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Changes in cellular composition of kidney collecting duct cells in rats with lithium-induced NDI
1 Water and Salt Research Center, 2 Institute of Anatomy, and 4 Institute of Experimental Clinical Research, University of Aarhus, DK-8000 Denmark; and 3 School of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom Submitted 26 June 2003 ; accepted in final form 4 November 2003...
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Published in: | American Journal of Physiology: Cell Physiology 2004-04, Vol.286 (4), p.C952-C964 |
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container_end_page | C964 |
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container_title | American Journal of Physiology: Cell Physiology |
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creator | Christensen, Birgitte Monster Marples, David Kim, Young-Hee Wang, Weidong Frokiaer, Jorgen Nielsen, Soren |
description | 1 Water and Salt Research Center, 2 Institute of Anatomy, and 4 Institute of Experimental Clinical Research, University of Aarhus, DK-8000 Denmark; and 3 School of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom
Submitted 26 June 2003
; accepted in final form 4 November 2003
Lithium treatment for 4 wk caused severe polyuria, dramatic downregulation in aquaporin-2 (AQP-2) expression, and marked decrease in AQP-2 immunoreactivity with the appearance of a large number of cells without AQP-2 labeling in the collecting ducts after lithium treatment. Surprisingly, this was not all due to an increase in AQP-2-negative principal cells, because double immunolabeling revealed that the majority of the AQP-2-negative cells displayed [H + ]ATPase labeling, which identified them as intercalated cells. Moreover, multiple [H + ]ATPase-labeled cells were adjacent, which was never seen in control rats. Quantitation confirmed a significant decrease in the fraction of collecting duct cells that exhibited detectable AQP-2 labeling compared with control rats: in cortical collecting ducts, 40 ± 3.4 vs. 62 ± 1.8% of controls ( P < 0.05; n = 4) and in inner medullary collecting ducts, 58 ± 1.6 vs. 81 ± 1.3% of controls ( P < 0.05; n = 4). In parallel, a significant increase in the fraction of intercalated ([H + ]ATPase-positive) cells was shown. Urine output, whole kidney AQP-2 expression, cellular organization, and the fractions of principal and intercalated cells in cortex and inner medulla returned to control levels after 4 wk on a lithium-free diet following 4 wk on a lithium-containing diet. In conclusion, lithium treatment not only decreased AQP-2 expression, but dramatically and reversibly reduced the fraction of principal cells and altered the cellular organization in collecting ducts. These effects are likely to be important in lithium-induced nephrogenic diabetes insipidus.
nephrogenic diabetes insipidus; aquaporin; exchanger
Address for reprint requests and other correspondence: S. Nielsen, Water and Salt Research Center, Institute of Anatomy, Univ. of Aarhus, DK-8000 Aarhus, Denmark (E-mail: sn{at}ana.au.dk ). |
doi_str_mv | 10.1152/ajpcell.00266.2003 |
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Submitted 26 June 2003
; accepted in final form 4 November 2003
Lithium treatment for 4 wk caused severe polyuria, dramatic downregulation in aquaporin-2 (AQP-2) expression, and marked decrease in AQP-2 immunoreactivity with the appearance of a large number of cells without AQP-2 labeling in the collecting ducts after lithium treatment. Surprisingly, this was not all due to an increase in AQP-2-negative principal cells, because double immunolabeling revealed that the majority of the AQP-2-negative cells displayed [H + ]ATPase labeling, which identified them as intercalated cells. Moreover, multiple [H + ]ATPase-labeled cells were adjacent, which was never seen in control rats. Quantitation confirmed a significant decrease in the fraction of collecting duct cells that exhibited detectable AQP-2 labeling compared with control rats: in cortical collecting ducts, 40 ± 3.4 vs. 62 ± 1.8% of controls ( P < 0.05; n = 4) and in inner medullary collecting ducts, 58 ± 1.6 vs. 81 ± 1.3% of controls ( P < 0.05; n = 4). In parallel, a significant increase in the fraction of intercalated ([H + ]ATPase-positive) cells was shown. Urine output, whole kidney AQP-2 expression, cellular organization, and the fractions of principal and intercalated cells in cortex and inner medulla returned to control levels after 4 wk on a lithium-free diet following 4 wk on a lithium-containing diet. In conclusion, lithium treatment not only decreased AQP-2 expression, but dramatically and reversibly reduced the fraction of principal cells and altered the cellular organization in collecting ducts. These effects are likely to be important in lithium-induced nephrogenic diabetes insipidus.
