Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase

ABSTRACT Rapamycin, an immunosuppressant, is widely used in patients with kidney transplant. However, the therapeutic effects of rapamycin remain controversial. Additionally, previous studies have revealed deleterious effects of rapamycin predominantly when administered for ≥24 h. Few studies, howev...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The FASEB journal 2018-11, Vol.32 (11), p.6002-6018
Hauptverfasser: Li, Xinyuan, Zhu, Gongmin, Gou, Xin, He, Weiyang, Yin, Hubin, Yang, Xiaoyu, Li, Jie
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 6018
container_issue 11
container_start_page 6002
container_title The FASEB journal
container_volume 32
creator Li, Xinyuan
Zhu, Gongmin
Gou, Xin
He, Weiyang
Yin, Hubin
Yang, Xiaoyu
Li, Jie
description ABSTRACT Rapamycin, an immunosuppressant, is widely used in patients with kidney transplant. However, the therapeutic effects of rapamycin remain controversial. Additionally, previous studies have revealed deleterious effects of rapamycin predominantly when administered for ≥24 h. Few studies, however, have focused on the short term effects of rapamycin administered only during the initial reperfusion phase. As such, we designed this study to explore the potential effects and mechanisms of rapamycin under a specific therapeutic regimen in which rapamycin is mixed in the perfusate during the initial reperfusion phase (within 24 h). Interestingly, we found that rapamycin maintained renal function and attenuated ischemia‐reperfusion (I/R)‐induced apoptosis in vivo and in vitro during the initial reperfusion phase, especially at 8 h after reperfusion. Simultaneously, rapamycin activated autophagy and inhibited endoplasmic reticulum (ER) stress and 3 pathways of unfolding protein response: ATF6, PERK, and IRE1α. Interestingly, we further found that the protective effects of rapamycin were suppressed when autophagy was inhibited by chloroquine and 3‐methyladenine or when ER stress was induced by thapsigargin. Moreover, in terms of the regulatory effects of rapamycin, a negative‐feedback loop between autophagy and ER stress occurred, with autophagy inhibiting ER stress and increased ER stress promoting autophagy during the initial reperfusion phase of renal I/R injury. Our study provides evidence that immediate reperfusion with rapamycin during the initial reperfusion phase repairs renal function and reduces apoptosis via activating autophagy, which could further inhibit ER stress. These results suggest a novel treatment modality for application during the initial reperfusion phase of renal I/R injury caused by kidney transplantation.—Li, X., Zhu, G., Gou, X., He, W., Yin, H., Yang, X., Li, J. Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase. 32, 6002–6018 (2018). www.fasebj.org
doi_str_mv 10.1096/fj.201800299R
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2041630433</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2041630433</sourcerecordid><originalsourceid>FETCH-LOGICAL-c450R-d0c141ead8e4e508a67abcafba91d6888364549dd100542f42d8da53f6455b873</originalsourceid><addsrcrecordid>eNp90ctu1DAUBmALgehQWLJFXrJJOc7F44gVVJ0CqopUYB2d2MdTD4kT7ASUXR-hr9HX4klwNYV2xcoXff51rJ-xlwKOBNTyjd0d5SAUQF7XF4_YSlQFZFJJeMxWoOo8k7JQB-xZjDsAECDkU3aQ1-u1kFCs2M05bXFyP4lbItOi_s67YRj5YDnO0zBe4nbh6A0nb4axw9g7zQNNTs_d3PM4BYqRO88DjtgvOu3GMEykJzd4jlt0Pk7pgceOu6gvqXf4--o60EjBzvEWOb-bw8LNHJzfppObXMIPRZoi0nP2xGIX6cXdesi-bU6-Hn_Izj6ffjx-d5bpsoKLzIAWpSA0ikqqQKFcY6vRtlgLI5VShSyrsjZGAFRlbsvcKINVYdN11ap1cche73PTP37MFKemT4NT16GnYY5NDqWQBZRFkWi2pzoMMQayzRhcj2FpBDS37TR219y3k_yru-i57cn803_rSODtHvxyHS3_T2s2X97nm08P4v8AMvqiXA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2041630433</pqid></control><display><type>article</type><title>Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase</title><source>Wiley