Faculty, Staff and Student Publications

Publication Date

5-9-2024

Journal

Biology of Reproduction

Abstract

It has been previously shown that the cytokine interleukin 33 is required for two processes, i.e., autophagic digestion of granulosa cells and recruitment of macrophages into atretic follicles, for full disposal of atretic follicles. Now, this study shows that activation of interleukin 33-suppression of tumorigenicity 2-Nuclear Factor ĸB (NFκB) axis in granulosa in early atretic follicles may regulate those two events. Injection of human chorionic gonadotropin has been shown to induce a transient peak of interleukin 33 expression with synchronized atresia. In this model, interleukin 33-independent expression of suppression of tumorigenicity 2 in granulosa cells was detected in early atretic follicles before macrophage invasion. The activation of NFκB pathway in ovaries was further demonstrated in vivo in Tg mice with luciferase-reporter for NFκB activation; the activation was microscopically localized to granulosa cells in early atretic follicles. Importantly, antibody blockage of interleukin 33 or interleukin 33 Knock-out (KO) (Il33-/-) not only inhibited NFκB activity in ovaries, but it also altered expression of two key genes, i.e., reduction in proinflammatory interleukin6 (IL6) expression, and a surge of potential autophagy-inhibitory mammalian target of rapamycin (mTOR) expression in atretic follicles. By contrast, apoptosis and other genes, such as interleukin1β (IL1β) were not affected. In conclusion, in parallel to apoptosis, atresia signals also trigger activation of the interleukin 33-suppression of tumorigenicity 2-NFκB pathway in granulosa, which leads to (1) down-regulated expression of mTOR that is a negative regulator of autophagy and (2) up-regulated expression of proinflammatory IL6.

Keywords

Female, Animals, Granulosa Cells, Mice, NF-kappa B, Follicular Atresia, Ovarian Follicle, Interleukin-33, Signal Transduction, Mice, Knockout, Autophagy, IL33, ST2, NFκB, granulosa, atresia, tissue disposal

DOI

10.1093/biolre/ioae015

PMID

38271626

PMCID

PMC11094390

PubMedCentral® Posted Date

1-25-2024

PubMedCentral® Full Text Version

Post-print

ioae015ga1.jpg (66 kB)
Graphical Abstract

Published Open-Access

yes

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