Crisóstomo Luís, Alves Marco G, Gorga Agostina, Sousa Mário, Riera María F, Galardo María N, Meroni Silvina B, Oliveira Pedro F
Unit for Multidisciplinary Research in Biomedicine (UMIB), Laboratory of Cell Biology, Department of Microscopy, Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, Porto, Portugal.
Department of Genetics, Faculty of Medicine (FMUP), University of Porto, Porto, Portugal.
Methods Mol Biol. 2018;1748:129-155. doi: 10.1007/978-1-4939-7698-0_11.
Sertoli cells play a central role in spermatogenesis. They maintain the blood-testis barrier, an essential feature of seminiferous tubules which creates the proper environment for the occurrence of the spermatogenesis. However, this confinement renders germ cells almost exclusively dependent on Sertoli cells' nursing function and support. Throughout spermatogenesis, differentiating sperm cells become more specialized, and their biochemical machinery is insufficient to meet their metabolic demands. Although the needs are not the same at all differentiation stages, Sertoli cells are able to satisfy their needs. In order to maintain the seminiferous tubule energetic homeostasis, Sertoli cells react in response to several metabolic stimuli, through signaling cascades. The AMP-activated kinase, sensitive to the global energetic status; the hypoxia-inducible factors, sensitive to oxygen concentration; and the peroxisome proliferator-activated receptors, sensitive to fatty acid availability, are pathways already described in Sertoli cells. These cells' metabolism also reflects the whole-body metabolic dynamics. Metabolic diseases, including obesity and type II diabetes mellitus, induce changes that, both directly and indirectly, affect Sertoli cell function and, ultimately, (dys)function in male reproductive health. Insulin resistance, increased estrogen synthesis, vascular disease, and pubic fat accumulation are examples of metabolic-related conditions that affect male fertility potential. On the other hand, malnutrition can also induce negative effects on male sexual function. In this chapter, we review the molecular mechanisms associated with the nutritional state and male sexual (dys)function and the central role played by the Sertoli cells.
支持细胞在精子发生过程中起着核心作用。它们维持血睾屏障,这是生精小管的一个基本特征,为生精过程创造了适宜的环境。然而,这种隔离使得生殖细胞几乎完全依赖支持细胞的滋养功能和支持。在整个精子发生过程中,分化中的精子细胞变得更加特化,其生化机制不足以满足其代谢需求。尽管在所有分化阶段需求不尽相同,但支持细胞能够满足它们的需求。为了维持生精小管的能量稳态,支持细胞通过信号级联反应对几种代谢刺激做出反应。对整体能量状态敏感的AMP激活激酶、对氧浓度敏感的缺氧诱导因子以及对脂肪酸可用性敏感的过氧化物酶体增殖物激活受体,都是已在支持细胞中描述的信号通路。这些细胞的代谢也反映了全身的代谢动态。包括肥胖和II型糖尿病在内的代谢性疾病会引发直接或间接影响支持细胞功能的变化,并最终影响男性生殖健康的(功能)失调。胰岛素抵抗、雌激素合成增加、血管疾病和耻骨脂肪堆积都是影响男性生育潜力的代谢相关病症的例子。另一方面,营养不良也会对男性性功能产生负面影响。在本章中,我们综述了与营养状态和男性性(功能)失调相关的分子机制以及支持细胞所起的核心作用。