Adipose delivered stem cells protect liver after ischemia-reperfusion injury by controlling autophagy
: Ischemia-reperfusion(I/R) injury is an unavoidable side effect of liver surgery and transplantation. A potentially useful tool for cellular therapy and tissue engineering is adipose-derived stem cells (ADSCs).The process of autophagy is used by the cell to break down inappropriate molecules.The st...
Gespeichert in:
Veröffentlicht in: | Injury 2023-08, Vol.54 (8), p.110839-110839, Article 110839 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 110839 |
---|---|
container_issue | 8 |
container_start_page | 110839 |
container_title | Injury |
container_volume | 54 |
creator | Kartal, Bahar Alimoğulları, Ebru Elçi, Pınar Demir, Hazal |
description | : Ischemia-reperfusion(I/R) injury is an unavoidable side effect of liver surgery and transplantation. A potentially useful tool for cellular therapy and tissue engineering is adipose-derived stem cells (ADSCs).The process of autophagy is used by the cell to break down inappropriate molecules.The study's goal was to examine the impact of ADSCs on the autophagic pathway after rat hepatic ischemia-reperfusion injury.
: Thirty male rats used in our study were divided into control, ADSC, ischemia, I/R, and I/R+ ADSC groups (n = 6). Liver tissues were stained with hematoxylin-eosin and histological changes were evaluated with Suzuki scoring. Immunoexpressions of transforming growth factor (TGF-β) and autophagy markers LC3B, p62 were analyzed using the immunohistochemical method.
: As a result of histological evaluation the ischemia and I/R groups displayed sinusoid congestion, vacuolization, and necrosis in liver tissues. We showed that the immunostaining of LC3B and TGF- β were elevated, and p62 decreased in the rat liver from ischemia and I/R groups when compared to the control group.
: ADSCs reduced the excessive level of autophagy and structural damage to hepatocytes and the pathological alterations in the liver after ıschemia-reperfusion injury. |
doi_str_mv | 10.1016/j.injury.2023.110839 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2820971340</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0020138323005077</els_id><sourcerecordid>2820971340</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-27a06da77e03ca107ee98efe8d91e3c57c35a7c47c2ecf79fabaa64a97e27dc13</originalsourceid><addsrcrecordid>eNp9kL1OwzAURi0EglJ4A4Q8sqRc26FOFqQK8SdVYoHZcu2b1lUSBzup1LfHJcDIYg8-1_f7DiFXDGYM2Px2O3Ptdgj7GQcuZoxBIcojMmGFLDPgc3lMJgAcMiYKcUbOY9wCMAlCnJIzIXleMCYmBBfWdT4itVi7HQa0NPbYUIN1HWkXfI-mp99PVFd9Ol00G2yczgJ2GKohOt_SMQpd7anxbR98Xbt2TfXQ-26j1_sLclLpOuLlzz0lH0-P7w8v2fLt-fVhscyMuJN9xqWGudVSIgijGUjEssAKC1syFOZOJkxLk0vD0VSyrPRK63muS4lcWsPElNyM_6bgnwPGXjUpbqqiW_RDVLzgUEomckhoPqIm-BgDVqoLrtFhrxiog2C1VWMrdRCsRsFp7Ppnw7Bq0P4N_RpNwP0IYOq5cxhUNA5bg9aFpFJZ7_7f8AVM8JF7</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2820971340</pqid></control><display><type>article</type><title>Adipose delivered stem cells protect liver after ischemia-reperfusion injury by controlling autophagy</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Kartal, Bahar ; Alimoğulları, Ebru ; Elçi, Pınar ; Demir, Hazal</creator><creatorcontrib>Kartal, Bahar ; Alimoğulları, Ebru ; Elçi, Pınar ; Demir, Hazal</creatorcontrib><description>: Ischemia-reperfusion(I/R) injury is an unavoidable side effect of liver surgery and transplantation. A potentially useful tool for cellular therapy and tissue engineering is adipose-derived stem cells (ADSCs).The process of autophagy is used by the cell to break down inappropriate molecules.The study's goal was to examine the impact of ADSCs on the autophagic pathway after rat hepatic ischemia-reperfusion injury.
: Thirty male rats used in our study were divided into control, ADSC, ischemia, I/R, and I/R+ ADSC groups (n = 6). Liver tissues were stained with hematoxylin-eosin and histological changes were evaluated with Suzuki scoring. Immunoexpressions of transforming growth factor (TGF-β) and autophagy markers LC3B, p62 were analyzed using the immunohistochemical method.