nephrogenic diabetes insipidus; aquaporin; exchanger
Address for reprint requests and other correspondence: S. Nielsen, Water and Salt Research Center, Institute of Anatomy, Univ. of Aarhus, DK-8000 Aarhus, Denmark (E-mail: sn{at}ana.au.dk ).</description><identifier>ISSN: 0363-6143</identifier><identifier>EISSN: 1522-1563</identifier><identifier>DOI: 10.1152/ajpcell.00266.2003</identifier><identifier>PMID: 14613889</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Antibodies ; Aquaporin 2 ; Aquaporin 4 ; Aquaporin 6 ; Aquaporins - immunology ; Aquaporins - metabolism ; Carrier Proteins - immunology ; Carrier Proteins - metabolism ; Diabetes Insipidus, Nephrogenic - chemically induced ; Diabetes Insipidus, Nephrogenic - metabolism ; Down-Regulation - drug effects ; Kidney Tubules, Collecting - drug effects ; Kidney Tubules, Collecting - metabolism ; Kidney Tubules, Collecting - ultrastructure ; Lithium - pharmacology ; Membrane Transport Proteins ; Microscopy, Immunoelectron ; Proton-Translocating ATPases - immunology ; Proton-Translocating ATPases - metabolism ; Rats ; Rats, Wistar ; Recovery of Function ; Urine</subject><ispartof>American Journal of Physiology: Cell Physiology, 2004-04, Vol.286 (4), p.C952-C964</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-fc20f1762e387c3886b38e92ebdd482f188a9ffd34915d783a8d1ffa61dfe9533</citedby><cites>FETCH-LOGICAL-c387t-fc20f1762e387c3886b38e92ebdd482f188a9ffd34915d783a8d1ffa61dfe9533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14613889$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Christensen, Birgitte Monster</creatorcontrib><creatorcontrib>Marples, David</creatorcontrib><creatorcontrib>Kim, Young-Hee</creatorcontrib><creatorcontrib>Wang, Weidong</creatorcontrib><creatorcontrib>Frokiaer, Jorgen</creatorcontrib><creatorcontrib>Nielsen, Soren</creatorcontrib><title>Changes in cellular composition of kidney collecting duct cells in rats with lithium-induced NDI</title><title>American Journal of Physiology: Cell Physiology</title><addtitle>Am J Physiol Cell Physiol</addtitle><description>1 Water and Salt Research Center, 2 Institute of Anatomy, and 4 Institute of Experimental Clinical Research, University of Aarhus, DK-8000 Denmark; and 3 School of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom
Submitted 26 June 2003
; accepted in final form 4 November 2003
Lithium treatment for 4 wk caused severe polyuria, dramatic downregulation in aquaporin-2 (AQP-2) expression, and marked decrease in AQP-2 immunoreactivity with the appearance of a large number of cells without AQP-2 labeling in the collecting ducts after lithium treatment. Surprisingly, this was not all due to an increase in AQP-2-negative principal cells, because double immunolabeling revealed that the majority of the AQP-2-negative cells displayed [H + ]ATPase labeling, which identified them as intercalated cells. Moreover, multiple [H + ]ATPase-labeled cells were adjacent, which was never seen in control rats. Quantitation confirmed a significant decrease in the fraction of collecting duct cells that exhibited detectable AQP-2 labeling compared with control rats: in cortical collecting ducts, 40 ± 3.4 vs. 62 ± 1.8% of controls ( P < 0.05; n = 4) and in inner medullary collecting ducts, 58 ± 1.6 vs. 81 ± 1.3% of controls ( P < 0.05; n = 4). In parallel, a significant increase in the fraction of intercalated ([H + ]ATPase-positive) cells was shown. Urine output, whole kidney AQP-2 expression, cellular organization, and the fractions of principal and intercalated cells in cortex and inner medulla returned to control levels after 4 wk on a lithium-free diet following 4 wk on a lithium-containing diet. In conclusion, lithium treatment not only decreased AQP-2 expression, but dramatically and reversibly reduced the fraction of principal cells and altered the cellular organization in collecting ducts. These effects are likely to be important in lithium-induced nephrogenic diabetes insipidus.
