The direct electrophysiological characterization of sperm Ca 2ϩ channels has been precluded by their small size and flat shape. An alternative to study these channels is to use spermatogenic cells, the progenitors of sperm, which are larger and easier to patch-clamp. In mouse and rat, the only volta
Maitotoxin potently promotes Ca2+ influx in mouse spermatogenic cells and sperm, and induces the acrosome reaction
✍ Scribed by Claudia L. Treviño; José L. De la Vega-Beltrán; Takuya Nishigaki; Ricardo Felix; Alberto Darszon
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 266 KB
- Volume
- 206
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
Abstract
Maitotoxin (MTX), a potent marine toxin, activates Ca^2+^ entry via nonselective cation channels in a wide variety of cells. The identity of the channels involved in MTX action remains unknown. In mammalian sperm, Ca^2+^ entry through store‐operated channels regulates a number of physiological events including the acrosome reaction (AR). Here we report that MTX produced an increase in the intracellular concentration of Ca^2+^ ([Ca^2+^]~i~) in spermatogenic cells that depended on extracellular Ca^2+^. Ni^2+^ and SKF96365 diminished the MTX‐activated Ca^2+^ uptake, at concentrations they inhibit store‐operated channels, and in a similar manner as they inhibit the Ca^2+^ influx activated following depletion of intracellular stores by thapsigargin (Tpg). In addition, MTX significantly increased [Ca^2+^]~i~ in single mature sperm and effectively induced the AR with a half‐maximal concentration (ED~50~) of ∼1.1 nM. Notably, SKF96365 similarly inhibited the MTX‐induced increase in sperm [Ca^2+^]~i~ and the AR triggered by the toxin, Tpg and zona pellucida. These results suggest that putative MTX‐activated channels may be involved in the Ca^2+^ influx required for mouse sperm AR. J. Cell. Physiol. 206: 449–456, 2006. © 2005 Wiley‐Liss, Inc.
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