Wang Bing, Cao Shu-Hua, Wang Yong-Qiang
Tianjin First Center Hospital, Tianjin 300192.
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2012 May;32(5):681-4.
To observe the effects of Modified Liangge Powder (MLP) on the expressions of platelet toll like receptor 4 (TLR4) and the release of platelet-derived cytokines interleukin 8 (IL-8), beta platelet globulin (beta-TG), soluble CD40 ligand (sCD40L).
The modulating effects on the release of cytokines from mice platelets by TLR4 ligand through monoclonal antibody blocking TLR4 on platelet were compared. The stimulated platelet by LPS was incubated with low (0.94 g/mL), medium (1.89 g/mL), and high (2.84 g/mL) dose of MLP contained serum. The changes of the platelet TLR4 expression and platelet-derived cytokines were observed.
The positive expression rate of platelet TLR4 obviously decreased (P < 0.01) and the release of sCD40L and beta-TG from platelets significantly increased (P < 0.01) after stimulated by LPS. However, the release of sCD40L and beta-TG from platelets obviously decreased by TLR4 monoclonal antibody (P < 0.05, P < 0.01). There was no statistical difference in IL-8 between before and after LPS stimulation (P > 0.05). Platelet TLR4 positive expression rate was significantly higher after incubated by medium and high doses of MLP contained serum (P < 0.01), and the releasing of sCD40L and beta-TG was lower in the serum contained groups. The inhibitory effects were enhanced in a dose-dependent manner.
LPS induced platelet activation by TLR4 and released sCD40L and beta-TG, while the release of platelet IL-8 was not dependent on platelet TLR4-LPS pathway. MLP could inhibit LPS-stimulated sCD40L and beta-TG, inhibit the binding of platelet TLR4 and LPS in a dose-dependent manner, thus reducing the release of platelet cytokines.
观察加味凉膈散对血小板Toll样受体4(TLR4)表达及血小板源性细胞因子白细胞介素8(IL-8)、β-血小板球蛋白(β-TG)、可溶性CD40配体(sCD40L)释放的影响。
通过单克隆抗体阻断血小板上的TLR4,比较TLR4配体对小鼠血小板细胞因子释放的调节作用。将脂多糖(LPS)刺激的血小板与含低(0.94 g/mL)、中(1.89 g/mL)、高(2.84 g/mL)剂量加味凉膈散的血清孵育,观察血小板TLR4表达及血小板源性细胞因子的变化。
LPS刺激后血小板TLR4阳性表达率明显降低(P<0.01),血小板sCD40L和β-TG释放明显增加(P<0.01)。然而,TLR4单克隆抗体可使血小板sCD40L和β-TG释放明显减少(P<0.05,P<0.01)。LPS刺激前后IL-8无统计学差异(P>0.05)。含中、高剂量加味凉膈散血清孵育后血小板TLR4阳性表达率明显升高(P<0.01),血清含药组sCD40L和β-TG释放较低,抑制作用呈剂量依赖性增强。
LPS通过TLR4诱导血小板活化并释放sCD40L和β-TG,而血小板IL-8的释放不依赖于血小板TLR4-LPS途径。加味凉膈散可抑制LPS刺激的sCD40L和β-TG,剂量依赖性抑制血小板TLR4与LPS的结合,从而减少血小板细胞因子的释放。