Adrenomedullin: A possible regulator of germinal vesicle breakdown

Biochemical and Biophysical Research Communications

Volumn 415, Issue 4, 2011, Pages 691-695

  Hiradate, Yuuki ^a   Ohtake, Jun ^a   Hoshino, Yumi ^a   Tanemura, Kentaro ^a   Sato, Eimei ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Adrenomedullin; Akt; Cumulus cell; GVBD; Nitric oxide

Indexed keywords

ADRENOMEDULLIN; ADRENOMEDULLIN RECEPTOR; NITROPRUSSIDE SODIUM; PROTEIN KINASE B; RECEPTOR ACTIVITY MODIFYING PROTEIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; CUMULUS CELL; ENZYME INHIBITION; ENZYME PHOSPHORYLATION; FEMALE; GERMINAL VESICLE; GERMINAL VESICLE BREAKDOWN; GRANULOSA CELL; HORMONE ACTION; IMMUNOHISTOCHEMISTRY; MOUSE; NONHUMAN; OOCYTE; OOCYTE MATURATION; OVARY FOLLICLE DEVELOPMENT; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; REGULATORY MECHANISM; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SIGNAL TRANSDUCTION;

ADRENOMEDULLIN; ANIMALS; CELLS, CULTURED; CUMULUS CELLS; FEMALE; MICE; MICE, INBRED ICR; NITRIC OXIDE DONORS; NITROPRUSSIDE; OOCYTES; PROTO-ONCOGENE PROTEINS C-AKT; RECEPTORS, ADRENOMEDULLIN; RNA, MESSENGER;

EID: 84855864865     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2011.10.139     Document Type: Article

References (32)

