Involvement of neutrophil gelatinase-associated lipocalin and osteopontin in renal tubular regeneration and interstitial fibrosis after cisplatin-induced renal failure
The kidney has a capacity to recover from ischemic or toxic insults that result in cell death, and timely tissue repair of affected renal tubules may arrest progression of injury, leading to regression of injury and paving the way for recovery. To investigate the roles of neutrophil gelatinase-assoc...
Gespeichert in:
Veröffentlicht in: | Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie 2014-09, Vol.66 (7), p.301-311 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 311 |
---|---|
container_issue | 7 |
container_start_page | 301 |
container_title | Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie |
container_volume | 66 |
creator | Kashiwagi, Emi Tonomura, Yutaka Kondo, Chiaki Masuno, Koichi Fujisawa, Kae Tsuchiya, Noriko Matsushima, Shuuichi Torii, Mikinori Takasu, Nobuo Izawa, Takeshi Kuwamura, Mitsuru Yamate, Jyoji |
description | The kidney has a capacity to recover from ischemic or toxic insults that result in cell death, and timely tissue repair of affected renal tubules may arrest progression of injury, leading to regression of injury and paving the way for recovery. To investigate the roles of neutrophil gelatinase-associated lipocalin (NGAL/lcn2) and osteopontin (OPN/spp1) during renal regeneration, the expression patterns of NGAL and OPN in the cisplatin-induced rat renal failure model were examined. NGAL expression was increased from day 1 after injection; it was seen mainly in the completely regenerating proximal tubules of the cortico-medullary junction on days 3–35; however, the expression was not seen in abnormally dilated or atrophied renal tubules surrounded by fibrotic lesions. On the other hand, OPN expression was increased from day 5 and the increased expression developed exclusively in the abnormal renal tubules. NGAL expression level well correlated with the proliferating activity in the regenerating renal epithelial cells, whereas OPN significantly correlated with the α-smooth muscle actin-positive myofibroblast appearance, expression of transforming growth factor (TGF)-β1, and the number of CD68-positive macrophages. Interestingly, rat renal epithelial cell line (NRK-52E) treated with TGF-β1 decreased NGAL expression, but increased OPN expression in a dose-dependent manner. Because increases of TGF-β1, myofibroblasts and macrophages contribute to progressive interstitial renal fibrosis, OPN may be involved in the pathogenesis of fibrosis; on the contrary, NGAL may play a role in tubular regeneration after injury. Expression analysis of NGAL and OPN would be useful to investigate the tubule damage in renal-toxicity. |
doi_str_mv | 10.1016/j.etp.2014.04.007 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1543999245</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0940299314000554</els_id><sourcerecordid>1543999245</sourcerecordid><originalsourceid>FETCH-LOGICAL-c522t-51f704e3b3814a13cd994505feae8facd96f43b2f747f8f472befcbb1d7ede2f3</originalsourceid><addsrcrecordid>eNp9kU1uFDEQhS0EIpPAAdggL9n04L-eHosVipIQKRKbsLbc7nKokcdubPdInCjXxKEDy0hPsqr01SuVHyEfONtyxnefD1uo81YwrrasiQ2vyIbv-L7jSsrXZMO0Yp3QWp6R81IOjAmme_6WnAmluRiU3pDH23hK4QRHiJUmTyMsNaf5Jwb6AMFWjLZAZ0tJDm2FiQack7MBI7VxoqlUSHOKjaNNGaINtC7jEmxu1QNEyM0krTTGCrlUrNgoj2NOBQu1vnWpwzL_3ddhnBbXNq1m3mJYMrwjb7wNBd4_vxfkx_XV_eW37u77ze3l17vO9ULUrud-YArkKPdcWS7dpLXqWe_Bwt7bVu68kqPwgxr83qtBjODdOPJpgAmElxfk0-o75_RrgVLNEYuDEGyEtBTDeyW11kL1DeUr6todJYM3c8ajzb8NZ-YpH3MwLR_zlI9hTWxoMx-f7ZfxCNP_iX-BNODLCkA78oSQTXEIsf0HZnDVTAlfsP8DMG6ngQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1543999245</pqid></control><display><type>article</type><title>Involvement of neutrophil gelatinase-associated lipocalin and osteopontin in renal tubular regeneration and