Intravenous vs intraperitoneal mesenchymal stem cells administration: What is the best route for treating experimental colitis?
AIM:To investigate the therapeutic effects of mesenchymal stem cells(MSCs)transplanted intraperitoneally andintravenously in a murine model of colitis.METHODS:MSCs were isolated from C57BL/6 mouse adipose tissue.MSC cultures were analyzed according to morphology,cellular differentiation potential,an...
Gespeichert in:
Veröffentlicht in: | World journal of gastroenterology : WJG 2014-12, Vol.20 (48), p.18228-18239 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 18239 |
---|---|
container_issue | 48 |
container_start_page | 18228 |
container_title | World journal of gastroenterology : WJG |
container_volume | 20 |
creator | Gonçalves, Fabiany da Costa Schneider, Natália Pinto, Fernanda Otesbelgue Meyer, Fabíola Schons Visioli, Fernanda Pfaffenseller, Bianca Lopez, Patrícia Luciana da Costa Passos, Eduardo Pandolfi Cirne-Lima, Elizabeth Obino Meurer, Luíse Paz, Ana Helena |
description | AIM:To investigate the therapeutic effects of mesenchymal stem cells(MSCs)transplanted intraperitoneally andintravenously in a murine model of colitis.METHODS:MSCs were isolated from C57BL/6 mouse adipose tissue.MSC cultures were analyzed according to morphology,cellular differentiation potential,and surface molecular markers.Experimental acute colitis was induced in C57BL/6 mice by oral administration of2%dextran sulfate sodium(DSS)in drinking water ad libitum from days 0 to 7.Colitis mice were treated with1×106 MSCs via intraperitoneal or intravenous injection on days 2 and 5.The disease activity index was determined daily based on the following parameters:weight loss,stool consistency and presence of blood in the feces and anus.To compare morphological and functional differences in tissue regeneration between different MSC injection modalities,mice were euthanized on day 8,and their colons were examined for length,weight,and histopathological changes.Inflammatory responses were determined by measuring the levels of different serum cytokines using a CBA Th1/Th2/Th17 kit.Apoptotic rates were evaluated by terminal deoxynucleotidyl transferase-mediated d UDPbiotin nick end labeling assay.RESULTS:Intravenous infusion of MSCs was more effective than intraperitoneal treatment(P<0.001)in reducing the clinical and histopathologic severity of colitis,which includes weight loss,diarrhea and inflammation.An histological evaluation demonstrated decreased colonic inflammation based on reduced crypt loss and reduced infiltration of inflammatory cells.This therapeutic effect was most likely mediated by the down-regulation of pro-inflammatory cytokines[interleukin(IL)-6 and tumor necrosis factor(TNF)];and by the up-regulation of anti-inflammatory cytokines(IL-10 and IL-4).Intravenous transplantation alsoinduced high levels of IFN that lead to activation of the immunosuppressive activity of the MSCs,which did not occur with intraperitoneal transplantation(P=0.006).An increase in apoptotic T cells was observed after intravenous,but not intraperitoneal,MSC infusion,suggesting that MSCs can induce apoptosis in resistant T cells in colonic inflammation(P=0.027).CONCLUSION:Our results demonstrate that intravenous treatment is a superior method for reducing colon inflammation compared with intraperitoneal therapy. |
