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Phosphorylation and inactivation of glycogen synthase kinase-3 by soluble kit ligand in mouse oocytes during early follicular development.

Liu, Lian (author)
Rajareddy, Singareddy (author)
Umeå universitet,Institutionen för medicinsk kemi och biofysik
Reddy, Pradeep (author)
Umeå universitet,Institutionen för medicinsk kemi och biofysik
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Jagarlamudi, Krishna (author)
Umeå universitet,Institutionen för medicinsk kemi och biofysik
Du, Chun (author)
Shen, Yan (author)
Guo, Yongzhi (author)
Umeå universitet,Institutionen för medicinsk kemi och biofysik
Boman, Karin (author)
Umeå universitet,Institutionen för strålningsvetenskaper,Onkologi
Lundin, Eva (author)
Patologi
Ottander, Ulrika (author)
Umeå universitet,Obstetrik och gynekologi
Selstam, Gunnar (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten),Selstam
Liu, Kui (author)
Umeå universitet,Institutionen för medicinsk kemi och biofysik
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 (creator_code:org_t)
Bioscientifica, 2007
2007
English.
In: Journal of Molecular Endocrinology. - : Bioscientifica. - 0952-5041 .- 1479-6813. ; 38:1-2, s. 137-146
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Communication between mammalian oocytes and their surrounding granulosa cells through the Kit-Kit ligand (KL, or stem cell factor, SCF) system has been shown to be crucial for follicular development. Our previous studies (Reddy et al. 2005, Liu et al. 2006) have indicated that the intra-oocyte KL-Kit-PI3 kinase (PI3K)-Akt-Foxo3a cascade may play an important role in follicular activation and early development. In the present study, using in situ hybridization and in vitro culture of growing oocytes from 8-day-old postnatal mice, we have demonstrated that another Akt substrate, glycogen synthase kinase-3 (GSK-3), is expressed in growing oocytes. Also, treatment of cultured mouse oocytes with soluble KL not only leads to increased Akt kinase activity in the oocytes, which can phosphorylate recombinant GSK-3 in vitro, but also leads to phosphorylation of oocyte GSK-3alpha and GSK-3beta, which can result in the inactivation of GSK-3 function in oocytes. In addition, we have shown that the regulation of GSK-3alpha and GSK-3beta in cultured oocytes by soluble KL is accomplished through PI3K, since the PI3K-specific inhibitor LY294002 completely abolished the KL-induced phosphorylation of GSK-3alpha and GSK-3beta. Moreover, blockage of the Kit signaling pathway by a Kit function-blocking antibody, ACK2, resulted in reduced phosphorylation of GSK-3. Taken together, our data suggest that the cascade from granulosa cell-derived KL to Kit-PI3K-Akt-GSK-3 in oocytes may take part in regulation of oocyte growth and early ovarian follicular development.

Keyword

Animals
Female
Glycogen Synthase Kinase 3/*antagonists & inhibitors/metabolism
Mice
Mice; Inbred C57BL
Oocytes/*enzymology
Ovarian Follicle/*enzymology
Phosphorylation
Proto-Oncogene Proteins c-akt/physiology
Stem Cell Factor/*physiology

Publication and Content Type

ref (subject category)
art (subject category)

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