Regulation of serine protease inhibitor-E2 and plasminogen activator expression and secretion by follicle stimulating hormone and growth factors in non-luteinizing bovine granulosa cells in vitro

• Published in: Matrix biology Vol. 25; no. 6; pp. 342 - 354
• Main Authors: Cao, Mingju, Nicola, Edmir, Portela, Valério M., Price, Christopher A.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.08.2006
• Subjects: Animals; Bone Morphogenetic Protein 7; Bone Morphogenetic Proteins - metabolism; Cattle; Cell Line; Estradiol - metabolism; Female; Follicle; Follicle Stimulating Hormone - metabolism; Gene Expression Regulation; Granulosa; Granulosa Cells - metabolism; Growth factor; In Vitro Techniques; Insulin-Like Growth Factor I - metabolism; Intercellular Signaling Peptides and Proteins - metabolism; Ovary - metabolism; Plasminogen activator; Plasminogen Activators - chemistry; Serine Proteinase Inhibitors - pharmacology; Serpin; Serpins - chemistry; Serpins - metabolism; Transforming Growth Factor beta - metabolism; Follicle; Plasminogen activator; Serpin; Granulosa; Growth factor
• ISSN: 0945-053X; 1569-1802
• DOI: 10.1016/j.matbio.2006.05.005

During ovarian follicle growth, there is expansion of the basal lamina and changes in the follicular extracellular matrix (ECM) that are mediated in part by proteolytic enzyme cascades regulated by tissue-type plasminogen activator (tPA) and urokinase plasminogen activator (uPA). One PA inhibitor, serine protease inhibitor-E2 (SERPINE2) is expressed in granulosa but not theca cells, and expression changes with follicle development. In this study, we hypothesized that PA and SERPINE2 expression/secretion by granulosa cells are regulated by FSH and growth factors. SERPINE2 mRNA and protein levels, tPA gene expression and uPA secretion were stimulated by FSH. Insulin-like growth factor-I stimulated SERPINE2 secretion and uPA activity, and decreased secreted tPA activity and gene expression. Bone morphogenetic protein-7 increased SERPINE2 secretion and expression and tPA secretion. In contrast, fibroblast growth factor-2 inhibited tPA secretion and SERPINE2 secretion and expression. Epidermal growth factor inhibited SERPINE2 secretion and expression, but increased secreted tPA activity. Estradiol and SERPINE2 secretion were highly positively correlated, but estradiol did not alter SERPINE2 expression. These data demonstrate that SERPINE2 expression and protein secretion are regulated by FSH and growth factors in non-luteinizing bovine granulosa cells. As estradiol is a known marker of follicle health, and SERPINE2 is an anti-apoptotic factor, we propose that SERPINE2 is involved in the regulation of atresia in bovine follicles.