Laboratory of Animal Experiments for Regeneration, Institute for Frontier Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Development. 2014 May;141(10):2157-64. doi: 10.1242/dev.105148.
Mammalian sperm undergo multiple maturation steps after leaving the testis in order to become competent for fertilization, but the molecular mechanisms underlying this process remain unclear. In terms of identifying factors crucial for these processes in vivo, we found that lipocalin 2 (Lcn2), which is known as an innate immune factor inhibiting bacterial and malarial growth, can modulate sperm maturation. Most sperm that migrated to the oviduct of wild-type females underwent lipid raft reorganization and glycosylphosphatidylinositol-anchored protein shedding, which are signatures of sperm maturation, but few did so in Lcn2 null mice. Furthermore, we found that LCN2 binds to membrane phosphatidylethanolamine to reinforce lipid raft reorganization via a PKA-dependent mechanism and promotes sperm to acquire fertility by facilitating cholesterol efflux. These observations imply that mammals possess a mode for sperm maturation in addition to the albumin-mediated pathway.
哺乳动物精子离开睾丸后要经历多个成熟步骤才能具备受精能力,但这一过程的分子机制尚不清楚。在鉴定体内这些过程关键因素方面,我们发现,作为先天免疫因子抑制细菌和疟原虫生长的脂联素 2(Lcn2)可以调节精子成熟。大多数迁移到野生型雌性输卵管的精子经历脂质筏重排和糖基磷脂酰肌醇锚定蛋白脱落,这是精子成熟的特征,但在 Lcn2 缺失小鼠中很少发生。此外,我们发现 LCN2 与膜磷脂酰乙醇胺结合,通过 PKA 依赖性机制增强脂质筏重排,并通过促进胆固醇外排促进精子获得生育能力。这些观察结果表明,哺乳动物除了具有白蛋白介导的途径外,还具有一种精子成熟模式。