Jiang Weiwei, Ni Qingfeng, Tan Longwei, Kong Liangliang, Lu Yeting, Xu Xiaoqun, Kong Lianbao
Department of Neonatal Surgery, Nanjing Children's Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Liver Int. 2015 Mar;35(3):914-24. doi: 10.1111/liv.12674. Epub 2014 Sep 17.
BACKGROUND & AIMS: A critical role of the Toll-like receptor (TLR)-4 and its downstream mediators in the pathogenesis of small-for-size liver graft injury has been documented. Recently, the microRNA-146 (miR-146) was identified as a potent negative regulator of the TLR4 signalling pathway. In this study, the role of miR-146a and miR-146b in the attenuation of TLR-4 signalling and small-for-size liver graft injury was investigated.
The expression levels of miR-146a and miR-146b during small-for-size liver graft injury were studied in vivo. In addition, the effects of miR-146a and miR-146b on the expression of IRAK1 and TRAF6 in the rat macrophage cell line NR8383 and rat liver kupffer cells were studied in vitro. The in vivo effect of miR-146a and miR-146b on small-for-size liver graft injury was studied by the tail vein injection of miR-146a mimics and miR-146b mimics.
The levels of miR-146a and miR-146b decreased with a small-for-size liver graft. MiR-146a and miR-146b inhibited IRAK1 and TRAF6 expression by binding to the 3'UTR of IRAK1 or TRAF6, respectively, in the rat macrophage cell line NR8383. The administration of miR-146a mimics and miR-146b mimics prevented liver graft injury in small-for-size liver graft injury via the inactivation of IRAK1 and TRAF6 in vivo.
miR-146a and miR-146b prevent liver injury in small-for-size liver graft injury via the inactivation of IRAK1 and TRAF6.
Toll样受体(TLR)-4及其下游介质在小体积肝移植损伤发病机制中的关键作用已得到证实。最近,微小RNA-146(miR-146)被确定为TLR4信号通路的有效负调节因子。在本研究中,探讨了miR-146a和miR-146b在减弱TLR-4信号传导及小体积肝移植损伤中的作用。
在体内研究小体积肝移植损伤过程中miR-146a和miR-146b的表达水平。此外,在体外研究miR-146a和miR-146b对大鼠巨噬细胞系NR8383和大鼠肝库普弗细胞中IRAK1和TRAF6表达的影响。通过尾静脉注射miR-146a模拟物和miR-146b模拟物,在体内研究miR-146a和miR-146b对小体积肝移植损伤的影响。
小体积肝移植时,miR-146a和miR-146b水平降低。在大鼠巨噬细胞系NR8383中,miR-146a和miR-146b分别通过与IRAK1或TRAF6的3'非翻译区结合来抑制IRAK1和TRAF6的表达。在体内,给予miR-146a模拟物和miR-146b模拟物可通过使IRAK1和TRAF6失活来预防小体积肝移植损伤中的肝移植损伤。
miR-146a和miR-146b通过使IRAK1和TRAF6失活来预防小体积肝移植损伤中的肝损伤。