interstitial fibrosis after cisplatin-induced renal failure</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Kashiwagi, Emi ; Tonomura, Yutaka ; Kondo, Chiaki ; Masuno, Koichi ; Fujisawa, Kae ; Tsuchiya, Noriko ; Matsushima, Shuuichi ; Torii, Mikinori ; Takasu, Nobuo ; Izawa, Takeshi ; Kuwamura, Mitsuru ; Yamate, Jyoji</creator><creatorcontrib>Kashiwagi, Emi ; Tonomura, Yutaka ; Kondo, Chiaki ; Masuno, Koichi ; Fujisawa, Kae ; Tsuchiya, Noriko ; Matsushima, Shuuichi ; Torii, Mikinori ; Takasu, Nobuo ; Izawa, Takeshi ; Kuwamura, Mitsuru ; Yamate, Jyoji</creatorcontrib><description>The kidney has a capacity to recover from ischemic or toxic insults that result in cell death, and timely tissue repair of affected renal tubules may arrest progression of injury, leading to regression of injury and paving the way for recovery. To investigate the roles of neutrophil gelatinase-associated lipocalin (NGAL/lcn2) and osteopontin (OPN/spp1) during renal regeneration, the expression patterns of NGAL and OPN in the cisplatin-induced rat renal failure model were examined. NGAL expression was increased from day 1 after injection; it was seen mainly in the completely regenerating proximal tubules of the cortico-medullary junction on days 3–35; however, the expression was not seen in abnormally dilated or atrophied renal tubules surrounded by fibrotic lesions. On the other hand, OPN expression was increased from day 5 and the increased expression developed exclusively in the abnormal renal tubules. NGAL expression level well correlated with the proliferating activity in the regenerating renal epithelial cells, whereas OPN significantly correlated with the α-smooth muscle actin-positive myofibroblast appearance, expression of transforming growth factor (TGF)-β1, and the number of CD68-positive macrophages. Interestingly, rat renal epithelial cell line (NRK-52E) treated with TGF-β1 decreased NGAL expression, but increased OPN expression in a dose-dependent manner. Because increases of TGF-β1, myofibroblasts and macrophages contribute to progressive interstitial renal fibrosis, OPN may be involved in the pathogenesis of fibrosis; on the contrary, NGAL may play a role in tubular regeneration after injury. Expression analysis of NGAL and OPN would be useful to investigate the tubule damage in renal-toxicity.</description><identifier>ISSN: 0940-2993</identifier><identifier>EISSN: 1618-1433</identifier><identifier>DOI: 10.1016/j.etp.2014.04.007</identifier><identifier>PMID: 24912749</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Acute-Phase Proteins - metabolism ; Animals ; Antineoplastic Agents - toxicity ; Cisplatin ; Cisplatin - toxicity ; Fibrosis ; Kidney Tubules - drug effects ; Kidney Tubules - metabolism ; Kidney Tubules - pathology ; Lipocalins - metabolism ; Male ; Nephritis, Interstitial - chemically induced ; Nephritis, Interstitial - metabolism ; Nephritis, Interstitial - pathology ; Neutrophil gelatinase-associated lipocalin ; Osteopontin ; Osteopontin - metabolism ; Proto-Oncogene Proteins - metabolism ; Rats, Inbred F344 ; Real-Time Polymerase Chain Reaction ; Regeneration ; Renal failure ; Renal Insufficiency - chemically induced ; Renal Insufficiency - metabolism ; Renal Insufficiency - pathology</subject><ispartof>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie, 2014-09, Vol.66 (7), p.301-311</ispartof><rights>2014 Elsevier GmbH</rights><rights>Copyright © 2014 