject><subject>Metals</subject><subject>Metals and various inorganic compounds</subject><subject>MT-3</subject><subject>Nephrotoxicity</subject><subject>Proximal tubule</subject><subject>Toxicology</subject><issn>0378-4274</issn><issn>1879-3169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEQhoMoWqs_QdmDiB62ZpqPbU4i4hdUPFiht5AmE4y2uzXZiv57U1vUm8PAXJ6ZeXkIOQDaAwry7JGyalDyfsVPlDqluVg53iAdGFSqZCDVJun8IDtkN6WXzEguxTbZAcqEEBw6pHf1MY-YUmjqovHF_ahkxTw2LYa6yN0-Y_G8mJm6eA2uxs89suXNNOH-enbJ0_XV6PK2HD7c3F1eDEvLhWxLA33uLBUTBMOqyirvjBDghbNAvegrVVlJnTUIwCYWwXHwDiZGScM9BdYlx6u7OcvbAlOrZyFZnE5Njc0iaakqxUHyDIoVaGOTUkSv5zHMTPzUQPVSlP4WpZcWtFL6W5Qe573D9YPFZIbuz9bKTAaO1oBJ1kx9NLUN6ZcbsByBZux8hWG28R4w6mQD1hZdiGhb7ZrwT5Iv8omDtQ</recordid><startdate>19990412</startdate><enddate>19990412</enddate><creator>Garrett, Scott H.</creator><creator>Sens, Mary Ann</creator><creator>Todd, John H.</creator><creator>Somji, Seema</creator><creator>Sens, Donald A.</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Science</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>19990412</creationdate><title>Expression of MT-3 protein in the human kidney</title><author>Garrett, Scott H. ; Sens, Mary Ann ; Todd, John H. ; Somji, Seema ; Sens, Donald A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-a124dc05be1a377c9fda551f5dc10f52997c60dcae113bce1d41fd1ba96a4f013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Brain - metabolism</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Kidney</topic><topic>Kidney - metabolism</topic><topic>Medical sciences</topic><topic>Metallothionein</topic><topic>Metallothionein - analysis</topic><topic>Metallothionein - biosynthesis</topic><topic>Metals</topic><topic>Metals and various inorganic compounds</topic><topic>MT-3</topic><topic>Nephrotoxicity</topic><topic>Proximal tubule</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garrett, Scott H.</creatorcontrib><creatorcontrib>Sens, Mary Ann</creatorcontrib><creatorcontrib>Todd, John H.</creatorcontrib><creatorcontrib>Somji, Seema</creatorcontrib><creatorcontrib>Sens, Donald A.</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>Toxicology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garrett, Scott H.</au><au>Sens, Mary Ann</au><au>Todd, John H.</au><au>Somji, Seema</au><au>Sens, Donald A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of MT-3 protein in the human kidney</atitle><jtitle>Toxicology letters</jtitle><addtitle>Toxicol Lett</addtitle><date>1999-04-12</date><risdate>1999</risdate><volume>105</volume><issue>3</issue><spage>207</spage><epage>214</epage><pages>207-214</pages><issn>0378-4274</issn><eissn>1879-3169</eissn><coden>TOLED5</coden><abstract>The objective of the present study was to determine the expression of MT-3 in the human kidney. To accomplish this, an antibody was generated against a unique 8 amino acid sequence present in MT-3 that is not shared by any other MT family member. Western analysis demonstrated that the resulting antibody reacted with a protein band of approximately 6 kDa, corresponding to the known molecular weight of MT-3. Immunohistochemical staining using this antibody demonstrated reactivity with several epithelial components of the nephron. In the glomerulus, moderate intensity was demonstrated in parietal epithelial cells of Bowman’s capsule and in visceral epithelial cells of the glomerular tuft. Proximal convoluted tubule cells exhibited moderate cytoplasmic MT-3 reactivity. Distal tubules showed strong cytoplasmic staining for MT-3, particularly in the medullary rays. In the medulla, MT-3 staining was the most variable, with weak to moderate staining in the medullary collecting ducts and a general absence of staining in the thin loops of Henle and in the transitional epithelium of the renal pelvis. The finding that MT-3 is constitutively expressed in several glomerular and tubular epithelial elements of the human kidney warrants consideration of an expanded role for this protein family in maintaining renal homeostasis.</abstract><cop>Shannon</cop><cop>Amsterdam</cop><pub>Elsevier Ireland Ltd</pub><pmid>10355541</pmid><doi>10.1016/S0378-4274(99)00003-X</doi><tpages>8</tpages></addata></record> |
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subjects | Biological and medical sciences Blotting, Western Brain - metabolism Chemical and industrial products toxicology. Toxic occupational diseases Humans Immunohistochemistry Kidney Kidney - metabolism Medical sciences Metallothionein Metallothionein - analysis Metallothionein - biosynthesis Metals Metals and various inorganic compounds MT-3 Nephrotoxicity Proximal tubule Toxicology |
title | Expression of MT-3 protein in the human kidney |
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