Activation of interleukin 33-NFκB axis in granulosa cells during atresia and its role in disposal of atretic follicles

• Published in: Biology of reproduction 2024-05, Vol.110 (5), p.924-935
• Main Authors: Wu, Jean, Carlock, Colin, Tatum, Kiana, Shim, Junbo, Zhou, Cindy, Lou, Yahuan
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; atresia; Autophagy; Autophagy - physiology; Cell activation; Chorionic gonadotropin; Cytokines; Female; Follicles; Follicular Atresia - metabolism; Gonadotropins; granulosa; Granulosa cells; Granulosa Cells - drug effects; Granulosa Cells - metabolism; IL33; Inflammation; Interleukin-33 - genetics; Interleukin-33 - metabolism; Macrophages; Mice; Mice, Knockout; NF-kappa B - metabolism; NF-κB protein; NFκB; Ovarian Follicle - metabolism; Ovaries; Pituitary (anterior); Rapamycin; RESEARCH ARTICLE; Signal Transduction; ST2; tissue disposal; TOR protein; Tumorigenicity
• ISSN: 0006-3363; 1529-7268; 1529-7268
• DOI: 10.1093/biolre/ioae015

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 KB (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. Summary Sentence Interleukin 33–suppression of tumorigenicity 2–NFκB axis is activated in granulosa cells of early atretic follicles to downregulate mTOR, which, in turn, intensifies autophagic digestion of atretic follicles for self-disposal. Graphical Abstract