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-51f704e3b3814a13cd994505feae8facd96f43b2f747f8f472befcbb1d7ede2f3</citedby><cites>FETCH-LOGICAL-c522t-51f704e3b3814a13cd994505feae8facd96f43b2f747f8f472befcbb1d7ede2f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0940299314000554$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24912749$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kashiwagi, Emi</creatorcontrib><creatorcontrib>Tonomura, Yutaka</creatorcontrib><creatorcontrib>Kondo, Chiaki</creatorcontrib><creatorcontrib>Masuno, Koichi</creatorcontrib><creatorcontrib>Fujisawa, Kae</creatorcontrib><creatorcontrib>Tsuchiya, Noriko</creatorcontrib><creatorcontrib>Matsushima, Shuuichi</creatorcontrib><creatorcontrib>Torii, Mikinori</creatorcontrib><creatorcontrib>Takasu, Nobuo</creatorcontrib><creatorcontrib>Izawa, Takeshi</creatorcontrib><creatorcontrib>Kuwamura, Mitsuru</creatorcontrib><creatorcontrib>Yamate, Jyoji</creatorcontrib><title>Involvement of neutrophil gelatinase-associated lipocalin and osteopontin in renal tubular regeneration and interstitial fibrosis after cisplatin-induced renal failure</title><title>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</title><addtitle>Exp Toxicol Pathol</addtitle><description>The kidney has a capacity to recover from ischemic or toxic insults that result in cell death, and timely tissue repair of affected renal tubules may arrest progression of injury, leading to regression of injury and paving the way for recovery. To investigate the roles of neutrophil gelatinase-associated lipocalin (NGAL/lcn2) and osteopontin (OPN/spp1) during renal regeneration, the expression patterns of NGAL and OPN in the cisplatin-induced rat renal failure model were examined. NGAL expression was increased from day 1 after injection; it was seen mainly in the completely regenerating proximal tubules of the cortico-medullary junction on days 3–35; however, the expression was not seen in abnormally dilated or atrophied renal tubules surrounded by fibrotic lesions. On the other hand, OPN expression was increased from day 5 and the increased expression developed exclusively in the abnormal renal tubules. NGAL expression level well correlated with the proliferating activity in the regenerating renal epithelial cells, whereas OPN significantly correlated with the α-smooth muscle actin-positive myofibroblast appearance, expression of transforming growth factor (TGF)-β1, and the number of CD68-positive macrophages. Interestingly, rat renal epithelial cell line (NRK-52E) treated with TGF-β1 decreased NGAL expression, but increased OPN expression in a dose-dependent manner. Because increases of TGF-β1, myofibroblasts and macrophages contribute to progressive interstitial renal fibrosis, OPN may be involved in the pathogenesis of fibrosis; on the contrary, NGAL may play a role in tubular regeneration after injury. Expression analysis of NGAL and OPN would be useful to investigate the tubule damage in renal-toxicity.</description><subject>Acute-Phase Proteins - metabolism</subject><subject>Animals</subject><subject>Antineoplastic Agents - toxicity</subject><subject>Cisplatin</subject><subject>Cisplatin - toxicity</subject><subject>Fibrosis</subject><subject>Kidney Tubules - drug effects</subject><subject>Kidney Tubules - metabolism</subject><subject>Kidney Tubules - pathology</subject><subject>Lipocalins - metabolism</subject><subject>Male</subject><subject>Nephritis, Interstitial - chemically induced</subject><subject>Nephritis, Interstitial - metabolism</subject><subject>Nephritis, Interstitial - pathology</subject><subject>Neutrophil gelatinase-associated lipocalin</subject><subject>Osteopontin</subject><subject>Osteopontin - metabolism</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Rats, Inbred F344</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Regeneration</subject><subject>Renal failure</subject><subject>Renal Insufficiency - chemically induced</subject><subject>Renal Insufficiency - metabolism</subject><subject>Renal Insufficiency - pathology</subject><issn>0940-2993</issn><issn>1618-1433</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1uFDEQhS0EIpPAAdggL9n04L-eHosVipIQKRKbsLbc7nKokcdubPdInCjXxKEDy0hPsqr01SuVHyEfONtyxnefD1uo81YwrrasiQ2vyIbv-L7jSsrXZMO0Yp3QWp6R81IOjAmme_6WnAmluRiU3pDH23hK4QRHiJUmTyMsNaf5Jwb6AMFWjLZAZ0tJDm2FiQack7MBI7VxoqlUSHOKjaNNGaINtC7jEmxu1QNEyM0krTTGCrlUrNgoj2NOBQu1vnWpwzL_3ddhnBbXNq1m3mJYMrwjb7wNBd4_vxfkx_XV_eW37u77ze3l17vO9ULUrud-YArkKPdcWS7dpLXqWe_Bwt7bVu68kqPwgxr83qtBjODdOPJpgAmElxfk0-o75_RrgVLNEYuDEGyEtBTDeyW11kL1DeUr6todJYM3c8ajzb8NZ-YpH3MwLR_zlI9hTWxoMx-f7ZfxCNP_iX-BNODLCkA78oSQTXEIsf0HZnDVTAlfsP8DMG6ngQ</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Kashiwagi, Emi</creator><creator>Tonomura, Yutaka</creator><creator>Kondo, Chiaki</creator><creator>Masuno, Koichi</creator><creator>Fujisawa, Kae</creator><creator>Tsuchiya, Noriko</creator><creator>Matsushima, Shuuichi</creator><creator>Torii, Mikinori</creator><creator>Takasu, Nobuo</creator><creator>Izawa, Takeshi</creator><creator>Kuwamura, Mitsuru</creator><creator>Yamate, Jyoji</creator><general>Elsevier GmbH</general><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20140901</creationdate><title>Involvement of neutrophil gelatinase-associated lipocalin and osteopontin in renal tubular regeneration and interstitial fibrosis after cisplatin-induced renal failure</title><author>Kashiwagi, Emi ; Tonomura, Yutaka ; Kondo, Chiaki ; Masuno, Koichi ; Fujisawa, Kae ; Tsuchiya, Noriko ; Matsushima, Shuuichi ; Torii, Mikinori ; Takasu, Nobuo ; Izawa, Takeshi ; Kuwamura, Mitsuru ; Yamate, Jyoji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c522t-51f704e3b3814a13cd994505feae8facd96f43b2f747f8f472befcbb1d7ede2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acute-Phase Proteins - metabolism</topic><topic>Animals</topic><topic>Antineoplastic Agents - toxicity</topic><topic>Cisplatin</topic><topic>Cisplatin - toxicity</topic><topic>Fibrosis</topic><topic>Kidney Tubules - drug effects</topic><topic>Kidney Tubules - metabolism</topic><topic>Kidney Tubules - pathology</topic><topic>Lipocalins - metabolism</topic><topic>Male</topic><topic>Nephritis, Interstitial - chemically induced</topic><topic>Nephritis, Interstitial - metabolism</topic><topic>Nephritis, Interstitial - pathology</topic><topic>Neutrophil gelatinase-associated lipocalin</topic><topic>Osteopontin</topic><topic>Osteopontin - metabolism</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Rats, Inbred F344</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Regeneration</topic><topic>Renal failure</topic><topic>Renal Insufficiency - chemically induced</topic><topic>Renal Insufficiency - metabolism</topic><topic>Renal Insufficiency - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kashiwagi, Emi</creatorcontrib><creatorcontrib>Tonomura, Yutaka</creatorcontrib><creatorcontrib>Kondo, Chiaki</creatorcontrib><creatorcontrib>Masuno, Koichi</creatorcontrib><creatorcontrib>Fujisawa, Kae</creatorcontrib><creatorcontrib>Tsuchiya, Noriko</creatorcontrib><creatorcontrib>Matsushima, Shuuichi</creatorcontrib><creatorcontrib>Torii, Mikinori</creatorcontrib><creatorcontrib>Takasu, Nobuo</creatorcontrib><creatorcontrib>Izawa, Takeshi</creatorcontrib><creatorcontrib>Kuwamura, Mitsuru</creatorcontrib><creatorcontrib>Yamate, Jyoji</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kashiwagi, Emi</au><au>Tonomura, Yutaka</au><au>Kondo, Chiaki</au><au>Masuno, Koichi</au><au>Fujisawa, Kae</au><au>Tsuchiya, Noriko</au><au>Matsushima, Shuuichi</au><au>Torii, Mikinori</au><au>Takasu, Nobuo</au><au>Izawa, Takeshi</au><au>Kuwamura, Mitsuru</au><au>Yamate, Jyoji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Involvement of neutrophil gelatinase-associated lipocalin and osteopontin in renal tubular regeneration and interstitial fibrosis after cisplatin-induced renal failure</atitle><jtitle>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</jtitle><addtitle>Exp Toxicol Pathol</addtitle><date>2014-09-01</date><risdate>2014</risdate><volume>66</volume><issue>7</issue><spage>301</spage><epage>311</epage><pages>301-311</pages><issn>0940-2993</issn><eissn>1618-1433</eissn><abstract>The