Ureteric bud derivatives express angiotensinogen and AT1 receptors
1 Departments of Pediatrics 2 Physiology 3 Pathology, Tulane University School of Medicine, New Orleans, Louisiana 70112 Inactivation of the renin-angiotensin system interferes with the morphogenesis of the renal medulla. Thus ureteric bud (UB) derivatives may be a target for angiotensin production...
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creator | PRIETO, MINOLFA DIPP, SUSANA MELEG-SMITH, SUZANNE EL-DAHR, SAMIR S |
description | 1 Departments of Pediatrics
2 Physiology
3 Pathology, Tulane University School of Medicine, New Orleans, Louisiana 70112
Inactivation of the renin-angiotensin system interferes with the morphogenesis of the renal medulla. Thus ureteric bud (UB) derivatives may be a target for angiotensin production and action. To begin to test this hypothesis, we examined the cellular expression of angiotensinogen (Ao) and AT 1 receptor proteins during rat metanephrogenesis by immunohistochemistry. In addition, we tested whether UB-derived cells in culture express the Ao and AT 1 proteins. On embryonic day E15 , Ao and AT 1 are expressed in the UB branches and stromal mesenchyme. S-shaped bodies, including the vascular cleft, express AT 1 but not Ao. The metanephric mesenchyme and pretubular aggregates are Ao negative and AT 1 negative. Expression of Ao and AT 1 in UB branches and ampullae is also observed on E16 . However, UB expression of Ao is transient and is no longer detectable in the developing distal nephron beyond E17 . On E17 , both Ao and AT 1 are expressed in capillary loop glomeruli and proximal tubules, whereas UB branches express AT 1 only. By E18 , the majority of Ao immunoreactivity is clustered in terminally differentiated proximal tubules, whereas AT 1 receptors are expressed in both proximal and distal nephron segments. The specificity of Ao and AT 1 staining was documented by the elimination/attenuation of immunoreactivity after preadsorption of the primary antibodies with their respective antigens. Consistent with the in vivo findings, the AT 1 protein is abundantly expressed in cellular lysates of mouse UB ( E11.5 ) and IMCD3 (adult) cells. Moreover, AT 1 receptors in UB and IMCD3 cells are functional, since angiotensin II treatment elicits the tyrosine phosphorylation of the mitogen-activated protein kinases, ERK1/2. To our knowledge, this is the first demonstration of Ao and AT 1 protein expression in the developing distal nephron. Angiotensin II may have a paracrine role in the ontogeny of the collecting system.
nephrogenesis; renal medulla; collecting duct; proximal tubule; immunohistochemistry |
doi_str_mv | 10.1152/physiolgenomics.2001.6.1.29 |
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2 Physiology
3 Pathology, Tulane University School of Medicine, New Orleans, Louisiana 70112
Inactivation of the renin-angiotensin system interferes with the morphogenesis of the renal medulla. Thus ureteric bud (UB) derivatives may be a target for angiotensin production and action. To begin to test this hypothesis, we examined the cellular expression of angiotensinogen (Ao) and AT 1 receptor proteins during rat metanephrogenesis by immunohistochemistry. In addition, we tested whether UB-derived cells in culture express the Ao and AT 1 proteins. On embryonic day E15 , Ao and AT 1 are expressed in the UB branches and stromal mesenchyme. S-shaped bodies, including the vascular cleft, express AT 1 but not Ao. The metanephric mesenchyme and pretubular aggregates are Ao negative and AT 1 negative. Expression of Ao and AT 1 in UB branches and ampullae is also observed on E16 . However, UB expression of Ao is transient and is no longer detectable in the developing distal nephron beyond E17 . On E17 , both Ao and AT 1 are expressed in capillary loop glomeruli and proximal tubules, whereas UB branches express AT 1 only. By E18 , the majority of Ao immunoreactivity is clustered in terminally differentiated proximal tubules, whereas AT 1 receptors are expressed in both proximal and distal nephron segments. The specificity of Ao and AT 1 staining was documented by the elimination/attenuation of immunoreactivity after preadsorption of the primary antibodies with their respective antigens. Consistent with the in vivo findings, the AT 1 protein is abundantly expressed in cellular lysates of mouse UB ( E11.5 ) and IMCD3 (adult) cells. Moreover, AT 1 receptors in UB and IMCD3 cells are functional, since angiotensin II treatment elicits the tyrosine phosphorylation of the mitogen-activated protein kinases, ERK1/2. To our knowledge, this is the first demonstration of Ao and AT 1 protein expression in the developing distal nephron. Angiotensin II may have a paracrine role in the ontogeny of the collecting system.
