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1 June 2004 Cell-Specific Expression and Regulation of Soluble Guanylyl Cyclase α1 and β1 Subunits in the Rat Ovary
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Abstract

Soluble guanylyl cyclase (sGC) is activated by nitric oxide (NO) and carbon monoxide, resulting in cGMP production. Recent studies indicate that NO and cGMP influence ovarian functions. However, little information is available regarding the ovarian expression of sGC. The present study examined sGC α1 and β1 subunit protein levels in the ovary during postnatal development, gonadotropin-induced follicle growth, ovulation, and luteinization as well as in cultured rat granulosa cells. In postnatal rats, sGC α1 subunit immunoreactivity was high in granulosa cells of primordial and primary follicles on Day 5 but low in granulosa cells of larger follicles on Days 10 and 19. Theca cells of developing follicles, but not stromal cells, also demonstrated moderate sGC α1 immunoreactivity. In gonadotropin- treated immature rats, intense sGC α1 subunit staining was similarly observed in granulosa cells of primordial and primary follicles, but such staining was low in granulosa cells of small antral follicles and undetectable in granulosa cells of large antral and preovulatory follicles. Following ovulation, corpora lutea expressed moderate sGC α1 immunoreactivity. Similar ovarian localization and expression patterns were seen for sGC β1, indicating regulated coexpression of sGC subunits. Immunoblot analysis revealed no change in total ovarian sGC α1 and β1 subunit protein levels during gonadotropin treatment. Similarly, no effect of FSH on sGC subunit protein levels was apparent in cultured granulosa cells. These findings indicate regulated, cell- specific patterns of sGC expression in the ovary and are consistent with roles for cGMP in modulating ovarian functions.

Fangxiong Shi, Robert L. Stewart, Emerson Perez, Jean Y-H. Chen, and Philip S. LaPolt "Cell-Specific Expression and Regulation of Soluble Guanylyl Cyclase α1 and β1 Subunits in the Rat Ovary," Biology of Reproduction 70(6), 1552-1561, (1 June 2004). https://doi.org/10.1095/biolreprod.103.025510
Received: 13 November 2003; Accepted: 1 January 2004; Published: 1 June 2004
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