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Research shows non-muscle myosin II is crucial for cumulus cell migration during ovulation, indicating a complex pathway involving EGFR and Rho kinase.
At ovulation in mammals, epidermal growth factor (EGFR) signaling in the cumulus granulosa cells that enclose the egg causes them to generate an extracellular matrix and become dispersed within it. This process, termed expansion, is required for sperm to reach the egg. The extracellular signal-related kinase (ERK) pathway mediates matrix production, but the mechanism responsible for cell dispersion is poorly understood. We show that EGFR signaling activates non-muscle myosin II (NMII) in the cumulus cells and that NMII activity is required for full expansion. NMII activation does not require ERK signaling, but instead depends on the Rho-associated coiled-coil containing kinases (ROCK) and the myotonic dystrophy kinase-related CDC42-binding kinases (MRCK). Blocking ROCK or MRCK impairs the ability of the cumulus cells to migrate and reduces the number of sperm that penetrate through the cumulus layer to reach the oocyte. EGFR thus promotes cumulus layer expansion by integrating ERK-dependent production of the matrix with NMII-dependent migration of the cumulus cells within it. Activation by the epidermal growth factor receptor signaling pathway of non-muscle myosin II within the cumulus granulosa cells that surround the oocyte enables their migration away from it thereby facilitating sperm access and fertilization.
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Carvalho et al. (2025) studied this question.
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