Online Library Journals Frontfile Complete</source><source>Alma/SFX Local Collection</source><creator>Li, Xinyuan ; Zhu, Gongmin ; Gou, Xin ; He, Weiyang ; Yin, Hubin ; Yang, Xiaoyu ; Li, Jie</creator><creatorcontrib>Li, Xinyuan ; Zhu, Gongmin ; Gou, Xin ; He, Weiyang ; Yin, Hubin ; Yang, Xiaoyu ; Li, Jie</creatorcontrib><description>ABSTRACT Rapamycin, an immunosuppressant, is widely used in patients with kidney transplant. However, the therapeutic effects of rapamycin remain controversial. Additionally, previous studies have revealed deleterious effects of rapamycin predominantly when administered for ≥24 h. Few studies, however, have focused on the short term effects of rapamycin administered only during the initial reperfusion phase. As such, we designed this study to explore the potential effects and mechanisms of rapamycin under a specific therapeutic regimen in which rapamycin is mixed in the perfusate during the initial reperfusion phase (within 24 h). Interestingly, we found that rapamycin maintained renal function and attenuated ischemia‐reperfusion (I/R)‐induced apoptosis in vivo and in vitro during the initial reperfusion phase, especially at 8 h after reperfusion. Simultaneously, rapamycin activated autophagy and inhibited endoplasmic reticulum (ER) stress and 3 pathways of unfolding protein response: ATF6, PERK, and IRE1α. Interestingly, we further found that the protective effects of rapamycin were suppressed when autophagy was inhibited by chloroquine and 3‐methyladenine or when ER stress was induced by thapsigargin. Moreover, in terms of the regulatory effects of rapamycin, a negative‐feedback loop between autophagy and ER stress occurred, with autophagy inhibiting ER stress and increased ER stress promoting autophagy during the initial reperfusion phase of renal I/R injury. Our study provides evidence that immediate reperfusion with rapamycin during the initial reperfusion phase repairs renal function and reduces apoptosis via activating autophagy, which could further inhibit ER stress. These results suggest a novel treatment modality for application during the initial reperfusion phase of renal I/R injury caused by kidney transplantation.—Li, X., Zhu, G., Gou, X., He, W., Yin, H., Yang, X., Li, J. Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase. 32, 6002–6018 (2018). www.fasebj.org</description><identifier>ISSN: 0892-6638</identifier><identifier>EISSN: 1530-6860</identifier><identifier>DOI: 10.1096/fj.201800299R</identifier><identifier>PMID: 29771603</identifier><language>eng</language><publisher>United States: Federation of American Societies for Experimental Biology</publisher><subject>acute kidney injury ; kidney transplantation ; sirolimus</subject><ispartof>The FASEB journal, 2018-11, Vol.32 (11), p.6002-6018</ispartof><rights>FASEB</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450R-d0c141ead8e4e508a67abcafba91d6888364549dd100542f42d8da53f6455b873</citedby><cites>FETCH-LOGICAL-c450R-d0c141ead8e4e508a67abcafba91d6888364549dd100542f42d8da53f6455b873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1096%2Ffj.201800299R$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1096%2Ffj.201800299R$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29771603$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xinyuan</creatorcontrib><creatorcontrib>Zhu, Gongmin</creatorcontrib><creatorcontrib>Gou, Xin</creatorcontrib><creatorcontrib>He, Weiyang</creatorcontrib><creatorcontrib>Yin, Hubin</creatorcontrib><creatorcontrib>Yang, Xiaoyu</creatorcontrib><creatorcontrib>Li, Jie</creatorcontrib><title>Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase</title><title>The FASEB journal</title><addtitle>FASEB J</addtitle><description>ABSTRACT Rapamycin, an immunosuppressant, is widely used in patients with kidney transplant. However, the therapeutic