4.7 Article

Stress Hormone Corticosterone Controls Metabolic Mitochondrial Performance and Inflammatory Signaling of In Vitro Cultured Sertoli Cells

期刊

BIOMEDICINES
卷 10, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/biomedicines10092331

关键词

male fertility; Sertoli cell; stress; corticosterone; metabolism; mitochondria; interleukine-6

资金

  1. Fundacao para a Ciencia e a Tecnologia (FCT) [UIDB/50006/2020, UIDB/00215/2020, UIDP/00215/2020, LA/P/0064/2020, 2021.03439.CEECIND, CEECINST/00026/2018]
  2. Coordination for the Improvement of Higher Education Personnel (CAPES)
  3. EU
  4. FEDER-European Regional Development Fund, through the COMPETE Programme (Operational Programme for Competitiveness)
  5. FCT-Fundacao para a Ciencia e a Tecnologia (Portuguese Foundation for Science and Technology) [REEQ/481/QUI/2006, RECI/QEQ-QFI/0168/2012, CENTRO-07-CT62-FEDER-002012]
  6. Rede Nacional de Ressonancia Magnetica Nuclear (RNRMN)

向作者/读者索取更多资源

Stress and its associated hormones, such as cortisol and corticosterone, have a significant impact on reproductive functions. In this study, the researchers examined the effects of corticosterone on Sertoli cells in the testes. They found that low concentrations of corticosterone promoted glycolytic activity in the cells, without affecting cell redox power and mitochondrial respiration. Additionally, corticosterone influenced the expression of the pro-inflammatory cytokine IL-6. These findings suggest that corticosterone plays a role in regulating the energy balance of Sertoli cells, which may ultimately impact spermatogenic performance.
Stress, as a physiological response, is a major factor that affects several processes, including reproductive functions. The main hormonal players of stress are cortisol (humans) and corticosterone (rodents). Sertoli cells (SCs), as key contributors for the testicular homeostasis maintenance, are extensively challenged by different hormones, with glucocorticoid corticosterone being the signaling modulator that may impact these cells at different levels. We aimed to characterize how corticosterone modulates SCs energy balance, putting the mitochondrial performance and signaling output in perspective as the cells can disperse to the surroundings. TM4 mouse SCs were cultured in the absence and presence of corticosterone (in nM: 20, 200, and 2000). Cells were assessed for extracellular metabolic fluxes, mitochondrial performance (cell respirometry, mitochondrial potential, and mitochondrial complex expressions and activities), and the expression of androgen and corticosteroid receptors, as well as interleukine-6 (IL-6) and glutathione content. Corticosterone presented a biphasic impact on the extracellular fluxes of metabolites. Low sub-physiological corticosterone stimulated the glycolytic activity of SCs. Still, no alterations were perceived for lactate and alanine production. However, the lactate/alanine ratio was decreased in a dose-dependent mode, opposite to the mitochondrial complex II activity rise and concurrent with the decrease of IL-6 expression levels. Our results suggest that corticosterone finely tuned the energetic profile of mouse SCs, with sub-physiological concentrations promoting glycolytic expenditure, without translating into cell redox power and mitochondrial respiratory chain performance. Corticosterone deeply impacted the expression of the pro-inflammatory IL-6, which may alter cell-to-cell communication in the testis, in the last instance and impact of the spermatogenic performance.

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