Journal article
WNT/β-catenin and p27/FOXL2 differentially regulate supporting cell proliferation in the developing ovary
SE Gustin, K Hogg, JM Stringer, RH Rastetter, E Pelosi, DC Miles, AH Sinclair, D Wilhelm, PS Western
Developmental Biology | Published : 2016
Abstract
Sexual development is initiated through differentiation of testicular Sertoli cells or ovarian granulosa cells. Although these supporting cells are considered to develop from common bipotential precursors, recent evidence suggests that distinct supporting cell populations are present in the ovary, with one providing granulosa cells of the medullary follicles and the other providing granulosa cells of the cortical follicles, the latter of which support lifelong fertility. Here, we demonstrate that XX fetal gonads contain GATA4 expressing supporting cells that either enter mitotic arrest, or remain proliferative. Blocking WNT signalling reduces XX supporting cell proliferation, while stabilisi..
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Grants
Awarded by National Institutes of Health
Funding Acknowledgements
This work was supported by the Monash University Faculty of Medicine, Nursing and Health Sciences and NHMRC Grant #1043939 to PW, the Victorian Government's Operational Infrastructure Support Program, an NHMRC Program grant awarded to AS and the Intramural Research Program of the National Institute on Aging, NIH. DW is supported by an ARC Future Fellowship (FT110100327). D.C.M. is supported by NHMRC Early Career Fellowship (Grant #1052195).