The actin polymerization regulator Thymosin ?4 (T?4) has been shown to be involved in angiogenesis, wound healing, cell survival and anti-inflammatory responses. We have previously shown that T?4 is capable of recruiting pericytes, thus stabilizing the endothelial barrier function. Here, we analyzed whether treatment with T?4 is able to reduce the pericytes loss in lipopolysaccharides (LPS)-induced sepsis and to improve the hemodynamic function and survival in C57BL/6 mice.Fourteen days before LPS injection, the mice were injected with an adeno-associated virus carrying the T?4 (rAAV.T?4) or LacZ gene (rAAV.LacZ). A sepsis-severity score was assessed, and non-invasive hemodynamic and permeability measurements were performed. Heart and muscle samples were analyzed for PECAM-1(+) capillaries and NG2(+)pericytes.At 36 h, there was a decrease of sepsis severity score in rAAV.T?4-treated animals as compared to rAAV.LacZ-treated control. rAAV.T?4-treated animals displayed lower perivascular leakage and higher blood pressure compared to control. Of note, the rAAV.T?4 group showed a higher pericyte count in heart and peripheral muscle samples. Finally, T?4-treatment reduced mortality compared to control.The data indicate a preventive role of T?4 in septic hypercirculation and highlight T?4 as a potential therapeutic target in severe sepsis.     «

The actin polymerization regulator Thymosin ?4 (T?4) has been shown to be involved in angiogenesis, wound healing, cell survival and anti-inflammatory responses. We have previously shown that T?4 is capable of recruiting pericytes, thus stabilizing the endothelial barrier function. Here, we analyzed whether treatment with T?4 is able to reduce the pericytes loss in lipopolysaccharides (LPS)-induced sepsis and to improve the hemodynamic function and survival in C57BL/6 mice.Fourteen days before L...     »