: As a result of histological evaluation the ischemia and I/R groups displayed sinusoid congestion, vacuolization, and necrosis in liver tissues. We showed that the immunostaining of LC3B and TGF- β were elevated, and p62 decreased in the rat liver from ischemia and I/R groups when compared to the control group.
: ADSCs reduced the excessive level of autophagy and structural damage to hepatocytes and the pathological alterations in the liver after ıschemia-reperfusion injury.</description><identifier>ISSN: 0020-1383</identifier><identifier>EISSN: 1879-0267</identifier><identifier>DOI: 10.1016/j.injury.2023.110839</identifier><identifier>PMID: 37248113</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adipose Tissue ; Adipose-derived stem cells(ADSCs) ; Animals ; Autophagy ; Histopathology ; Ischemia ; Ischemia-reperfusion injury ; Liver ; Liver - pathology ; Male ; Rats ; Reperfusion Injury - metabolism ; Stem Cells - metabolism</subject><ispartof>Injury, 2023-08, Vol.54 (8), p.110839-110839, Article 110839</ispartof><rights>2023</rights><rights>Copyright © 2023. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c357t-27a06da77e03ca107ee98efe8d91e3c57c35a7c47c2ecf79fabaa64a97e27dc13</cites><orcidid>0000-0001-9558-4122</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.injury.2023.110839$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37248113$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kartal, Bahar</creatorcontrib><creatorcontrib>Alimoğulları, Ebru</creatorcontrib><creatorcontrib>Elçi, Pınar</creatorcontrib><creatorcontrib>Demir, Hazal</creatorcontrib><title>Adipose delivered stem cells protect liver after ischemia-reperfusion injury by controlling autophagy</title><title>Injury</title><addtitle>Injury</addtitle><description>: Ischemia-reperfusion(I/R) injury is an unavoidable side effect of liver surgery and transplantation. A potentially useful tool for cellular therapy and tissue engineering is adipose-derived stem cells (ADSCs).The process of autophagy is used by the cell to break down inappropriate molecules.The study's goal was to examine the impact of ADSCs on the autophagic pathway after rat hepatic ischemia-reperfusion injury.
: Thirty male rats used in our study were divided into control, ADSC, ischemia, I/R, and I/R+ ADSC groups (n = 6). Liver tissues were stained with hematoxylin-eosin and histological changes were evaluated with Suzuki scoring. Immunoexpressions of transforming growth factor (TGF-β) and autophagy markers LC3B, p62 were analyzed using the immunohistochemical method.
: As a result of histological evaluation the ischemia and I/R groups displayed sinusoid congestion, vacuolization, and necrosis in liver tissues. We showed that the immunostaining of LC3B and TGF- β were elevated, and p62 decreased in the rat liver from ischemia and I/R groups when compared to the control group.
: ADSCs reduced the excessive level of autophagy and structural damage to hepatocytes and the pathological alterations in the liver after ıschemia-reperfusion injury.</description><subject>Adipose Tissue</subject><subject>Adipose-derived stem cells(ADSCs)</subject><subject>Animals</subject><subject>Autophagy</subject><subject>Histopathology</subject><subject>Ischemia</subject><subject>Ischemia-reperfusion injury</subject><subject>Liver</subject><subject>Liver - pathology</subject><subject>Male</subject><subject>Rats</subject><subject>Reperfusion Injury - metabolism</subject><subject>Stem Cells - metabolism</subject><issn>0020-1383</issn><issn>1879-0267</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kL1OwzAURi0EglJ4A4Q8sqRc26FOFqQK8SdVYoHZcu2b1lUSBzup1LfHJcDIYg8-1_f7DiFXDGYM2Px2O3Ptdgj7GQcuZoxBIcojMmGFLDPgc3lMJgAcMiYKcUbOY9wCMAlCnJIzIXleMCYmBBfWdT4itVi7HQa0NPbYUIN1HWkXfI-mp99PVFd9Ol00G2yczgJ2GKohOt_SMQpd7anxbR98Xbt2TfXQ-26j1_sLclLpOuLlzz0lH0-P7w8v2fLt-fVhscyMuJN9xqWGudVSIgijGUjEssAKC1syFOZOJkxLk0vD0VSyrPRK63muS4lcWsPElNyM_6bgnwPGXjUpbqqiW_RDVLzgUEomckhoPqIm-BgDVqoLrtFhrxiog2C1VWMrdRCsRsFp7Ppnw7Bq0P4N_RpNwP0IYOq5cxhUNA5bg9aFpFJZ7_7f8AVM8JF7</recordid><startdate>202308</startdate><enddate>202308</enddate><creator>Kartal, Bahar</creator><creator>Alimoğulları, Ebru</creator><creator>Elçi, Pınar</creator><creator>Demir, Hazal</creator><general>Elsevier Ltd</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>7X8</scope><orcidid>https://orcid.org/0000-0001-9558-4122</orcidid></search><sort><creationdate>202308</creationdate><title>Adipose