nephrogenic diabetes insipidus; aquaporin; exchanger
Address for reprint requests and other correspondence: S. Nielsen, Water and Salt Research Center, Institute of Anatomy, Univ. of Aarhus, DK-8000 Aarhus, Denmark (E-mail: sn{at}ana.au.dk ).</description><subject>Animals</subject><subject>Antibodies</subject><subject>Aquaporin 2</subject><subject>Aquaporin 4</subject><subject>Aquaporin 6</subject><subject>Aquaporins - immunology</subject><subject>Aquaporins - metabolism</subject><subject>Carrier Proteins - immunology</subject><subject>Carrier Proteins - metabolism</subject><subject>Diabetes Insipidus, Nephrogenic - chemically induced</subject><subject>Diabetes Insipidus, Nephrogenic - metabolism</subject><subject>Down-Regulation - drug effects</subject><subject>Kidney Tubules, Collecting - drug effects</subject><subject>Kidney Tubules, Collecting - metabolism</subject><subject>Kidney Tubules, Collecting - ultrastructure</subject><subject>Lithium - pharmacology</subject><subject>Membrane Transport Proteins</subject><subject>Microscopy, Immunoelectron</subject><subject>Proton-Translocating ATPases - immunology</subject><subject>Proton-Translocating ATPases - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Recovery of Function</subject><subject>Urine</subject><issn>0363-6143</issn><issn>1522-1563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp1kMlOwzAURS0EoqXwAyyQfyDFQ-I6S1QoVKpgU9bGje3ExRkUJ4L8Pe4AXbF51ns-5y4uALcYTTFOyL3cNpl2booQYWxKEKJnYBw-SIQTRs_BGFFGI4ZjOgJX3m8RQjFh6SUY4Zhhynk6Bh_zQla59tBWcBfWO9nCrC6b2tvO1hWsDfy0qtJDuDqns85WOVR91u3xvdfKzsMv2xXQhWH7MrJVILSCr4_La3BhpPP65vhOwPviaT1_iVZvz8v5wyrKKJ91kckIMnjGiA5rOHG2oVynRG-UijkxmHOZGqNonOJEzTiVXGFjJMPK6DShdALIITdra-9bbUTT2lK2g8BI7OoSx7rEvi6xqytIdwep6TelVifl2E8AogNQ2Lz4sq0WTTF4W7s6H_4CCWciFvM0IYFP_-cXvXNr_d39iidPNMrQH3AHjkA</recordid><startdate>20040401</startdate><enddate>20040401</enddate><creator>Christensen, Birgitte Monster</creator><creator>Marples, David</creator><creator>Kim, Young-Hee</creator><creator>Wang, Weidong</creator><creator>Frokiaer, Jorgen</creator><creator>Nielsen, Soren</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></search><sort><creationdate>20040401</creationdate><title>Changes in cellular composition of kidney collecting duct cells in rats with lithium-induced NDI</title><author>Christensen, Birgitte Monster ; Marples, David ; Kim, Young-Hee ; Wang, Weidong ; Frokiaer, Jorgen ; Nielsen, Soren</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-fc20f1762e387c3886b38e92ebdd482f188a9ffd34915d783a8d1ffa61dfe9533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Aquaporin 2</topic><topic>Aquaporin 4</topic><topic>Aquaporin 6</topic><topic>Aquaporins - immunology</topic><topic>Aquaporins - metabolism</topic><topic>Carrier Proteins - immunology</topic><topic>Carrier Proteins - metabolism</topic><topic>Diabetes Insipidus, Nephrogenic - chemically induced</topic><topic>Diabetes Insipidus, Nephrogenic - metabolism</topic><topic>Down-Regulation - drug effects</topic><topic>Kidney Tubules, Collecting - drug effects</topic><topic>Kidney Tubules, Collecting - metabolism</topic><topic>Kidney Tubules, Collecting - ultrastructure</topic><topic>Lithium - pharmacology</topic><topic>Membrane Transport Proteins</topic><topic>Microscopy, Immunoelectron</topic><topic>Proton-Translocating ATPases - immunology</topic><topic>Proton-Translocating ATPases - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Recovery of Function</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Christensen, Birgitte Monster</creatorcontrib><creatorcontrib>Marples, David</creatorcontrib><creatorcontrib>Kim, Young-Hee</creatorcontrib><creatorcontrib>Wang, Weidong</creatorcontrib><creatorcontrib>Frokiaer, Jorgen</creatorcontrib><creatorcontrib>Nielsen, Soren</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>American