4.4 Article

Hormone regulation of thrombospondin-1 mRNA in porcine granulosa cells in vitro

Journal

ANIMAL REPRODUCTION SCIENCE
Volume 244, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.anireprosci.2022.107048

Keywords

Thrombospondin-1 (THBS1); Granulosa cell; Follicular growth; Porcine

Funding

  1. NICHD, National Institutes of Health [R15-HD-066302]
  2. Oklahoma State University Agricultural Exp. Station

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This study investigated the effects of different hormones on THBS1 gene expression in porcine granulosa cells and the changes of THBS1 mRNA during follicular development. The results showed that FSH, IGF1, and FGF9 inhibited THBS1 mRNA expression, while PGE2 promoted THBS1 mRNA expression. The study also found that the abundance of THBS1 mRNA was higher in large follicles compared to small and medium-sized follicles.
Thrombospondin-1 (THBS1) is involved in the process of angiogenesis and is down-regulated by insulin-like growth factor 1 (IGF1) in porcine granulosa cells (GC), but what other hormones regulate GC THBS1 and its role in follicular growth is unclear. Thus, six experiments were conducted to determine the influence of other hormones on THBS1 gene expression in porcine GC, and to determine if THBS1 mRNA changes during follicular development. For Exp. 1-5, small (1-5 mm) follicles from ovaries of abattoir gilts were aspirated, GC collected and treated with FSH, IGF1, fibroblast growth factor 9 (FGF9), Sonic hedgehog (SHH), estradiol, cortisol, and/or prostaglandin E2 (PGE2). FSH, IGF1 and FGF9 each decreased (P < 0.05) THBS1 mRNA abundance. Alone, PGE2 increased (P < 0.05) THBS1 mRNA abundance. PGE2 significantly attenuated the FSH-induced inhibition of THBS1 mRNA expression. Estradiol, cortisol, and SHH had no effect on THBS1 mRNA abundance. In Exp. 6, small (1-3 mm), medium (4-6 mm) and large (7-14 mm) follicles were aspirated to measure abundance of THBS1 mRNA in GC which did not differ (P > 0.10) between small and medium-sized follicles but was threefold greater (P < 0.05) in large compared to small or medium follicles. We hypothesize that the inhibitory effects of FSH, IGF1 and FGF9 on the antiangiogenic gene THBS1 could contribute to promoting angiogenesis in the developing follicle, while stimulation of THBS1 mRNA by PGE2 may help reduce angiogenesis during the preovulatory period when PGE2 and THBS1 mRNA are at their greatest levels.

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