doi_str_mv | 10.3748/wjg.v20.i48.18228 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4277960</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>90888889504849525256484953</cqvip_id><sourcerecordid>1643145144</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-7cc7869c14c432e50ae730c13712730599943000651031bad7adc671f6ab36fe3</originalsourceid><addsrcrecordid>eNpVUU1v1DAUtBCIbgs_gAvykUuW54_EMQcQqqBUqsSlFUfL633ZuErsbexd6Im_jtMuq9Y-eCzPG783Q8g7BkuhZPvx9-1mueew9LJdspbz9gVZcM50xVsJL8mCAahKC65OyGlKtwBciJq_Jie8rhumNCzI38uQJ7vHEHeJ7hP183WLk88xoB3oiAmD6-_HglPGkTochkTtevTBp8LNPoZP9FdvM_WJ5h7pClOmU9xlpF2caJ6wkMKG4p9Zd8SQi5aLg88-fXlDXnV2SPj2cJ6Rm-_frs9_VFc_Ly7Pv15VTgLkSjmn2kY7Jp0UHGuwqAQ4JhTjBdRaaykAoKkZCLaya2XXrlGsa-xKNB2KM_L5UXe7W424djjPOZhtachO9yZab56_BN-bTdwbyZXSDRSBDweBKd7tyohm9Gk2wwYs3hnWSMFkzaQsVPZIdVNMacLu-A0DMwdnSnCmBGdKcOYhuFLz_ml_x4r_SRWCOIj2MWzuiqFHjoZ2XroG2Upd87KbByTEPyFeqD8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1643145144</pqid></control><display><type>article</type><title>Intravenous vs intraperitoneal mesenchymal stem cells administration: What is the best route for treating experimental colitis?</title><source>MEDLINE</source><source>Baishideng "World Journal of" online journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Gonçalves, Fabiany da Costa ; Schneider, Natália ; Pinto, Fernanda Otesbelgue ; Meyer, Fabíola Schons ; Visioli, Fernanda ; Pfaffenseller, Bianca ; Lopez, Patrícia Luciana da Costa ; Passos, Eduardo Pandolfi ; Cirne-Lima, Elizabeth Obino ; Meurer, Luíse ; Paz, Ana Helena</creator><creatorcontrib>Gonçalves, Fabiany da Costa ; Schneider, Natália ; Pinto, Fernanda Otesbelgue ; Meyer, Fabíola Schons ; Visioli, Fernanda ; Pfaffenseller, Bianca ; Lopez, Patrícia Luciana da Costa ; Passos, Eduardo Pandolfi ; Cirne-Lima, Elizabeth Obino ; Meurer, Luíse ; Paz, Ana Helena</creatorcontrib><description>AIM:To investigate the therapeutic effects of mesenchymal stem cells(MSCs)transplanted intraperitoneally andintravenously in a murine model of colitis.METHODS:MSCs were isolated from C57BL/6 mouse adipose tissue.MSC cultures were analyzed according to morphology,cellular differentiation potential,and surface molecular markers.Experimental acute colitis was induced in C57BL/6 mice by oral administration of2%dextran sulfate sodium(DSS)in drinking water ad libitum from days 0 to 7.Colitis mice were treated with1×106 MSCs via intraperitoneal or intravenous injection on days 2 and 5.The disease activity index was determined daily based on the following parameters:weight loss,stool consistency and presence of blood in the feces and anus.To compare morphological and functional differences in tissue regeneration between different MSC injection modalities,mice were euthanized on day 8,and their colons were examined for length,weight,and histopathological changes.Inflammatory responses were determined by measuring the levels of different serum cytokines using a CBA Th1/Th2/Th17 kit.Apoptotic rates were evaluated by terminal deoxynucleotidyl transferase-mediated d UDPbiotin nick end labeling assay.RESULTS:Intravenous infusion of MSCs was more effective than intraperitoneal treatment(P&lt;0.001)in reducing the clinical and histopathologic severity of colitis,which includes weight loss,diarrhea and inflammation.An histological evaluation demonstrated decreased colonic inflammation based on reduced crypt loss and reduced infiltration of inflammatory cells.This therapeutic effect was most likely mediated by the down-regulation of pro-inflammatory cytokines[interleukin(IL)-6 and tumor necrosis factor(TNF)];and by the up-regulation of anti-inflammatory cytokines(IL-10 and IL-4).Intravenous transplantation alsoinduced high levels of IFN that lead to activation of the immunosuppressive activity of the MSCs,which did not occur with intraperitoneal transplantation(P=0.006).An increase in apoptotic T cells was observed after intravenous,but not intraperitoneal,MSC infusion,suggesting that MSCs can induce apoptosis in resistant T cells in colonic inflammation(P=0.027).CONCLUSION:Our results demonstrate that intravenous treatment is a superior method for reducing colon inflammation compared with intraperitoneal therapy.