Department of Microscopy, Laboratory of Cell Biology, and Unit for Multidisciplinary Research in Biomedicine, Institute of Biomedical Sciences Abel Salazar, University of Porto, Porto, Portugal.
Department of Genetics, Faculty of Medicine, University of Porto, Porto, Portugal.
J Cell Physiol. 2021 Jul;236(7):5265-5277. doi: 10.1002/jcp.30230. Epub 2020 Dec 23.
The strong hormonal dysregulation associated with obesity is responsible for the disruption of several reproductive events. Sertoli cells (SCs) function is dependent on energetic homeostasis and thus, directly associated with energy homeostasis regulating hormones. To further understand the influence of those hormones with SCs function and obesity, we hypothesize that human SCs express obesity-related genes (ORG; MC4R, GNPDA2, TMEM18, and FTO) and that they respond to energy homeostasis regulating hormones (leptin, ghrelin, and glucagon-like protein 1 [GLP-1]) stimuli. To test our hypothesis, SCs were cultured with increasing doses of leptin (0, 5, 25, or 50 ng/ml, for 24 h), ghrelin (0, 20, 100, and 500 pM, for 24 h), and GLP-1 (10, 1000, or 1 × 105 pM, for 6 h). The presence and abundance of ORG transcripts and proteins in SCs were accessed by polymerase chain reaction techniques, Western blot analysis, and immunofluorescence staining. Our results show that human SCs express MC4R, GNPDA2, TMEM18, and FTO in specific cellular locations. MC4R and FTO expression in human SCs was not responsive to the treatments. However, GNPDA2 and TMEM18 expression increased after exposure to the highest concentration of leptin and ghrelin, respectively. We highlight for the first time that human SCs express ORG and that these are responsive to energy homeostasis hormonal stimuli. GNPDA2 and TMEM18 expression respond in opposite directions according to overall energy status, mediated by energy homeostasis regulating hormones. Leptin and ghrelin control of ORG expression by human SCs can be associated with overweight-related infertility and subfertility in males.
肥胖相关的强烈激素失调会破坏多个生殖事件。支持细胞(SCs)的功能依赖于能量平衡,因此与调节能量平衡的激素直接相关。为了进一步了解这些激素对SCs 功能和肥胖的影响,我们假设人类SCs 表达肥胖相关基因(ORG;MC4R、GNPDA2、TMEM18 和 FTO),并且它们对调节能量平衡的激素(瘦素、胃饥饿素和胰高血糖素样肽 1 [GLP-1])刺激有反应。为了验证我们的假设,我们用不同剂量的瘦素(0、5、25 或 50ng/ml,24 小时)、胃饥饿素(0、20、100 和 500pM,24 小时)和 GLP-1(10、1000 或 1×105pM,6 小时)培养SCs。通过聚合酶链反应技术、Western blot 分析和免疫荧光染色来检测 ORG 转录本和蛋白质在SCs 中的存在和丰度。我们的结果表明,人类SCs 在特定的细胞位置表达 MC4R、GNPDA2、TMEM18 和 FTO。人类SCs 中的 MC4R 和 FTO 表达对这些处理没有反应。然而,GNPDA2 和 TMEM18 的表达在分别暴露于最高浓度的瘦素和胃饥饿素后增加。我们首次强调人类SCs 表达 ORG,并且这些基因对能量平衡激素刺激有反应。根据整体能量状态,GNPDA2 和 TMEM18 的表达以相反的方向对能量平衡调节激素做出反应。瘦素和胃饥饿素对人类SCs ORG 表达的控制可能与男性超重相关的不孕和不育有关。