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Endocrinology, doi:10.1210/en.2005-0309
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Endocrinology Vol. 146, No. 10 4437-4444
Copyright © 2005 by The Endocrine Society

Cyclic Adenosine 3',5'-Monophosphate-Dependent Activation of Mitogen-Activated Protein Kinase in Cumulus Cells Is Essential for Germinal Vesicle Breakdown of Porcine Cumulus-Enclosed Oocytes

Cheng-Guang Liang, Li-Jun Huo, Zhi-Sheng Zhong, Da-Yuan Chen, Heide Schatten and Qing-Yuan Sun

State Key Laboratory of Reproductive Biology, Institute of Zoology (C.-G.L., L.-J.H., D.-Y.C., Q.-Y.S.), and Graduate School (C.-G.L., L.-J.H.), Chinese Academy of Sciences, Beijing 100080, China; and Department of Veterinary Pathobiology (Z.-S.Z., H.S.), University of Missouri-Columbia, Columbia, Missouri 65211

Address all correspondence and requests for reprints to: Qing-Yuan Sun, Ph.D., State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100080, China. E-mail: sunqy1{at}yahoo.com; or sunqy{at}ioz.ac.cn.

MAPK plays an important role during meiotic maturation in mammalian oocytes, whereas the necessity of MAPK during meiotic resumption in porcine oocytes is still controversial. Here, by applying the method of ultracentrifugation to move the opaque lipid droplets to the edge of the oocyte, therefore allowing clear visualization of porcine germinal vesicles, oocytes just before germinal vesicle breakdown (GVBD) and those that had just undergone GVBD were selected for the assay of MAPK activation. Our results showed that phosphorylation of MAPK in oocytes occurred after GVBD in all three different culture models: spontaneous maturation model, inhibition-induction maturation model, and normal maturation model. Moreover, we found that activation of MAPK in cumulus cells but not in oocytes was essential for GVBD in cumulus-enclosed oocytes. Then the cross-talk between cAMP and MAPK in cumulus cells was investigated by using cell-type-specific phosphodiesterase (PDE) isoenzyme inhibitors. Our results showed that PDE3 subtype existed in oocytes, whereas PDE4 subtype existed in cumulus cells. PDE3 inhibitor prevented meiotic resumption of oocytes, whereas PDE4 inhibitor enhanced the ability of FSH or forskolin to activate MAPK in cumulus cells. We propose that increased cAMP resulting from inhibition of PDE3 in oocytes blocks GVBD, whereas increased cAMP resulting from inhibition of PDE4 activates MAPK pathway in cumulus cells, which is essential for GVBD induction.




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