Early in mammalian ovarian follicular development, granulosa cells associate with both the oocyte and the basal lamina that circumscribes the follicle. Later, however, during the development of the antrum, the granulosa cells become divided into two major groups: those in contact with the oocyte (cumulus granulosa cells) and those in contact with the basal lamina (mural granulosa cells). Although abundant information on the role of granulosa cells in oocyte development has emerged in the last decade, little is known of how the oocyte or basal lamina might participate in granulosa cell development. The principal hypothesis to be tested in the proposed studies is that granulosa cell development and function are modulated by contact with the oocyte or the basal lamina. The first specific aim is to determine whether removal of the oocyte affects the development and function of granulosa cells from preantral follicles. A unique system has been developed to assess the effects of oocytectomy on cultured oocyte-granulosa cell complexes from 10 day old mice. Potential effects will assessed in terms of cell proliferation, protein synthetic patterns, and the responses of the cells to gonadotropin stimulation. The cumulus and mural granulosa and antral follicles produce some type-specific proteins and respond in some different ways to hormonal stimulation. These differences could be promoted by many diverse developmental stimuli. This proposal focuses on two factors that could participate in the differential expression of mural and cumulus granulosa cell-specific proteins; (1) development from different progenitor cells, and (2) association with either the oocyte or the basal lamina. Aggregation chimeras will be prepared from 8-cell embryos of two congenic lines expression- expressing different isozyme alleles at the glucose-6-phosphate isomerase-1 locus, and the expression of these alleles in mural and cumulus granulosa cells in female chimeras will be determined to ascertain whether these two cell types develop from on or more progenitor cells that initially contact the primordial types develop from one or more progenitor cells that initially contact the primordial oocyte during primitive follicle formation. To determine whether contact with basal lamina promotes development of mural granulosa cells, and whether the absence of such promotes development as cumulus granulosa cells, granulosa cell development will be assessed by 2-dimensional polyacrylamide gel electrophoresis of proteins synthesized by cells grown in contact with basal lamina or under conditions that prevent cell adhesion to substratum.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD023839-05
Application #
3324160
Study Section
Reproductive Biology Study Section (REB)
Project Start
1988-02-03
Project End
1994-01-31
Budget Start
1992-02-01
Budget End
1994-01-31
Support Year
5
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609
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Wigglesworth, Karen; Lee, Kyung-Bon; Emori, Chihiro et al. (2015) Transcriptomic diversification of developing cumulus and mural granulosa cells in mouse ovarian follicles. Biol Reprod 92:23
Peng, Jia; Wigglesworth, Karen; Rangarajan, Adithya et al. (2014) Amino acid 72 of mouse and human GDF9 mature domain is responsible for altered homodimer bioactivities but has subtle effects on GDF9:BMP15 heterodimer activities. Biol Reprod 91:142
Peng, Jia; Li, Qinglei; Wigglesworth, Karen et al. (2013) Reply to Mottershead et al.: GDF9:BMP15 heterodimers are potent regulators of ovarian functions. Proc Natl Acad Sci U S A 110:E2258
Emori, Chihiro; Wigglesworth, Karen; Fujii, Wataru et al. (2013) Cooperative effects of 17?-estradiol and oocyte-derived paracrine factors on the transcriptome of mouse cumulus cells. Endocrinology 154:4859-72
Lee, Kyung-Bon; Zhang, Meijia; Sugiura, Koji et al. (2013) Hormonal coordination of natriuretic peptide type C and natriuretic peptide receptor 3 expression in mouse granulosa cells. Biol Reprod 88:42
Wigglesworth, Karen; Lee, Kyung-Bon; O'Brien, Marilyn J et al. (2013) Bidirectional communication between oocytes and ovarian follicular somatic cells is required for meiotic arrest of mammalian oocytes. Proc Natl Acad Sci U S A 110:E3723-9
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Peng, Jia; Li, Qinglei; Wigglesworth, Karen et al. (2013) Growth differentiation factor 9:bone morphogenetic protein 15 heterodimers are potent regulators of ovarian functions. Proc Natl Acad Sci U S A 110:E776-85
Zhang, Meijia; Su, You-Qiang; Sugiura, Koji et al. (2011) Estradiol promotes and maintains cumulus cell expression of natriuretic peptide receptor 2 (NPR2) and meiotic arrest in mouse oocytes in vitro. Endocrinology 152:4377-85

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