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2 Physiology
3 Pathology, Tulane University School of Medicine, New Orleans, Louisiana 70112
Inactivation of the renin-angiotensin system interferes with the morphogenesis of the renal medulla. Thus ureteric bud (UB) derivatives may be a target for angiotensin production and action. To begin to test this hypothesis, we examined the cellular expression of angiotensinogen (Ao) and AT 1 receptor proteins during rat metanephrogenesis by immunohistochemistry. In addition, we tested whether UB-derived cells in culture express the Ao and AT 1 proteins. On embryonic day E15 , Ao and AT 1 are expressed in the UB branches and stromal mesenchyme. S-shaped bodies, including the vascular cleft, express AT 1 but not Ao. The metanephric mesenchyme and pretubular aggregates are Ao negative and AT 1 negative. Expression of Ao and AT 1 in UB branches and ampullae is also observed on E16 . However, UB expression of Ao is transient and is no longer detectable in the developing distal nephron beyond E17 . On E17 , both Ao and AT 1 are expressed in capillary loop glomeruli and proximal tubules, whereas UB branches express AT 1 only. By E18 , the majority of Ao immunoreactivity is clustered in terminally differentiated proximal tubules, whereas AT 1 receptors are expressed in both proximal and distal nephron segments. The specificity of Ao and AT 1 staining was documented by the elimination/attenuation of immunoreactivity after preadsorption of the primary antibodies with their respective antigens. Consistent with the in vivo findings, the AT 1 protein is abundantly expressed in cellular lysates of mouse UB ( E11.5 ) and IMCD3 (adult) cells. Moreover, AT 1 receptors in UB and IMCD3 cells are functional, since angiotensin II treatment elicits the tyrosine phosphorylation of the mitogen-activated protein kinases, ERK1/2. To our knowledge, this is the first demonstration of Ao and AT 1 protein expression in the developing distal nephron. Angiotensin II may have a paracrine role in the ontogeny of the collecting system.
nephrogenesis; renal medulla; collecting duct; proximal tubule; immunohistochemistry</description><subject>Angiotensinogen - immunology</subject><subject>Angiotensinogen - metabolism</subject><subject>Animals</subject><subject>Cell Line</subject><subject>Cells, Cultured</subject><subject>Epithelial Cells - metabolism</subject><subject>Immunohistochemistry</subject><subject>Kidney - embryology</subject><subject>Kidney - metabolism</subject><subject>Kidney Medulla - embryology</subject><subject>Kidney Tubules, Proximal - embryology</subject><subject>Kidney Tubules, Proximal - metabolism</subject><subject>Nephrons - cytology</subject><subject>Nephrons - embryology</subject><subject>Nephrons - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor, Angiotensin, Type 1</subject><subject>Receptor, Angiotensin, Type 2</subject><subject>Receptors, Angiotensin - immunology</subject><subject>Receptors, Angiotensin - metabolism</subject><subject>Ureter - embryology</subject><subject>Ureter - metabolism</subject><issn>1094-8341</issn><issn>1531-2267</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1Lw0AQhhdRbK3-BQkI3hJ3N7tJ9uChFqtCwUt7XvZj0q6kSdxNavvvDbReCp7mHXieGWYQeiA4IYTTp3ZzCK6p1lA3W2dCQjEmSZaQhIoLNCY8JTGlWX45ZCxYXKSMjNBNCF8Dx_KCX6MRIangnLExell56MA7E-neRnZIO9W5HYQI9q2HECJVr13TQR1c3Qw7h95G0yWJPBhou8aHW3RVqirA3alO0Gr-upy9x4vPt4_ZdBFvaJF1Mcc2N0ZbxmiBU65oqQnBCmtlC6UNY1kurC0sLTjhpgQjWKaFyRmlBmtt0gl6PM5tffPdQ-jk1gUDVaVqaPogcyxwIXI6gPcnsNdbsLL1bqv8Qf5dPQDPR2Dj1psf50GeftqsD3LeV9US9p08-3MmiaRCtrYcfPK_f6bJo5f-An_7ic8</recordid><startdate>20010606</startdate><enddate>20010606</enddate><creator>PRIETO, MINOLFA</creator><creator>DIPP, SUSANA</creator><creator>MELEG-SMITH, SUZANNE</creator><creator>EL-DAHR, SAMIR S</creator><general>Am Physiological Soc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20010606</creationdate><title>Ureteric bud derivatives express angiotensinogen and AT1 receptors</title><author>PRIETO, MINOLFA ; DIPP, SUSANA ; MELEG-SMITH, SUZANNE ; EL-DAHR, SAMIR S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h286t-50d7ccbd4428035a2fb110a0bad8abc44679dd8d28515cfec946b9c7422c0bbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Angiotensinogen - immunology</topic><topic>Angiotensinogen - metabolism</topic><topic>Animals</topic><topic>Cell Line</topic><topic>Cells, Cultured</topic><topic>Epithelial Cells - metabolism</topic><topic>Immunohistochemistry</topic><topic>Kidney - embryology</topic><topic>Kidney - metabolism</topic><topic>Kidney Medulla - embryology</topic><topic>Kidney Tubules, Proximal - embryology</topic><topic>Kidney Tubules, Proximal - metabolism</topic><topic>Nephrons - cytology</topic><topic>Nephrons - embryology</topic><topic>Nephrons - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor, Angiotensin, Type 1</topic><topic>Receptor, Angiotensin, Type 2</topic><topic>Receptors, Angiotensin - immunology</topic><topic>Receptors, Angiotensin - metabolism</topic><topic>Ureter - embryology</topic><topic>Ureter - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PRIETO, MINOLFA</creatorcontrib><creatorcontrib>DIPP, SUSANA</creatorcontrib><creatorcontrib>MELEG-SMITH, SUZANNE</creatorcontrib><creatorcontrib>EL-DAHR, SAMIR S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Physiological genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PRIETO, MINOLFA</au><au>DIPP, SUSANA</au><au>MELEG-SMITH, SUZANNE</au><au>EL-DAHR, SAMIR S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ureteric bud derivatives express angiotensinogen and AT1 receptors</atitle><jtitle>Physiological genomics</jtitle><addtitle>Physiol Genomics</addtitle><date>2001-06-06</date><risdate>2001</risdate><volume>6</volume><issue>1</issue><spage>29</spage><epage>37</epage><pages>29-37</pages><issn>1094-8341</issn><eissn>1531-2267</eissn><abstract>1 Departments of Pediatrics
2 Physiology
3 Pathology, Tulane University School of Medicine, New Orleans, Louisiana 70112
Inactivation of the renin-angiotensin system interferes with the morphogenesis of the renal medulla. Thus ureteric bud (UB) derivatives may be a target for angiotensin production and action. To begin to test this hypothesis, we examined the cellular expression of angiotensinogen (Ao) and AT 1 receptor proteins during rat metanephrogenesis by immunohistochemistry. In addition, we tested whether UB-derived cells in culture express the Ao and AT 1 proteins. On embryonic day E15 , Ao and AT 1 are expressed in the UB branches and stromal mesenchyme. S-shaped bodies, including the vascular cleft, express AT 1 but not Ao. The metanephric mesenchyme and pretubular aggregates are Ao negative and AT 1 negative. Expression of Ao and AT 1 in UB branches and ampullae is also observed on E16 . However, UB expression of Ao is transient and is no longer detectable in the developing distal nephron beyond E17 . On E17 , both Ao and AT 1 are expressed in capillary loop glomeruli and proximal tubules, whereas UB branches express AT 1 only. By E18 , the majority of Ao immunoreactivity is clustered in terminally differentiated proximal tubules, whereas AT 1 receptors are expressed in both proximal and distal nephron segments. The specificity of Ao and AT 1 staining was documented by the elimination/attenuation of immunoreactivity after preadsorption of the primary antibodies with their respective antigens. Consistent with the in vivo findings, the AT 1 protein is abundantly expressed in cellular lysates of mouse UB ( E11.5 ) and IMCD3 (adult) cells. Moreover, AT 1 receptors in UB and IMCD3 cells are functional, since angiotensin II treatment elicits the tyrosine phosphorylation of the mitogen-activated protein kinases, ERK1/2. To our knowledge, this is the first demonstration of Ao and AT 1 protein expression in the developing distal nephron. Angiotensin II may have a paracrine role in the ontogeny of the collecting system.
nephrogenesis; renal medulla; collecting duct; proximal tubule; immunohistochemistry</abstract><cop>United States</cop><pub>Am Physiological Soc</pub><pmid>11395544</pmid><doi>10.1152/physiolgenomics.2001.6.1.29</doi><tpages>9</tpages></addata></record> |
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subjects | Angiotensinogen - immunology Angiotensinogen - metabolism Animals Cell Line Cells, Cultured Epithelial Cells - metabolism Immunohistochemistry Kidney - embryology Kidney - metabolism Kidney Medulla - embryology Kidney Tubules, Proximal - embryology Kidney Tubules, Proximal - metabolism Nephrons - cytology Nephrons - embryology Nephrons - metabolism Rats Rats, Sprague-Dawley Receptor, Angiotensin, Type 1 Receptor, Angiotensin, Type 2 Receptors, Angiotensin - immunology Receptors, Angiotensin - metabolism Ureter - embryology Ureter - metabolism |
title | Ureteric bud derivatives express angiotensinogen and AT1 receptors |
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