Zhu Xingxing, Shi Dongyan, Li Xiaoqian, Gong Weijuan, Wu Fengjiao, Guo Xuejiang, Xiao Hui, Liu Lixin, Zhou Hong
State Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 210029, China.
Department of Immunology, Nanjing Medical University, Nanjing 210029, China.
Cell Signal. 2016 Mar;28(3):148-156. doi: 10.1016/j.cellsig.2015.12.002. Epub 2015 Dec 4.
Infection in male and female genital tracts can lead to infertility. The underlying mechanisms of this process remain unclear. Toll-like receptors (TLRs) recognize conserved structures and respond to pathogens by initiating signals that activate inflammatory gene transcription. Here, we demonstrate that TLR activation in sperm reduces sperm motility via signalling through myeloid differentiation factor 88 (MyD88), phosphatidylinositol 3-kinase (PI3K), and glycogen synthase kinase (GSK)-3α. Upon TLR activation, phosphorylated forms of PI3K and GSK3α were detected in the mitochondria, and the mitochondrial membrane potential was impaired in sperm. In addition, mitochondrial ATP levels were decreased after TLR agonist stimulation. Furthermore, blocking PI3K or GSK3α activation abrogated these effects and reversed the TLR-induced reduction in sperm motility. These results identify a previously unrecognized TLR signalling pathway that leads to dysfunctional sperm mitochondria, which reduce sperm motility. Our study reveals a novel mechanism by which pathogenic infection affects sperm motility and possibly leads to infertility.
男性和女性生殖道感染可导致不孕。这一过程的潜在机制尚不清楚。Toll样受体(TLR)识别保守结构,并通过启动激活炎症基因转录的信号来应对病原体。在这里,我们证明精子中的TLR激活通过髓样分化因子88(MyD88)、磷脂酰肌醇3激酶(PI3K)和糖原合酶激酶(GSK)-3α发出信号,从而降低精子活力。TLR激活后,在精子线粒体中检测到PI3K和GSK3α的磷酸化形式,并且精子中的线粒体膜电位受损。此外,TLR激动剂刺激后线粒体ATP水平降低。此外,阻断PI3K或GSK3α的激活可消除这些影响,并逆转TLR诱导的精子活力降低。这些结果确定了一条以前未被认识的TLR信号通路,该通路导致精子线粒体功能失调,从而降低精子活力。我们的研究揭示了一种新机制,通过该机制病原体感染影响精子活力并可能导致不孕。