Polarized PtdIns(4,5)P<sub>2</sub> distribution mediated by a voltage-sensing phosphatase (VSP) regulates sperm motility.

Kawai, Takafumi; Miyata, Haruhiko; Nakanishi, Hiroki; Sakata, Souhei; Morioka, Shin; Sasaki, Junko; Watanabe, Masahiko; Sakimura, Kenji et al. · Proc Natl Acad Sci U S A · 2019

basic_science · Level V

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Abstract

The voltage-sensing phosphatase (VSP) is a unique protein that shows voltage-dependent phosphoinositide phosphatase activity. Here we report that VSP is activated in mice sperm flagellum and generates a unique subcellular distribution pattern of PtdIns(4,5)P<sub>2</sub> Sperm from VSP<sup>-/-</sup> mice show more Ca<sup>2+</sup> influx upon capacitation than VSP<sup>+/-</sup> mice and abnormal circular motion. VSP-deficient sperm showed enhanced activity of Slo3, a PtdIns(4,5)P<sub>2</sub>-sensitive K<sup>+</sup> channel, which selectively localizes to the principal piece of the flagellum and indirectly enhances Ca<sup>2+</sup> influx. Most interestingly, freeze-fracture electron microscopy analysis indicates that normal sperm have much less PtdIns(4,5)P<sub>2</sub> in the principal piece than in the midpiece of the flagellum, and this polarized PtdIns(4,5)P<sub>2</sub> distribution disappeared in VSP-deficient sperm. Thus, VSP appears to optimize PtdIns(4,5)P<sub>2</sub> distribution of the principal piece. These results imply that flagellar PtdIns(4,5)P<sub>2</sub> distribution plays important roles in ion channel regulation as well as sperm motility.

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