Lysophosphatidic Acid Improves Human Sperm Motility by Enhancing Glycolysis and Activating L-Type Calcium Channels

被引:12
|
作者
Li, Yinlam [1 ,2 ]
Jin, Li [3 ]
Li, Yanquan [1 ,2 ]
Qian, Jianing [4 ]
Wang, Zhengquan [1 ]
Zheng, Xiaoguo [1 ,2 ]
Xie, Chong [1 ]
Zhang, Xuelian [4 ]
Huang, Hefeng [1 ,2 ]
Zhou, Yuchuan [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Int Peace Matern & Child Hlth Hosp, Sch Med, Shanghai, Peoples R China
[2] Shanghai Key Lab Embryo Original Dis, Shanghai, Peoples R China
[3] Fudan Univ, Obstet & Gynecol Hosp, Inst Reprod & Dev, Shanghai, Peoples R China
[4] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai, Peoples R China
来源
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
lysophosphatidic acid; human spermatozoa; sperm motility; glycolysis; LPA receptors; calcium channels; IN-VITRO FERTILIZATION; PHOSPHODIESTERASE INHIBITORS; MOUSE; RECEPTOR; CAPACITATION; MATURATION; PROTEIN; SPERMATOZOA; METABOLISM; OOCYTES;
D O I
10.3389/fendo.2022.896558
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Until now, the molecular mechanisms underlining sperm motility defect causing male infertility are still poorly understood. Safe and effective compounds or drugs that can improve sperm motility are also very limited. Lysophosphatidic acid (LPA) is a naturally occurring phospholipid and a bioactive intermediate with multiple biological activities. It has been detected in various body fluids such as serum, plasma, saliva, tears, blister fluids, hen egg white, and ascites from patients with ovarian cancer. LPA is also abundant in seminal plasma and follicular fluid. It enhances follicle stimulation, improves oocyte fertilization, and promotes early embryonic development and embryo implantation. However, the physiological role of LPA in the male reproductive system remains unknown. Here, our study showed that LPA significantly improved the motility parameters of human sperm hyperactivation in a dose-dependent manner. The LPA-induced elevation of sperm motility is dependent on bovine serum albumin (BSA) but independent of the classical BSA-induced sAC/cAMP/PKA signaling pathway. The enhancement of sperm motility by LPA could not be blocked by CCCP, a respiratory inhibitor suppressing mitochondrial ATP production. Moreover, LPA improved the activity of triosephosphate isomerase in glycolysis. Meanwhile, LPA treatment significantly increased ATP and phosphoenolpyruvate levels and decreased ADP content during sperm glycolysis. Notably, none of known or identified LPA receptors was detected in human sperm. Further investigations showed that LPA promoted sperm motility through L-type calcium channels. In summary, this study revealed the involvement of LPA in the regulation for human sperm motility by enhancing glycolysis and activating L-type calcium channels. The current findings may shed new light on the understanding of causes of asthenozoospermia, and indicate that LPA could be used as a novel therapeutic agent to improve sperm function and fertilizing capacity.
引用
收藏
页数:12
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