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v20.i48.18228</identifier><identifier>PMID: 25561790</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Inc</publisher><subject>Acute Disease ; Animals ; Apoptosis ; Biomarkers - blood ; Cells, Cultured ; colitis ; Colitis - blood ; Colitis - chemically induced ; Colitis - pathology ; Colitis - physiopathology ; Colitis - surgery ; Colon - metabolism ; Colon - pathology ; Colon - physiopathology ; Cytokines - blood ; Dextran ; Dextran Sulfate ; Disease Models, Animal ; Inflamma ; Inflammation Mediators - blood ; Infusions, Intravenous ; Infusions, Parenteral ; Male ; Mesenchymal Stem Cell Transplantation - methods ; Mesenchymal Stromal Cells - metabolism ; Mice, Inbred C57BL ; Original ; Phenotype ; Regeneration ; sodium ; sulfate ; T-Lymphocytes - metabolism ; T-Lymphocytes - pathology ; Time Factors ; Ulcerative</subject><ispartof>World journal of gastroenterology : WJG, 2014-12, Vol.20 (48), p.18228-18239</ispartof><rights>2014 Baishideng Publishing Group Inc. All rights reserved. 2014</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-7cc7869c14c432e50ae730c13712730599943000651031bad7adc671f6ab36fe3</citedby><cites>FETCH-LOGICAL-c400t-7cc7869c14c432e50ae730c13712730599943000651031bad7adc671f6ab36fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4277960/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4277960/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25561790$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gonçalves, Fabiany da Costa</creatorcontrib><creatorcontrib>Schneider, Natália</creatorcontrib><creatorcontrib>Pinto, Fernanda Otesbelgue</creatorcontrib><creatorcontrib>Meyer, Fabíola Schons</creatorcontrib><creatorcontrib>Visioli, Fernanda</creatorcontrib><creatorcontrib>Pfaffenseller, Bianca</creatorcontrib><creatorcontrib>Lopez, Patrícia Luciana da Costa</creatorcontrib><creatorcontrib>Passos, Eduardo Pandolfi</creatorcontrib><creatorcontrib>Cirne-Lima, Elizabeth Obino</creatorcontrib><creatorcontrib>Meurer, Luíse</creatorcontrib><creatorcontrib>Paz, Ana Helena</creatorcontrib><title>Intravenous vs intraperitoneal mesenchymal stem cells administration: What is the best route for treating experimental colitis?</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM:To investigate the therapeutic effects of mesenchymal stem cells(MSCs)transplanted intraperitoneally andintravenously in a murine model of colitis.METHODS:MSCs were isolated from C57BL/6 mouse adipose tissue.MSC cultures were analyzed according to morphology,cellular differentiation potential,and surface molecular markers.Experimental acute colitis was induced in C57BL/6 mice by oral administration of2%dextran sulfate sodium(DSS)in drinking water ad libitum from days 0 to 7.Colitis mice were treated with1×106 MSCs via intraperitoneal or intravenous injection on days 2 and 5.The disease activity index was determined daily based on the following parameters:weight loss,stool consistency and presence of blood in the feces and anus.To compare morphological and functional differences in tissue regeneration between different MSC injection modalities,mice were euthanized on day 8,and their colons were examined for length,weight,and histopathological changes.Inflammatory responses were determined by measuring the levels of different serum cytokines using a CBA Th1/Th2/Th17 kit.Apoptotic rates were evaluated by terminal deoxynucleotidyl transferase-mediated d UDPbiotin nick end labeling assay.RESULTS:Intravenous infusion of MSCs