Department of Endocrinology, Hospital Infantil Universitario Niño Jesús, Instituto de Investigación la Princesa, Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutriciόn (CIBEROBN), Instituto de Salud Carlos III, and IMDEA Food Institute, CEIUAM+CSIC, Madrid, Spain.
Instituto Cajal, Consejo Superior de Investigaciones Científicas (CSIC) and Centro de Investigación Biomédica en Red de Fragilidad y Envejecimiento Saludable (CIBERFES), Instituto de Salud Carlos III, Madrid, Spain.
Mech Ageing Dev. 2021 Jun;196:111473. doi: 10.1016/j.mad.2021.111473. Epub 2021 Mar 22.
Diseases and aging-associated alterations of the nervous system often show sex-specific characteristics. Glial cells play a major role in the endogenous homeostatic response of neural tissue, and sex differences in the glial transcriptome and function have been described. Therefore, the possible role of these cells in the generation of sex differences in pathological alterations of the nervous system is reviewed here. Studies have shown that glia react to pathological insults with sex-specific neuroprotective and regenerative effects. At least three factors determine this sex-specific response of glia: sex chromosome genes, gonadal hormones and neuroactive steroid hormone metabolites. The sex chromosome complement determines differences in the transcriptional responses in glia after brain injury, while gonadal hormones and their metabolites activate sex-specific neuroprotective mechanisms in these cells. Since the sex-specific neuroprotective and regenerative activity of glial cells causes sex differences in the pathological alterations of the nervous system, glia may represent a relevant target for sex-specific therapeutic interventions.
神经系统疾病和与衰老相关的改变通常表现出性别特异性特征。神经胶质细胞在神经组织的内源性稳态反应中起着重要作用,并且已经描述了胶质细胞转录组和功能的性别差异。因此,在这里回顾了这些细胞在神经病理改变中产生性别差异中的可能作用。研究表明,神经胶质细胞对病理损伤的反应具有性别特异性的神经保护和再生作用。至少有三个因素决定了胶质细胞的这种性别特异性反应:性染色体基因、性腺激素和神经活性甾体激素代谢物。性染色体组成决定了脑损伤后胶质细胞转录反应的差异,而性腺激素及其代谢物激活了这些细胞中的性别特异性神经保护机制。由于神经胶质细胞的性别特异性神经保护和再生活性导致了神经系统病理改变中的性别差异,因此神经胶质细胞可能是性别特异性治疗干预的一个相关靶点。