kidney has a capacity to recover from ischemic or toxic insults that result in cell death, and timely tissue repair of affected renal tubules may arrest progression of injury, leading to regression of injury and paving the way for recovery. To investigate the roles of neutrophil gelatinase-associated lipocalin (NGAL/lcn2) and osteopontin (OPN/spp1) during renal regeneration, the expression patterns of NGAL and OPN in the cisplatin-induced rat renal failure model were examined. NGAL expression was increased from day 1 after injection; it was seen mainly in the completely regenerating proximal tubules of the cortico-medullary junction on days 3–35; however, the expression was not seen in abnormally dilated or atrophied renal tubules surrounded by fibrotic lesions. On the other hand, OPN expression was increased from day 5 and the increased expression developed exclusively in the abnormal renal tubules. NGAL expression level well correlated with the proliferating activity in the regenerating renal epithelial cells, whereas OPN significantly correlated with the α-smooth muscle actin-positive myofibroblast appearance, expression of transforming growth factor (TGF)-β1, and the number of CD68-positive macrophages. Interestingly, rat renal epithelial cell line (NRK-52E) treated with TGF-β1 decreased NGAL expression, but increased OPN expression in a dose-dependent manner. Because increases of TGF-β1, myofibroblasts and macrophages contribute to progressive interstitial renal fibrosis, OPN may be involved in the pathogenesis of fibrosis; on the contrary, NGAL may play a role in tubular regeneration after injury. Expression analysis of NGAL and OPN would be useful to investigate the tubule damage in renal-toxicity.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>24912749</pmid><doi>10.1016/j.etp.2014.04.007</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0940-2993 |
ispartof | Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie, 2014-09, Vol.66 (7), p.301-311 |
issn | 0940-2993 1618-1433 |
language | eng |
recordid | cdi_proquest_miscellaneous_1543999245 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Acute-Phase Proteins - metabolism Animals Antineoplastic Agents - toxicity Cisplatin Cisplatin - toxicity Fibrosis Kidney Tubules - drug effects Kidney Tubules - metabolism Kidney Tubules - pathology Lipocalins - metabolism Male Nephritis, Interstitial - chemically induced Nephritis, Interstitial - metabolism Nephritis, Interstitial - pathology Neutrophil gelatinase-associated lipocalin Osteopontin Osteopontin - metabolism Proto-Oncogene Proteins - metabolism Rats, Inbred F344 Real-Time Polymerase Chain Reaction Regeneration Renal failure Renal Insufficiency - chemically induced Renal Insufficiency - metabolism Renal Insufficiency - pathology |
title | Involvement of neutrophil gelatinase-associated lipocalin and osteopontin in renal tubular regeneration and interstitial fibrosis after cisplatin-induced renal failure |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T19%3A38%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Involvement%20of%20neutrophil%20gelatinase-associated%20lipocalin%20and%20osteopontin%20in%20renal%20tubular%20regeneration%20and%20interstitial%20fibrosis%20after%20cisplatin-induced%20renal%20failure&rft.jtitle=Experimental%20and%20toxicologic%20pathology%20:%20official%20journal%20of%20the%20Gesellschaft%20f%C3%BCr%20Toxikologische%20Pathologie&rft.au=Kashiwagi,%20Emi&rft.date=2014-09-01&rft.volume=66&rft.issue=7&rft.spage=301&rft.epage=311&rft.pages=301-311&rft.issn=0940-2993&rft.eissn=1618-1433&rft_id=info:doi/10.1016/j.etp.2014.04.007&rft_dat=%3Cproquest_cross%3E1543999245%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1543999245&rft_id=info:pmid/24912749&rft_els_id=S0940299314000554&rfr_iscdi=true |