was more effective than intraperitoneal treatment(P&lt;0.001)in reducing the clinical and histopathologic severity of colitis,which includes weight loss,diarrhea and inflammation.An histological evaluation demonstrated decreased colonic inflammation based on reduced crypt loss and reduced infiltration of inflammatory cells.This therapeutic effect was most likely mediated by the down-regulation of pro-inflammatory cytokines[interleukin(IL)-6 and tumor necrosis factor(TNF)];and by the up-regulation of anti-inflammatory cytokines(IL-10 and IL-4).Intravenous transplantation alsoinduced high levels of IFN that lead to activation of the immunosuppressive activity of the MSCs,which did not occur with intraperitoneal transplantation(P=0.006).An increase in apoptotic T cells was observed after intravenous,but not intraperitoneal,MSC infusion,suggesting that MSCs can induce apoptosis in resistant T cells in colonic inflammation(P=0.027).CONCLUSION:Our results demonstrate that intravenous treatment is a superior method for reducing colon inflammation compared with intraperitoneal therapy.</description><subject>Acute Disease</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Biomarkers - blood</subject><subject>Cells, Cultured</subject><subject>colitis</subject><subject>Colitis - blood</subject><subject>Colitis - chemically induced</subject><subject>Colitis - pathology</subject><subject>Colitis - physiopathology</subject><subject>Colitis - surgery</subject><subject>Colon - metabolism</subject><subject>Colon - pathology</subject><subject>Colon - physiopathology</subject><subject>Cytokines - blood</subject><subject>Dextran</subject><subject>Dextran Sulfate</subject><subject>Disease Models, Animal</subject><subject>Inflamma</subject><subject>Inflammation Mediators - blood</subject><subject>Infusions, Intravenous</subject><subject>Infusions, Parenteral</subject><subject>Male</subject><subject>Mesenchymal Stem Cell Transplantation - methods</subject><subject>Mesenchymal Stromal Cells - metabolism</subject><subject>Mice, Inbred C57BL</subject><subject>Original</subject><subject>Phenotype</subject><subject>Regeneration</subject><subject>sodium</subject><subject>sulfate</subject><subject>T-Lymphocytes - metabolism</subject><subject>T-Lymphocytes - pathology</subject><subject>Time Factors</subject><subject>Ulcerative</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1v1DAUtBCIbgs_gAvykUuW54_EMQcQqqBUqsSlFUfL633ZuErsbexd6Im_jtMuq9Y-eCzPG783Q8g7BkuhZPvx9-1mueew9LJdspbz9gVZcM50xVsJL8mCAahKC65OyGlKtwBciJq_Jie8rhumNCzI38uQJ7vHEHeJ7hP183WLk88xoB3oiAmD6-_HglPGkTochkTtevTBp8LNPoZP9FdvM_WJ5h7pClOmU9xlpF2caJ6wkMKG4p9Zd8SQi5aLg88-fXlDXnV2SPj2cJ6Rm-_frs9_VFc_Ly7Pv15VTgLkSjmn2kY7Jp0UHGuwqAQ4JhTjBdRaaykAoKkZCLaya2XXrlGsa-xKNB2KM_L5UXe7W424djjPOZhtachO9yZab56_BN-bTdwbyZXSDRSBDweBKd7tyohm9Gk2wwYs3hnWSMFkzaQsVPZIdVNMacLu-A0DMwdnSnCmBGdKcOYhuFLz_ml_x4r_SRWCOIj2MWzuiqFHjoZ2XroG2Upd87KbByTEPyFeqD8</recordid><startdate>20141228</startdate><enddate>20141228</enddate><creator>Gonçalves, Fabiany da Costa</creator><creator>Schneider, Natália</creator><creator>Pinto, Fernanda Otesbelgue</creator><creator>Meyer, Fabíola Schons</creator><creator>Visioli, Fernanda</creator><creator>Pfaffenseller, Bianca</creator><creator>Lopez, Patrícia Luciana da Costa</creator><creator>Passos, Eduardo Pandolfi</creator><creator>Cirne-Lima, Elizabeth Obino</creator><creator>Meurer, Luíse</creator><creator>Paz, Ana Helena</creator><general>Baishideng Publishing Group Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><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><scope>5PM</scope></search><sort><creationdate>20141228</creationdate><title>Intravenous vs intraperitoneal mesenchymal stem cells administration: What is the best route for treating experimental colitis?