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dc.contributor.authorHuang, Xiaojia
dc.contributor.authorZhao, You-Yang
dc.date.accessioned2013-11-26T20:37:51Z
dc.date.available2013-11-26T20:37:51Z
dc.date.issued2012-11
dc.identifier.bibliographicCitationHuang X, Zhao Y-Y (2012) Transgenic Expression of FoxM1 Promotes Endothelial Repair following Lung Injury Induced by Polymicrobial Sepsis in Mice. PLoS ONE 7(11): e50094. doi:10.1371/journal.pone.0050094en_US
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10027/10668
dc.description© Huang, Zhao. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. The original version is available through Public Library of Science at DOI: 10.1371/journal.pone.0050094.en_US
dc.description.abstractEnhancing endothelial barrier integrity for the treatment of acute lung injury (ALI) is an emerging novel therapeutic strategy. Our previous studies have demonstrated the essential role of FoxM1 in mediating endothelial regeneration and barrier repair following lipopolysaccharide-induced lung injury. However, it remains unclear whether FoxM1 expression is sufficient to promote endothelial repair in experimental models of sepsis. Here, employing the FoxM1 transgenic (FoxM1 Tg) mice, we showed that transgenic expression of FoxM1 promoted rapid recovery of endothelial barrier function and survival in a clinically relevant model of sepsis induced by cecal ligation and puncture (CLP). We observed lung vascular permeability was rapidly recovered and returned to levels similar to baseline at 48 h post-CLP challenge in FoxM1 Tg mice whereas it remained markedly elevated in WT mice. Lung edema and inflammation were resolved only in FoxM1 Tg mice at 24 h post- CLP. 5-bromo-2-deoxyuridine incorporation assay revealed a drastic induction of endothelial proliferation in FoxM1 Tg lungs at 24h post-CLP, correlating with early induction of expression of FoxM1 target genes essential for cell cycle progression. Additionally, deletion of FoxM1 in endothelial cells, employing the mouse model with endothelial cell-restricted disruption of FoxM1 (FoxM1 CKO) resulted in impaired endothelial repair following CLP challenge. Together, these data suggest FoxM1 expression in endothelial cells is necessary and sufficient to mediate endothelial repair and thereby promote survival following sepsis challenge.en_US
dc.description.sponsorshipThis study was supported by National Institutes of Health grants R01HL085462 and P01HL077806 to YYZ.en_US
dc.language.isoen_USen_US
dc.publisherPublic Library of Scienceen_US
dc.titleTransgenic Expression of FoxM1 Promotes Endothelial Repair following Lung Injury Induced by Polymicrobial Sepsis in Miceen_US
dc.typeArticleen_US


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