effects of rapamycin remain controversial. Additionally, previous studies have revealed deleterious effects of rapamycin predominantly when administered for ≥24 h. Few studies, however, have focused on the short term effects of rapamycin administered only during the initial reperfusion phase. As such, we designed this study to explore the potential effects and mechanisms of rapamycin under a specific therapeutic regimen in which rapamycin is mixed in the perfusate during the initial reperfusion phase (within 24 h). Interestingly, we found that rapamycin maintained renal function and attenuated ischemia‐reperfusion (I/R)‐induced apoptosis in vivo and in vitro during the initial reperfusion phase, especially at 8 h after reperfusion. Simultaneously, rapamycin activated autophagy and inhibited endoplasmic reticulum (ER) stress and 3 pathways of unfolding protein response: ATF6, PERK, and IRE1α. Interestingly, we further found that the protective effects of rapamycin were suppressed when autophagy was inhibited by chloroquine and 3‐methyladenine or when ER stress was induced by thapsigargin. Moreover, in terms of the regulatory effects of rapamycin, a negative‐feedback loop between autophagy and ER stress occurred, with autophagy inhibiting ER stress and increased ER stress promoting autophagy during the initial reperfusion phase of renal I/R injury. Our study provides evidence that immediate reperfusion with rapamycin during the initial reperfusion phase repairs renal function and reduces apoptosis via activating autophagy, which could further inhibit ER stress. These results suggest a novel treatment modality for application during the initial reperfusion phase of renal I/R injury caused by kidney transplantation.—Li, X., Zhu, G., Gou, X., He, W., Yin, H., Yang, X., Li, J. Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase. 32, 6002–6018 (2018). www.fasebj.org</description><subject>acute kidney injury</subject><subject>kidney transplantation</subject><subject>sirolimus</subject><issn>0892-6638</issn><issn>1530-6860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp90ctu1DAUBmALgehQWLJFXrJJOc7F44gVVJ0CqopUYB2d2MdTD4kT7ASUXR-hr9HX4klwNYV2xcoXff51rJ-xlwKOBNTyjd0d5SAUQF7XF4_YSlQFZFJJeMxWoOo8k7JQB-xZjDsAECDkU3aQ1-u1kFCs2M05bXFyP4lbItOi_s67YRj5YDnO0zBe4nbh6A0nb4axw9g7zQNNTs_d3PM4BYqRO88DjtgvOu3GMEykJzd4jlt0Pk7pgceOu6gvqXf4--o60EjBzvEWOb-bw8LNHJzfppObXMIPRZoi0nP2xGIX6cXdesi-bU6-Hn_Izj6ffjx-d5bpsoKLzIAWpSA0ikqqQKFcY6vRtlgLI5VShSyrsjZGAFRlbsvcKINVYdN11ap1cche73PTP37MFKemT4NT16GnYY5NDqWQBZRFkWi2pzoMMQayzRhcj2FpBDS37TR219y3k_yru-i57cn803_rSODtHvxyHS3_T2s2X97nm08P4v8AMvqiXA</recordid><startdate>201811</startdate><enddate>201811</enddate><creator>Li, Xinyuan</creator><creator>Zhu, Gongmin</creator><creator>Gou, Xin</creator><creator>He, Weiyang</creator><creator>Yin, Hubin</creator><creator>Yang, Xiaoyu</creator><creator>Li, Jie</creator><general>Federation of American Societies for Experimental Biology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201811</creationdate><title>Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase</title><author>Li, Xinyuan ; Zhu, Gongmin ; Gou, Xin ; He, Weiyang ; Yin, Hubin ; Yang, Xiaoyu ; Li, Jie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450R-d0c141ead8e4e508a67abcafba91d6888364549dd100542f42d8da53f6455b873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>acute kidney injury</topic><topic>kidney transplantation</topic><topic>sirolimus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xinyuan</creatorcontrib><creatorcontrib>Zhu, Gongmin</creatorcontrib><creatorcontrib>Gou, Xin</creatorcontrib><creatorcontrib>He, Weiyang</creatorcontrib><creatorcontrib>Yin, Hubin</creatorcontrib><creatorcontrib>Yang, Xiaoyu</creatorcontrib><creatorcontrib>Li, Jie</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The FASEB journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xinyuan</au><au>Zhu, Gongmin</au><au>Gou, Xin</au><au>He, Weiyang</au><au>Yin, Hubin</au><au>Yang, Xiaoyu</au><au>Li, Jie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase</atitle><jtitle>The FASEB journal</jtitle><addtitle>FASEB J</addtitle><date>2018-11</date><risdate>2018</risdate><volume>32</volume><issue>11</issue><spage>6002</spage><epage>6018</epage><pages>6002-6018</pages><issn>0892-6638</issn><eissn>1530-6860</eissn><abstract>ABSTRACT Rapamycin, an immunosuppressant, is widely used in patients with kidney transplant. However, the therapeutic effects of rapamycin remain controversial. Additionally, previous studies have revealed deleterious effects of rapamycin predominantly when administered for ≥24 h. Few studies, however, have focused on the short term effects of rapamycin administered only during the initial reperfusion phase. As such, we designed this study to explore the potential effects and mechanisms of rapamycin under a specific therapeutic regimen in which rapamycin is mixed in the perfusate during the initial reperfusion phase (within 24 h). Interestingly, we found that rapamycin maintained renal function and attenuated ischemia‐reperfusion (I/R)‐induced apoptosis in vivo and in vitro during the initial reperfusion phase, especially at 8 h after reperfusion. Simultaneously, rapamycin activated autophagy and inhibited endoplasmic reticulum (ER) stress and 3 pathways of unfolding protein response: ATF6, PERK, and IRE1α. Interestingly, we further found that the protective effects of rapamycin were suppressed when autophagy was inhibited by chloroquine and 3‐methyladenine or when ER stress was induced by thapsigargin. Moreover, in terms of the regulatory effects of rapamycin, a negative‐feedback loop between autophagy and ER stress occurred, with autophagy inhibiting ER stress and increased ER stress promoting autophagy during the initial reperfusion phase of renal I/R injury. Our study provides evidence that immediate reperfusion with rapamycin during the initial reperfusion phase repairs renal function and reduces apoptosis via activating autophagy, which could further inhibit ER stress. These results suggest a novel treatment modality for application during the initial reperfusion phase of renal I/R injury caused by kidney transplantation.—Li, X., Zhu, G., Gou, X., He, W., Yin, H., Yang, X., Li, J. Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase. 32, 6002–6018 (2018). www.fasebj.org</abstract><cop>United States</cop><pub>Federation of American Societies for Experimental Biology</pub><pmid>29771603</pmid><doi>10.1096/fj.201800299R</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0892-6638
ispartof The FASEB journal, 2018-11, Vol.32 (11), p.6002-6018
issn 0892-6638
1530-6860
language eng
recordid cdi_proquest_miscellaneous_2041630433
source Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects acute kidney injury
kidney transplantation
sirolimus
title Negative feedback loop of autophagy and endoplasmic reticulum stress in rapamycin protection against renal ischemia‐reperfusion injury during initial reperfusion phase
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T04%3A25%3A17IST&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=Negative%20feedback%20loop%20of%20autophagy%20and%20endoplasmic%20reticulum%20stress%20in%20rapamycin%20protection%20against%20renal%20ischemia%E2%80%90reperfusion%20injury%20during%20initial%20reperfusion%20phase&rft.jtitle=The%20FASEB%20journal&rft.au=Li,%20Xinyuan&rft.date=2018-11&rft.volume=32&rft.issue=11&rft.spage=6002&rft.epage=6018&rft.pages=6002-6018&rft.issn=0892-6638&rft.eissn=1530-6860&rft_id=info:doi/10.1096/fj.201800299R&rft_dat=%3Cproquest_cross%3E2041630433%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=2041630433&rft_id=info:pmid/29771603&rfr_iscdi=true