delivered stem cells protect liver after ischemia-reperfusion injury by controlling autophagy</title><author>Kartal, Bahar ; Alimoğulları, Ebru ; Elçi, Pınar ; Demir, Hazal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-27a06da77e03ca107ee98efe8d91e3c57c35a7c47c2ecf79fabaa64a97e27dc13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adipose Tissue</topic><topic>Adipose-derived stem cells(ADSCs)</topic><topic>Animals</topic><topic>Autophagy</topic><topic>Histopathology</topic><topic>Ischemia</topic><topic>Ischemia-reperfusion injury</topic><topic>Liver</topic><topic>Liver - pathology</topic><topic>Male</topic><topic>Rats</topic><topic>Reperfusion Injury - metabolism</topic><topic>Stem Cells - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kartal, Bahar</creatorcontrib><creatorcontrib>Alimoğulları, Ebru</creatorcontrib><creatorcontrib>Elçi, Pınar</creatorcontrib><creatorcontrib>Demir, Hazal</creatorcontrib><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>Injury</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kartal, Bahar</au><au>Alimoğulları, Ebru</au><au>Elçi, Pınar</au><au>Demir, Hazal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adipose delivered stem cells protect liver after ischemia-reperfusion injury by controlling autophagy</atitle><jtitle>Injury</jtitle><addtitle>Injury</addtitle><date>2023-08</date><risdate>2023</risdate><volume>54</volume><issue>8</issue><spage>110839</spage><epage>110839</epage><pages>110839-110839</pages><artnum>110839</artnum><issn>0020-1383</issn><eissn>1879-0267</eissn><abstract>: Ischemia-reperfusion(I/R) injury is an unavoidable side effect of liver surgery and transplantation. A potentially useful tool for cellular therapy and tissue engineering is adipose-derived stem cells (ADSCs).The process of autophagy is used by the cell to break down inappropriate molecules.The study's goal was to examine the impact of ADSCs on the autophagic pathway after rat hepatic ischemia-reperfusion injury.
: Thirty male rats used in our study were divided into control, ADSC, ischemia, I/R, and I/R+ ADSC groups (n = 6). Liver tissues were stained with hematoxylin-eosin and histological changes were evaluated with Suzuki scoring. Immunoexpressions of transforming growth factor (TGF-β) and autophagy markers LC3B, p62 were analyzed using the immunohistochemical method.
: As a result of histological evaluation the ischemia and I/R groups displayed sinusoid congestion, vacuolization, and necrosis in liver tissues. We showed that the immunostaining of LC3B and TGF- β were elevated, and p62 decreased in the rat liver from ischemia and I/R groups when compared to the control group.
: ADSCs reduced the excessive level of autophagy and structural damage to hepatocytes and the pathological alterations in the liver after ıschemia-reperfusion injury.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>37248113</pmid><doi>10.1016/j.injury.2023.110839</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9558-4122</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0020-1383 |
ispartof | Injury, 2023-08, Vol.54 (8), p.110839-110839, Article 110839 |
issn | 0020-1383 1879-0267 |
language | eng |
recordid | cdi_proquest_miscellaneous_2820971340 |
source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Adipose Tissue Adipose-derived stem cells(ADSCs) Animals Autophagy Histopathology Ischemia Ischemia-reperfusion injury Liver Liver - pathology Male Rats Reperfusion Injury - metabolism Stem Cells - metabolism |
title | Adipose delivered stem cells protect liver after ischemia-reperfusion injury by controlling autophagy |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T03%3A07%3A57IST&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=Adipose%20delivered%20stem%20cells%20protect%20liver%20after%20ischemia-reperfusion%20injury%20by%20controlling%20autophagy&rft.jtitle=Injury&rft.au=Kartal,%20Bahar&rft.date=2023-08&rft.volume=54&rft.issue=8&rft.spage=110839&rft.epage=110839&rft.pages=110839-110839&rft.artnum=110839&rft.issn=0020-1383&rft.eissn=1879-0267&rft_id=info:doi/10.1016/j.injury.2023.110839&rft_dat=%3Cproquest_cross%3E2820971340%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=2820971340&rft_id=info:pmid/37248113&rft_els_id=S0020138323005077&rfr_iscdi=true |