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dc.contributor.authorCurley, Gerard F
dc.contributor.authorHayes, Mairead
dc.contributor.authorAnsari, Bilal
dc.contributor.authorShaw, Georgina
dc.contributor.authorRyan, Aideen
dc.contributor.authorBarry, Frank
dc.contributor.authorO'Brien, Timothy
dc.contributor.authorO'Toole, Daniel
dc.contributor.authorLaffey, John G
dc.date.accessioned2018-09-20T16:04:41Z
dc.date.available2018-09-20T16:04:41Z
dc.date.issued2011-11-21
dc.identifier.citationCurley, Gerard F; Hayes, Mairead; Ansari, Bilal; Shaw, Georgina; Ryan, Aideen; Barry, Frank; O'Brien, Timothy; O'Toole, Daniel; Laffey, John G (2011). Mesenchymal stem cells enhance recovery and repair following ventilator-induced lung injury in the rat. Thorax 67 (6), 496-501
dc.identifier.issn0040-6376,1468-3296
dc.identifier.urihttp://hdl.handle.net/10379/10997
dc.description.abstractBackground Bone-marrow derived mesenchymal stem cells (MSCs) reduce the severity of evolving acute lung injury (ALI), but their ability to repair the injured lung is not clear. A study was undertaken to determine the potential for MSCs to enhance repair after ventilator-induced lung injury (VILI) and elucidate the mechanisms underlying these effects. Methods Anaesthetised rats underwent injurious ventilation which produced severe ALI. Following recovery, they were given an intravenous injection of MSCs (2x10(6) cells) or vehicle immediately and a second dose 24 h later. The extent of recovery following VILI was assessed after 48 h. Subsequent experiments examined the potential for non-stem cells and for the MSC secretome to enhance VILI repair. The contribution of specific MSC-secreted mediators was then examined in a wound healing model. Results MSC therapy enhanced repair following VILI. MSCs enhanced restoration of systemic oxygenation and lung compliance, reduced total lung water, decreased lung inflammation and histological lung injury and restored lung structure. They attenuated alveolar tumour necrosis factor a concentrations while increasing concentrations of interleukin 10. These effects were not seen with non-stem cells (ie, rat fibroblasts). MSC-secreted products also enhanced lung repair and attenuated the inflammatory response following VILI. The beneficial effect of the MSC secretome on repair of pulmonary epithelial wounds was attenuated by prior depletion of keratinocyte growth factor. Conclusion MSC therapy enhances lung repair following VILI via a paracrine mechanism that may be keratinocyte growth factor-dependent.
dc.publisherBMJ
dc.relation.ispartofThorax
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectrespiratory-distress-syndrome
dc.subjectmarrow stromal cells
dc.subjecttidal volumes
dc.subjectmacrophages
dc.subjectmigration
dc.subjectresponses
dc.subjectstrategy
dc.subjectdelivery
dc.subjecttherapy
dc.subjecttissues
dc.titleMesenchymal stem cells enhance recovery and repair following ventilator-induced lung injury in the rat
dc.typeArticle
dc.identifier.doi10.1136/thoraxjnl-2011-201059
dc.local.publishedsourcehttps://thorax.bmj.com/content/67/6/496.full.pdf
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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland