Emi Kuwahara1, Junpei Yamamoto1, Yuya Yano2, Midori Omura1, Akira Kuwahara2, Minoru Irahara2, Akira Tokumura1. 1. Department of Pharmaceutical Health Chemistry, Institute of Health Biosciences University of Tokushima Graduate School Shomachi 770-8505 Tokushima Japan. 2. Department of Obstetrics and Gynecology, School of Medicine, Institute of Health Biosciences University of Tokushima Kuramoto-cho 770-8503 Tokushima Japan.
Abstract
Purpose: In mammals, cumulus expansion due to increased synthesis of hyaluronan was suggested to correlate with modification of the gap junction between cumulus cells and the oocyte, leading to cumulus expansion. We examined whether lysophosphatidic acid, a lipid mediator detected in mammalian body fluids, stimulates significant production of hyaluronan and thus affects mouse cumulus expansion in vitro. Methods: Cumulus-oocyte complexes isolated from the gonadotropin-treated ovaries of B6C3F1 mice were exposed to lysophosphatidic acid in the presence and absence of 0.3 % fetal bovine serum for measurement of cumulus expansion and released hyaluronan, respectively. Results: Exogenously added lysophosphatidic acid concentration-dependently stimulated production of hyaluronan in the cumulus cell-oocyte complex, and the stimulatory effect of lysophosphatidic acid on hyaluronan production was mediated through the signal pathways, including LPA receptor-Gi coupling, EGF receptor transactivation, and activations of phosphatidylinositol-specific phospholipase C, protein kinase C and mitogen-activated protein kinases. LPA increased mRNA expression of tumor necrosis α-induced protein 6, a hyaluronan-binding protein, and expansion of cumulus cell-oocyte complex. Conclusions: Lysophosphatidic acid in follicular fluids may participate in physiological cumulus expansion before ovulation by stimulating production of hyaluronan and proteins that enable the association of hyaluronan with cumulus cells and oocytes.
Purpose: In mammals, cumulus expansion due to increased synthesis of hyaluronan was suggested to correlate with modification of the gap junction between cumulus cells and the oocyte, leading to cumulus expansion. We examined whether lysophosphatidic acid, a lipid mediator detected in mammalian body fluids, stimulates significant production of hyaluronan and thus affects mouse cumulus expansion in vitro. Methods: Cumulus-oocyte complexes isolated from the gonadotropin-treated ovaries of B6C3F1 mice were exposed to lysophosphatidic acid in the presence and absence of 0.3 % fetal bovine serum for measurement of cumulus expansion and released hyaluronan, respectively. Results: Exogenously added lysophosphatidic acid concentration-dependently stimulated production of hyaluronan in the cumulus cell-oocyte complex, and the stimulatory effect of lysophosphatidic acid on hyaluronan production was mediated through the signal pathways, including LPA receptor-Gi coupling, EGF receptor transactivation, and activations of phosphatidylinositol-specific phospholipase C, protein kinase C and mitogen-activated protein kinases. LPA increased mRNA expression of tumor necrosis α-induced protein 6, a hyaluronan-binding protein, and expansion of cumulus cell-oocyte complex. Conclusions: Lysophosphatidic acid in follicular fluids may participate in physiological cumulus expansion before ovulation by stimulating production of hyaluronan and proteins that enable the association of hyaluronan with cumulus cells and oocytes.