TLR4 Inhibits Mesenchymal Stem Cell MSC STAT3 Activation and Thereby Exerts Deleterious Effects on MSC–Mediated CardioprotectionReportar como inadecuado




TLR4 Inhibits Mesenchymal Stem Cell MSC STAT3 Activation and Thereby Exerts Deleterious Effects on MSC–Mediated Cardioprotection - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

Background

Bone marrow-derived mesenchymal stem cells MSC improve myocardial recovery after ischemia-reperfusion I-R injury. These effects are mediated in part by the paracrine secretion of angiogenic and tissue growth-promoting factors. Toll-like receptor 4 TLR4 is expressed by MSC and induces apoptosis and inhibits proliferation in neuronal progenitors as well as many other cell types. It is unknown whether knock-out KO of TLR4 will change the paracrine properties of MSC and in turn improve MSC-associated myocardial protection.

Methodology-Principal Findings

This study explored the effect of MSC TLR4 on the secretion of angiogenic factors and chemokines in vitro by using ELISA and cytokine array assays and investigated the role of TLR4 on MSC-mediated myocardial recovery after I-R injury in an isolated rat heart model. We observed that MSC isolated from TLR4 KO mice exhibited a greater degree of cardioprotection in a rat model of myocardial I-R injury. This enhanced protection was associated with increased angiogenic factor production, proliferation and differentiation. TLR4-dificiency was also associated with decreased phosphorylation of PI-3K and AKT, but increased activation of STAT3. siRNA targeting of STAT3 resulted in attenuation of the enhanced cardioprotection of TLR4-deficient MSC.

Conclusions-Significance

This study indicates that TLR4 exerts deleterious effects on MSC-derived cardioprotection following I-R by a STAT3 inhibitory mechanism.



Autor: Yue Wang , Aaron M. Abarbanell , Jeremy L. Herrmann, Brent R. Weil, Mariuxi C. Manukyan, Jeffrey A. Poynter, Daniel R. Meldrum

Fuente: http://plos.srce.hr/



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