1. Webb R.J., Marshall F., Swann K., Carroll J. Follicle-stimulating hormone induces a gap junction-dependent dynamic change in [cAMP] and protein kinase a in mammalian oocytes. Dev. Biol. 2002, 246:441-454.
2. Eppig J.J., Schultz R.M., O'Brien M., Chesnel F. Relationship between the developmental programs controlling nuclear and cytoplasmic maturation of mouse oocytes. Dev. Biol. 1994, 164:1-9.
3. Pincus G., Enzmann E.V. The comparative behavior of mammalian eggs in vivo and in vitro: I. The activation of ovarian eggs. J. Exp. Med. 1935, 62:665-675.
4. Kitamura K., Kangawa K., Kawamoto M., Ichiki K., Nakamura S., Matsuo H., Eto T. Adrenomedullin: a novel hypotensive peptide isolated from human pheochromocytoma. Biochem. Biophys. Res. Commun. 1993, 192:553-560.
5. McLatchie L.M., Fraser N.J., Main M.J., Wise A., Brown J., Thompson N., Solari R., Lee M.G., Foord S.M. RAMPs regulate the transport and ligand specificity of the calcitonin-receptor-like receptor. Nature 1998, 393:333-339.
6. Oehler M.K., Hague S., Rees M.C., Bicknell R. Adrenomedullin promotes formation of xenografted endometrial tumors by stimulation of autocrine growth and angiogenesis. Oncogene 2002, 21:2815-2821.
7. Miller M.J., Martinez A., Unsworth E.J., Thiele C.J., Moody T.W., Elsasser T., Cuttitta F. Adrenomedullin expression in human tumor cell lines. J. Biol. Chem. 1996, 271:22345-23351.
8. Li Y.Y., Li L., Hwang I.S., Tang F. Coexpression of adrenomedullin and its receptors in the reproductive system of the rat: effects on steroid secretion in rat ovary. Biol. Reprod. 2008, 79:200-208.
9. Liu J., Butzow R., Hyden-Granskog C., Voutilainen R. Expression of adrenomedullin in human ovaries, ovarian sex cord-stromal tumors and cultured granulosa-luteal cells. Gynecol. Endocrinol. 2009, 25:96-103.
10. Dotsch J., Schoof E., Schocklmann H.O., Brune B., Knerr I., Repp R., Rascher W. Nitric oxide increases adrenomedullin receptor function in rat mesangial cells. Kidney. Int. 2002, 61:1707-1713.
11. Ali N., Yousufzai S.Y., Abdel-Latif A.A. Activation of particulate guanylate cyclase by adrenomedullin in cultured SV-40 transformed cat iris sphincter smooth muscle (SV-CISM-2) cells. Cell Signal. 2000, 12:491-498.
12. Tornell J., Billig H., Hillensjo T. Resumption of rat oocyte meiosis is paralleled by a decrease in guanosine 3', 5'-cyclic monophosphate (cGMP) and is inhibited by microinjection of cGMP. Acta Physiol. Scand. 1990, 139:511-517.
13. Norris R.P., Ratzan W.J., Freudzon M., Mehlmann L.M., Krall J., Movsesian M.A., Wang H., Ke H., Nikolaev V.O., Jaffe L.A. Cyclic GMP from the surrounding somatic cells regulates cyclic AMP and meiosis in the mouse oocyte. Development 2009, 136:1869-1878.
14. Horner K., Livera G., Hinckley M., Trinh K., Storm D., Conti M. Rodent oocytes express an active adenylyl cyclase required for meiotic arrest. Dev. Biol. 2003, 258:385-396.
15. Downs S.M., Coleman D.L., Ward-Bailey P.F., Eppig J.J. Hypoxanthine is the principal inhibitor of murine oocyte maturation in a low molecular weight fraction of porcine follicular fluid. Proc. Natl. Acad. Sci. USA 1985, 82:454-458.
16. Nakamura Y., Yamagata Y., Sugino N., Takayama H., Kato H. Nitric oxide inhibits oocyte meiotic maturation. Biol. Reprod. 2002, 67:1588-1592.
17. Vaccari S., Weeks J.L., Hsieh M., Menniti F.S., Conti M. Cyclic GMP signaling is involved in the luteinizing hormone-dependent meiotic maturation of mouse oocytes. Biol. Reprod. 2009, 81:595-604.
18. Norris R.P., Freudzon M., Mehlmann L.M., Cowan A.E., Simon A.M., Paul D.L., Lampe P.D., Jaffe L.A. Luteinizing hormone causes MAP kinase-dependent phosphorylation and closure of connexin 43 gap junctions in mouse ovarian follicles: one of two paths to meiotic resumption. Development 2008, 135:3229-3238.
19. Yamagata Y., Nakamura Y., Sugino N., Harada A., Takayama H., Kishida S., Kato H. Alterations in nitrate/nitrite and nitric oxide synthase in preovulatory follicles in gonadotropin-primed immature rat. Endocrinol. J. 2002, 49:219-226.
20. Arnold W.P., Mittal C.K., Katsuki S., Murad F. Nitric oxide activates guanylate cyclase and increases guanosine 3':5'-cyclic monophosphate levels in various tissue preparations. Proc. Natl. Acad. Sci. USA 1977, 74:3203-3207.
21. Hayakawa H., Hirata Y., Kakoki M., Suzuki Y., Nishimatsu H., Nagata D., Suzuki E., Kikuchi K., Nagano T., Kangawa K., Matsuo H., Sugimoto T., Omata M. Role of nitric oxide-cGMP pathway in adrenomedullin-induced vasodilation in the rat. Hypertension 1999, 33:689-693.
22. Wangensteen R., Quesada A., Sainz J., Duarte J., Vargas F., Osuna A. Role of endothelium-derived relaxing factors in adrenomedullin-induced vasodilation in the rat kidney. Eur. J. Pharmacol. 2002, 444:97-102.
23. Berenguer C., Boudouresque F., Dussert C., Daniel L., Muracciole X., Grino M., Rossi D., Mabrouk K., Figarella-Branger D., Martin P.M., Ouafik L. Adrenomedullin, an autocrine/paracrine factor induced by androgen withdrawal, stimulates 'neuroendocrine phenotype' in LNCaP prostate tumor cells. Oncogene 2008, 27:506-518.
24. Bu S., Xia G., Tao Y., Lei L., Zhou B. Dual effects of nitric oxide on meiotic maturation of mouse cumulus cell-enclosed oocytes in vitro. Mol. Cell Endocrinol. 2003, 207:21-30.
25. Kim W., Moon S.O., Sung M.J., Kim S.H., Lee S., So J.N., Park S.K. Angiogenic role of adrenomedullin through activation of Akt, mitogen-activated protein kinase, and focal adhesion kinase in endothelial cells. FASEB J. 2003, 17:1937-1939.
26. Saskova A., Solc P., Baran V., Kubelka M., Schultz R.M., Motlik J. Aurora kinase A controls meiosis I progression in mouse oocytes. Cell Cycle 2008, 7:2368-2376.
27. Kalous J., Kubelka M., Solc P., Susor A., Motlik J. AKT (protein kinase B) is implicated in meiotic maturation of porcine oocytes. Reproduction 2009, 138:645-654.
28. Nishimatsu H., Suzuki E., Nagata D., Moriyama N., Satonaka H., Walsh K., Sata M., Kangawa K., Matsuo H., Goto A., Kitamura T., Hirata Y. Adrenomedullin induces endothelium-dependent vasorelaxation via the phosphatidylinositol 3-kinase/Akt-dependent pathway in rat aorta. Circ. Res. 2001, 89:63-70.
29. Fan H.Y., Huo L.J., Chen D.Y., Schatten H., Sun Q.Y. Protein kinase C and mitogen-activated protein kinase cascade in mouse cumulus cells: cross talk and effect on meiotic resumption of oocyte. Biol. Reprod. 2004, 70:1178-1187.
30. Del Re D.P., Miyamoto S., Brown J.H. Focal adhesion kinase as a RhoA-activable signaling scaffold mediating Akt activation and cardiomyocyte protection. J. Biol. Chem. 2008, 283:35622-35629.
31. Hakuno D., Takahashi T., Lammerding J., Lee R.T. Focal adhesion kinase signaling regulates cardiogenesis of embryonic stem cells. J. Biol. Chem. 2005, 280:39534-39544.
32. Li L., Tang F. Adrenomedullin in rat follicles and corpora lutea: expression, functions and interaction with endothelin-1. Reprod. Biol. Endcrinol. 2011, 9:111.