RESEARCH 2006
RESEARCH 2005
RESEARCH 2004
RESEARCH 2003
> Dr. James Anderson
> Dr. James Buchanan
> Dr. James Courtright
> Dr. Jane E. Dorweiler
> Dr. Stephen Downs
> Dr. Robert Fitts
> Dr. James Maki
   - Alissa R. DeHaan
   - Jenny Strickland
> Dr. Michael Schläppi 
> Dr. Rosemary A. Stuart
> Dr. Gail Waring
> Dr. Pinfen Yang
   - Zagum Bhatti
   - Jennifer Dienes
   - Susan R. Hupp

RESEARCH 2002
RESEARCH 2001
RESEARCH 2000

 

 

Involvement of MAPK in the Induction of Meiotic Maturation of Incompetent Oocytes

Lindsey Heim
Luther College
Decorah, IA
Mentor: Dr. Stephen Downs

At birth, mouse oocytes are arrested in prophase I of meiosis. In fully grown oocytes, the release of the oocyte from its surrounding follicular environment results in the spontaneous resumption of meiosis, or meiotic maturation. In contrast to these fully grown, competent oocytes, growing oocytes from more immature stages of follicular development will not spontaneously resume meiosis, and are designated as incompetent. 

Although incompetent oocytes do not resume meiosis spontaneously, they can be stimulated to undergo maturation with various compounds. AICA riboside has been shown in previous studies in this laboratory to stimulate meiotic maturation in dbcAMP arrested compotent oocytes by the activation of AMPK, and it is shown here that AICA riboside will also induce meiotic maturation in incompetent oocytes. Additionally, it has been demonstrated that meiotic maturation can be stimulated by activation of AMPK with rosiglitazone, an anti-diabetic agent. Okadaic acid, a phosphatase inhibitor, stimulates maturation in incompotent oocytes by the activation of mitogen-activated protein kinase (MAPK). It is also shown here that by using the specific inhibitors of MAPK, U0126 and PD98059, okadaic acid and AICA riboside induced maturation can be partially inhibited. These results suggest a potential role of MAPK activation in the meiotic maturation of incompetent oocytes. 


 

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