Group of Skeletal, Mineral, and Gonadal Endocrinology, Department of Growth and Reproduction, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Division of Bone and Mineral Research, Harvard School of Dental Medicine/Harvard Medical School, Harvard University, Boston, MA, USA.
J Clin Endocrinol Metab. 2021 Mar 25;106(4):e1775-e1792. doi: 10.1210/clinem/dgaa937.
The calcium-sensing receptor (CaSR) is essential to maintain a stable calcium concentration in serum. Spermatozoa are exposed to immense changes in concentrations of CaSR ligands such as calcium, magnesium, and spermine during epididymal maturation, in the ejaculate, and in the female reproductive environment. However, the role of CaSR in human spermatozoa is unknown.
This work aimed to investigate the role of CaSR in human spermatozoa.
We identified CaSR in human spermatozoa and characterized the response to CaSR agonists on intracellular calcium, acrosome reaction, and 3',5'-cyclic adenosine 5'-monophosphate (cAMP) in spermatozoa from men with either loss-of-function or gain-of-function mutations in CASR and healthy donors.
CaSR is expressed in human spermatozoa and is essential for sensing extracellular free ionized calcium (Ca2+) and Mg2+. Activators of CaSR augmented the effect of sperm-activating signals such as the response to HCO3- and the acrosome reaction, whereas spermatozoa from men with a loss-of-function mutation in CASR had a diminished response to HCO3-, lower progesterone-mediated calcium influx, and were less likely to undergo the acrosome reaction in response to progesterone or Ca2+. CaSR activation increased cAMP through soluble adenylyl cyclase (sAC) activity and increased calcium influx through CatSper. Moreover, external Ca2+ or Mg2+ was indispensable for HCO3- activation of sAC. Two male patients with a CASR loss-of-function mutation in exon 3 presented with normal sperm counts and motility, whereas a patient with a loss-of-function mutation in exon 7 had low sperm count, motility, and morphology.
CaSR is important for the sensing of Ca2+, Mg2+, and HCO3- in spermatozoa, and loss-of-function may impair male sperm function.
钙敏感受体(CaSR)对于维持血清中钙离子的稳定浓度至关重要。在附睾成熟、精液中和女性生殖环境中,精子暴露于钙、镁和精胺等 CaSR 配体浓度的巨大变化中。然而,CaSR 在人类精子中的作用尚不清楚。
本研究旨在探讨 CaSR 在人类精子中的作用。
我们鉴定了人精子中的 CaSR,并对具有 CASR 功能丧失或功能获得突变的男性和健康供体的精子对 CaSR 激动剂的反应进行了细胞内钙离子、顶体反应和 3',5'-环磷酸腺苷(cAMP)的研究。
CaSR 表达于人精子中,对于感知细胞外游离钙离子(Ca2+)和镁离子(Mg2+)是必需的。CaSR 的激动剂增强了精子激活信号的作用,如对 HCO3-的反应和顶体反应,而 CASR 功能丧失突变的男性精子对 HCO3-的反应减弱,孕酮介导的钙内流减少,并且对孕酮或 Ca2+的顶体反应减少。CaSR 激活通过可溶性腺苷酸环化酶(sAC)活性增加 cAMP,并通过 CatSper 增加钙内流。此外,外部 Ca2+或 Mg2+对于 HCO3-激活 sAC 是必不可少的。两名具有外显子 3 功能丧失突变的男性患者的精子计数和活力正常,而具有外显子 7 功能丧失突变的患者的精子计数、活力和形态异常。
CaSR 对于精子中 Ca2+、Mg2+和 HCO3-的感知很重要,功能丧失可能会损害男性精子功能。