Journal of Physiology: Cell Physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Christensen, Birgitte Monster</au><au>Marples, David</au><au>Kim, Young-Hee</au><au>Wang, Weidong</au><au>Frokiaer, Jorgen</au><au>Nielsen, Soren</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in cellular composition of kidney collecting duct cells in rats with lithium-induced NDI</atitle><jtitle>American Journal of Physiology: Cell Physiology</jtitle><addtitle>Am J Physiol Cell Physiol</addtitle><date>2004-04-01</date><risdate>2004</risdate><volume>286</volume><issue>4</issue><spage>C952</spage><epage>C964</epage><pages>C952-C964</pages><issn>0363-6143</issn><eissn>1522-1563</eissn><abstract>1 Water and Salt Research Center, 2 Institute of Anatomy, and 4 Institute of Experimental Clinical Research, University of Aarhus, DK-8000 Denmark; and 3 School of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom
Submitted 26 June 2003
; accepted in final form 4 November 2003
Lithium treatment for 4 wk caused severe polyuria, dramatic downregulation in aquaporin-2 (AQP-2) expression, and marked decrease in AQP-2 immunoreactivity with the appearance of a large number of cells without AQP-2 labeling in the collecting ducts after lithium treatment. Surprisingly, this was not all due to an increase in AQP-2-negative principal cells, because double immunolabeling revealed that the majority of the AQP-2-negative cells displayed [H + ]ATPase labeling, which identified them as intercalated cells. Moreover, multiple [H + ]ATPase-labeled cells were adjacent, which was never seen in control rats. Quantitation confirmed a significant decrease in the fraction of collecting duct cells that exhibited detectable AQP-2 labeling compared with control rats: in cortical collecting ducts, 40 ± 3.4 vs. 62 ± 1.8% of controls ( P < 0.05; n = 4) and in inner medullary collecting ducts, 58 ± 1.6 vs. 81 ± 1.3% of controls ( P < 0.05; n = 4). In parallel, a significant increase in the fraction of intercalated ([H + ]ATPase-positive) cells was shown. Urine output, whole kidney AQP-2 expression, cellular organization, and the fractions of principal and intercalated cells in cortex and inner medulla returned to control levels after 4 wk on a lithium-free diet following 4 wk on a lithium-containing diet. In conclusion, lithium treatment not only decreased AQP-2 expression, but dramatically and reversibly reduced the fraction of principal cells and altered the cellular organization in collecting ducts. These effects are likely to be important in lithium-induced nephrogenic diabetes insipidus.
nephrogenic diabetes insipidus; aquaporin; exchanger
Address for reprint requests and other correspondence: S. Nielsen, Water and Salt Research Center, Institute of Anatomy, Univ. of Aarhus, DK-8000 Aarhus, Denmark (E-mail: sn{at}ana.au.dk ).</abstract><cop>United States</cop><pmid>14613889</pmid><doi>10.1152/ajpcell.00266.2003</doi></addata></record> |
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subjects | Animals Antibodies Aquaporin 2 Aquaporin 4 Aquaporin 6 Aquaporins - immunology Aquaporins - metabolism Carrier Proteins - immunology Carrier Proteins - metabolism Diabetes Insipidus, Nephrogenic - chemically induced Diabetes Insipidus, Nephrogenic - metabolism Down-Regulation - drug effects Kidney Tubules, Collecting - drug effects Kidney Tubules, Collecting - metabolism Kidney Tubules, Collecting - ultrastructure Lithium - pharmacology Membrane Transport Proteins Microscopy, Immunoelectron Proton-Translocating ATPases - immunology Proton-Translocating ATPases - metabolism Rats Rats, Wistar Recovery of Function Urine |
title | Changes in cellular composition of kidney collecting duct cells in rats with lithium-induced NDI |
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