Reboldi Andrea, Dang Eric
Department of Pathology, University of Massachussetts Medical School, Worcester, Massachusetts, 01605, USA.
Department of Biochemistry and Biophysics, University of California, San Francisco, California, 94158, USA.
F1000Res. 2018 Oct 16;7. doi: 10.12688/f1000research.15500.1. eCollection 2018.
It has been long recognized that cholesterol is a critical molecule in mammalian cell biology, primarily for its contribution to the plasma membrane's composition and its role in assuring proper transmembrane receptor signaling as part of lipid rafts. Efforts have also been made to characterize the cholesterol biosynthetic pathway, cholesterol homeostasis, and cholesterol-derived metabolites in order to gain insights into their dysregulation during metabolic diseases. Despite the central role cholesterol metabolism plays in shaping human health, its regulation during immune activation, such as immune response to pathogens or autoimmune/autoinflammatory diseases, is poorly understood. The immune system is composed of several type of cells with distinct developmental origin, life span, molecular requirements, and gene expressions. It is unclear whether the same array of cholesterol metabolism regulators are equally employed by different immune cells and whether distinct cholesterol metabolites have similar biological consequences in different immune cells. In this review, we will describe how cholesterol metabolism is controlled during the adaptive and the innate immune response and the role for intracellular and extracellular receptors for cholesterol and its derivatives.
长期以来,人们一直认识到胆固醇是哺乳动物细胞生物学中的关键分子,主要是因为它对质膜组成的贡献以及作为脂筏一部分在确保跨膜受体信号传导正常方面所起的作用。人们还致力于表征胆固醇生物合成途径、胆固醇稳态和胆固醇衍生代谢物,以便深入了解它们在代谢疾病期间的失调情况。尽管胆固醇代谢在塑造人类健康方面起着核心作用,但其在免疫激活过程中的调节,如对病原体的免疫反应或自身免疫/自身炎症性疾病,仍知之甚少。免疫系统由几种具有不同发育起源、寿命、分子需求和基因表达的细胞类型组成。目前尚不清楚不同的免疫细胞是否同样利用了相同的胆固醇代谢调节因子阵列,以及不同的胆固醇代谢物在不同的免疫细胞中是否具有相似的生物学后果。在这篇综述中,我们将描述在适应性免疫和先天性免疫反应过程中胆固醇代谢是如何被控制的,以及胆固醇及其衍生物的细胞内和细胞外受体所起的作用。