</title><author>Gonçalves, Fabiany da Costa ; Schneider, Natália ; Pinto, Fernanda Otesbelgue ; Meyer, Fabíola Schons ; Visioli, Fernanda ; Pfaffenseller, Bianca ; Lopez, Patrícia Luciana da Costa ; Passos, Eduardo Pandolfi ; Cirne-Lima, Elizabeth Obino ; Meurer, Luíse ; Paz, Ana Helena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-7cc7869c14c432e50ae730c13712730599943000651031bad7adc671f6ab36fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acute Disease</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Biomarkers - blood</topic><topic>Cells, Cultured</topic><topic>colitis</topic><topic>Colitis - blood</topic><topic>Colitis - chemically induced</topic><topic>Colitis - pathology</topic><topic>Colitis - physiopathology</topic><topic>Colitis - surgery</topic><topic>Colon - metabolism</topic><topic>Colon - pathology</topic><topic>Colon - physiopathology</topic><topic>Cytokines - blood</topic><topic>Dextran</topic><topic>Dextran Sulfate</topic><topic>Disease Models, Animal</topic><topic>Inflamma</topic><topic>Inflammation Mediators - blood</topic><topic>Infusions, Intravenous</topic><topic>Infusions, Parenteral</topic><topic>Male</topic><topic>Mesenchymal Stem Cell Transplantation - methods</topic><topic>Mesenchymal Stromal Cells - metabolism</topic><topic>Mice, Inbred C57BL</topic><topic>Original</topic><topic>Phenotype</topic><topic>Regeneration</topic><topic>sodium</topic><topic>sulfate</topic><topic>T-Lymphocytes - metabolism</topic><topic>T-Lymphocytes - pathology</topic><topic>Time Factors</topic><topic>Ulcerative</topic><toplevel>online_resources</toplevel><creatorcontrib>Gonçalves, Fabiany da Costa</creatorcontrib><creatorcontrib>Schneider, Natália</creatorcontrib><creatorcontrib>Pinto, Fernanda Otesbelgue</creatorcontrib><creatorcontrib>Meyer, Fabíola Schons</creatorcontrib><creatorcontrib>Visioli, Fernanda</creatorcontrib><creatorcontrib>Pfaffenseller, Bianca</creatorcontrib><creatorcontrib>Lopez, Patrícia Luciana da Costa</creatorcontrib><creatorcontrib>Passos, Eduardo Pandolfi</creatorcontrib><creatorcontrib>Cirne-Lima, Elizabeth Obino</creatorcontrib><creatorcontrib>Meurer, Luíse</creatorcontrib><creatorcontrib>Paz, Ana Helena</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gonçalves, Fabiany da Costa</au><au>Schneider, Natália</au><au>Pinto, Fernanda Otesbelgue</au><au>Meyer, Fabíola Schons</au><au>Visioli, Fernanda</au><au>Pfaffenseller, Bianca</au><au>Lopez, Patrícia Luciana da Costa</au><au>Passos, Eduardo Pandolfi</au><au>Cirne-Lima, Elizabeth Obino</au><au>Meurer, Luíse</au><au>Paz, Ana Helena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intravenous vs intraperitoneal mesenchymal stem cells administration: What is the best route for treating experimental colitis?</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2014-12-28</date><risdate>2014</risdate><volume>20</volume><issue>48</issue><spage>18228</spage><epage>18239</epage><pages>18228-18239</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>AIM:To investigate the therapeutic effects of mesenchymal stem cells(MSCs)transplanted intraperitoneally andintravenously in a murine model of colitis.METHODS:MSCs were isolated from C57BL/6 mouse adipose tissue.MSC cultures were analyzed according to morphology,cellular differentiation potential,and surface molecular markers.Experimental acute colitis was induced in C57BL/6 mice by oral administration of2%dextran sulfate sodium(DSS)in drinking water ad libitum from days 0 to 7.Colitis mice were treated with1×106 MSCs via intraperitoneal or intravenous injection on days 2 and 5.The disease activity index was determined daily