School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo 192-0392, Japan.
RIKEN Center for Developmental Biology, 2-2-3 Minatojima-Minamimachi, Chuo-ku, Kobe 650-0047, Japan.
J Biol Chem. 2014 Apr 18;289(16):11497-11511. doi: 10.1074/jbc.M113.531921. Epub 2014 Mar 5.
Recent studies have suggested that phosphatidic acid (PA), a cone-shaped phospholipid that can generate negative curvature of lipid membranes, participates in mitochondrial fusion. However, precise mechanisms underling the production and consumption of PA on the mitochondrial surface are not fully understood. Phosphatidic acid-preferring phospholipase A1 (PA-PLA1)/DDHD1 is the first identified intracellular phospholipase A1 and preferentially hydrolyzes PA in vitro. Its cellular and physiological functions have not been elucidated. In this study, we show that PA-PLA1 regulates mitochondrial dynamics. PA-PLA1, when ectopically expressed in HeLa cells, induced mitochondrial fragmentation, whereas its depletion caused mitochondrial elongation. The effects of PA-PLA1 on mitochondrial morphology appear to counteract those of MitoPLD, a mitochondrion-localized phospholipase D that produces PA from cardiolipin. Consistent with high levels of expression of PA-PLA1 in testis, PA-PLA1 knock-out mice have a defect in sperm formation. In PA-PLA1-deficient sperm, the mitochondrial structure is disorganized, and an abnormal gap structure exists between the middle and principal pieces. A flagellum is bent at that position, leading to a loss of motility. Our results suggest a possible mechanism of PA regulation of the mitochondrial membrane and demonstrate an in vivo function of PA-PLA1 in the organization of mitochondria during spermiogenesis.
最近的研究表明,磷脂酸(PA)是一种锥形磷脂,可以产生脂质膜的负曲率,参与线粒体融合。然而,PA 在线粒体表面的产生和消耗的确切机制尚不完全清楚。磷脂酸偏好性磷脂酶 A1(PA-PLA1)/DDHD1 是第一个被鉴定的细胞内磷脂酶 A1,它在体外优先水解 PA。其细胞和生理功能尚未阐明。在这项研究中,我们表明 PA-PLA1 调节线粒体动力学。PA-PLA1 在 HeLa 细胞中异位表达时,诱导线粒体碎片化,而其缺失则导致线粒体伸长。PA-PLA1 对线粒体形态的影响似乎与 MitoPLD 相反,后者是一种定位于线粒体的磷脂酶 D,可从心磷脂产生 PA。与 PA-PLA1 在睾丸中高表达一致,PA-PLA1 敲除小鼠的精子形成有缺陷。在 PA-PLA1 缺陷型精子中,线粒体结构紊乱,中主段之间存在异常的间隙结构。鞭毛在该位置弯曲,导致运动能力丧失。我们的结果表明了 PA 调节线粒体膜的一种可能机制,并证明了 PA-PLA1 在精子发生过程中线粒体组织中的体内功能。