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Effects of various calcium transporters on mitochondrial Ca 2+ changes and oocyte maturation
Author(s) -
Wang Feng,
Fan LiHua,
Li Ang,
Dong Feng,
Hou Yi,
Schatten Heide,
Sun QingYuan,
Ou XiangHong
Publication year - 2021
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.30327
Subject(s) - germinal vesicle , oocyte , mibefradil , microbiology and biotechnology , oocyte activation , thapsigargin , in vitro maturation , calcium , chemistry , ruthenium red , mitochondrion , biology , voltage dependent calcium channel , intracellular , embryo , organic chemistry
Abstract Ca 2+ participates in many important cellular processes, but the underlying mechanisms are still poorly understood, especially during oocyte maturation. First, we confirmed that calcium in the culture medium was essential for oocyte maturation. Next, various inhibitors of Ca 2+ channels were applied to investigate their roles in mitochondrial Ca 2+ changes and oocyte maturation. Our results showed that Trmp7, Orai, T‐type Ca 2+ channels and Na + /Ca 2+ exchanger complex (NCLX) were important for oocyte maturation. Trmp7 inhibition delayed germinal vesicle breakdown. Orai and NCLX inhibition significantly weakened the distribution of mitochondrial Ca 2+ around the nucleus compared to the Ctrl group. Interestingly, even T‐type Ca 2+ channels‐specific inhibitor Mibefradil blocked germinal vesicle breakdown; mitochondrial Ca 2+ surrounding the nucleus still was maintained at a high level without spindle formation. Two calcium transporter inhibitors, Thapsigargin and Ruthenium Red, which have been confirmed to inhibit oocyte activation, did not significantly affect oocyte maturation. Increasing the knowledge of calcium transport may provide a basis to build on for improving oocyte in vitro maturation in human assisted reproduction clinics.