Mannowetz Nadja, Naidoo Natasha M, Choo Seung-A Sara, Smith James F, Lishko Polina V
Department of Molecular and Cell Biology , University of California, Berkeley , Berkeley , United States.
Elife. 2013 Oct 8;2:e01009. doi: 10.7554/eLife.01009.
Mammalian spermatozoa gain competence to fertilize an oocyte as they travel through the female reproductive tract. This process is accompanied by an elevation of sperm intracellular calcium and a membrane hyperpolarization. The latter is evoked by K(+) efflux; however, the molecular identity of the potassium channel of human spermatozoa (hKSper) is unknown. Here, we characterize hKSper, reporting that it is regulated by intracellular calcium but is insensitive to intracellular alkalinization. We also show that human KSper is inhibited by charybdotoxin, iberiotoxin, and paxilline, while mouse KSper is insensitive to these compounds. Such unique properties suggest that the Slo1 ion channel is the molecular determinant for hKSper. We show that Slo1 is localized to the sperm flagellum and is inhibited by progesterone. Inhibition of hKSper by progesterone may depolarize the spermatozoon to open the calcium channel CatSper, thus raising [Ca(2+)] to produce hyperactivation and allowing sperm to fertilize an oocyte. DOI:http://dx.doi.org/10.7554/eLife.01009.001.
哺乳动物的精子在穿过雌性生殖道的过程中获得使卵母细胞受精的能力。这一过程伴随着精子细胞内钙的升高和膜超极化。后者是由钾离子外流引起的;然而,人类精子钾通道(hKSper)的分子身份尚不清楚。在这里,我们对hKSper进行了表征,报告称它受细胞内钙的调节,但对细胞内碱化不敏感。我们还表明,人类KSper受到蝎毒素、iberiotoxin和鬼笔环肽的抑制,而小鼠KSper对这些化合物不敏感。这些独特的特性表明Slo1离子通道是hKSper的分子决定因素。我们表明Slo1定位于精子鞭毛,并受到孕酮的抑制。孕酮对hKSper的抑制可能会使精子去极化,从而打开钙通道CatSper,进而提高[Ca(2+)]以产生超激活,并使精子能够使卵母细胞受精。DOI:http://dx.doi.org/10.7554/eLife.01009.001 。