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dc.contributor.authorMilwid, John Miles
dc.contributor.authorIchimura, Takaharu
dc.contributor.authorLi, Matthew
dc.contributor.authorJiao, Yunxin
dc.contributor.authorLee, Jungwoo
dc.contributor.authorYarmush, Joshua S.
dc.contributor.authorParekkadan, Biju
dc.contributor.authorTilles, Arno W.
dc.contributor.authorBonventre, Joseph V.
dc.contributor.authorYarmush, Martin L.
dc.date.accessioned2013-06-13T19:30:10Z
dc.date.available2013-06-13T19:30:10Z
dc.date.issued2012
dc.date.submitted2012-09
dc.identifier.issn1687-966X
dc.identifier.issn1687-9678
dc.identifier.urihttp://hdl.handle.net/1721.1/79100
dc.description.abstractAcute kidney injury is a devastating syndrome that afflicts over 2,000,000 people in the US per year, with an associated mortality of greater than 70% in severe cases. Unfortunately, standard-of-care treatments are not sufficient for modifying the course of disease. Many groups have explored the use of bone marrow stromal cells (BMSCs) for the treatment of AKI because BMSCs have been shown to possess unique anti-inflammatory, cytoprotective, and regenerative properties in vitro and in vivo. It is yet unresolved whether the primary mechanisms controlling BMSC therapy in AKI depend on direct cell infusion, or whether BMSC-secreted factors alone are sufficient for mitigating the injury. Here we show that BMSC-secreted factors are capable of providing a survival benefit to rats subjected to cisplatin-induced AKI. We observed that when BMSC-conditioned medium (BMSC-CM) is administered intravenously, it prevents tubular apoptosis and necrosis and ameliorates AKI. In addition, we observed that BMSC-CM causes IL-10 upregulation in treated animals, which is important to animal survival and protection of the kidney. In all, these results demonstrate that BMSC-secreted factors are capable of providing support without cell transplantation, and the IL-10 increase seen in BMSC-CM-treated animals correlates with attenuation of severe AKI.en_US
dc.description.sponsorshipNational Human Genome Research Institute (U.S.) (Grant number T32 HG002295)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant K01DK087770)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R21DK085267)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant DK39773)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant DK72381)en_US
dc.description.sponsorshipShriners Hospitals for Childrenen_US
dc.publisherHindawi Publishing Corporationen_US
dc.relation.isversionofhttp://dx.doi.org/10.1155/2012/392050en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceHindawi Publishing Corporationen_US
dc.titleSecreted Factors from Bone Marrow Stromal Cells Upregulate IL-10 and Reverse Acute Kidney Injuryen_US
dc.typeArticleen_US
dc.identifier.citationMilwid, Jack M. et al. "Secreted Factors from Bone Marrow Stromal Cells Upregulate IL-10 and Reverse Acute Kidney Injury." Stem Cells International, Volume 2012 (2012), Article ID 392050, 12 pages.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorMilwid, John Milesen_US
dc.contributor.mitauthorBonventre, Joseph V.en_US
dc.relation.journalStem Cells Internationalen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2013-05-28T11:44:29Z
dc.language.rfc3066en
dc.rights.holderCopyright © 2012 Jack M. Milwid et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dspace.orderedauthorsMilwid, Jack M.; Ichimura, Takaharu; Li, Matthew; Jiao, Yunxin; Lee, Jungwoo; Yarmush, Joshua S.; Parekkadan, Biju; Tilles, Arno W.; Bonventre, Joseph V.; Yarmush, Martin L.en_US
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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