based on the following parameters:weight loss,stool consistency and presence of blood in the feces and anus.To compare morphological and functional differences in tissue regeneration between different MSC injection modalities,mice were euthanized on day 8,and their colons were examined for length,weight,and histopathological changes.Inflammatory responses were determined by measuring the levels of different serum cytokines using a CBA Th1/Th2/Th17 kit.Apoptotic rates were evaluated by terminal deoxynucleotidyl transferase-mediated d UDPbiotin nick end labeling assay.RESULTS:Intravenous infusion of MSCs was more effective than intraperitoneal treatment(P&lt;0.001)in reducing the clinical and histopathologic severity of colitis,which includes weight loss,diarrhea and inflammation.An histological evaluation demonstrated decreased colonic inflammation based on reduced crypt loss and reduced infiltration of inflammatory cells.This therapeutic effect was most likely mediated by the down-regulation of pro-inflammatory cytokines[interleukin(IL)-6 and tumor necrosis factor(TNF)];and by the up-regulation of anti-inflammatory cytokines(IL-10 and IL-4).Intravenous transplantation alsoinduced high levels of IFN that lead to activation of the immunosuppressive activity of the MSCs,which did not occur with intraperitoneal transplantation(P=0.006).An increase in apoptotic T cells was observed after intravenous,but not intraperitoneal,MSC infusion,suggesting that MSCs can induce apoptosis in resistant T cells in colonic inflammation(P=0.027).CONCLUSION:Our results demonstrate that intravenous treatment is a superior method for reducing colon inflammation compared with intraperitoneal therapy.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Inc</pub><pmid>25561790</pmid><doi>10.3748/wjg.v20.i48.18228</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1007-9327 |
ispartof | World journal of gastroenterology : WJG, 2014-12, Vol.20 (48), p.18228-18239 |
issn | 1007-9327 2219-2840 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4277960 |
source | MEDLINE; Baishideng "World Journal of" online journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
subjects | Acute Disease Animals Apoptosis Biomarkers - blood Cells, Cultured colitis Colitis - blood Colitis - chemically induced Colitis - pathology Colitis - physiopathology Colitis - surgery Colon - metabolism Colon - pathology Colon - physiopathology Cytokines - blood Dextran Dextran Sulfate Disease Models, Animal Inflamma Inflammation Mediators - blood Infusions, Intravenous Infusions, Parenteral Male Mesenchymal Stem Cell Transplantation - methods Mesenchymal Stromal Cells - metabolism Mice, Inbred C57BL Original Phenotype Regeneration sodium sulfate T-Lymphocytes - metabolism T-Lymphocytes - pathology Time Factors Ulcerative |
title | Intravenous vs intraperitoneal mesenchymal stem cells administration: What is the best route for treating experimental colitis? |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T02%3A06%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intravenous%20vs%20intraperitoneal%20mesenchymal%20stem%20cells%20administration:%20What%20is%20the%20best%20route%20for%20treating%20experimental%20colitis?&rft.jtitle=World%20journal%20of%20gastroenterology%20:%20WJG&rft.au=Gon%C3%A7alves,%20Fabiany%20da%20Costa&rft.date=2014-12-28&rft.volume=20&rft.issue=48&rft.spage=18228&rft.epage=18239&rft.pages=18228-18239&rft.issn=1007-9327&rft.eissn=2219-2840&rft_id=info:doi/10.3748/wjg.v20.i48.18228&rft_dat=%3Cproquest_pubme%3E1643145144%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1643145144&rft_id=info:pmid/25561790&rft_cqvip_id=90888889504849525256484953&rfr_iscdi=true |