Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez (INCICh), Mexico City, Mexico; Postgraduate Program in Biological Sciences, Postgraduate Unit, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.
Department of Nutrition Physiology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Rev Invest Clin. 2024 Feb 15;76(2):65-79. doi: 10.24875/RIC.23000231.
Excess body weight has become a global epidemic and a significant risk factor for developing chronic diseases, which are the leading causes of worldwide morbidities. Adipose tissue (AT), primarily composed of adipocytes, stores substantial amounts of energy and plays a crucial role in maintaining whole-body glucose and lipid metabolism. This helps prevent excessive body fat accumulation and lipotoxicity in peripheral tissues. In addition, AT contains endothelial cells and a substantial population of immune cells (constituting 60-70% of non-adipocyte cells), including macrophages, T and B lymphocytes, and natural killer cells. These resident immune cells engage in crosstalk with adipocytes, contributing to the maintenance of metabolic and immune homeostasis in AT. An exacerbated inflammatory response or inadequate immune resolution can lead to chronic systemic low-grade inflammation, triggering the development of metabolic alterations and the onset of chronic diseases. This review aims to elucidate the regulatory mechanisms through which immune cells influence AT function and energy homeostasis. We also focus on the interactions and functional dynamics of immune cell populations, highlighting their role in maintaining the delicate balance between metabolic health and obesity-related inflammation. Finally, understanding immunometabolism is crucial for unraveling the pathogenesis of metabolic diseases and developing targeted immunotherapeutic strategies. These strategies may offer innovative avenues in the rapidly evolving field of immunometabolism. (Rev Invest Clin. 2024;76(2):65-79).
超重已成为全球性流行疾病,也是导致慢性疾病的重要危险因素,而慢性疾病是导致全球发病率的主要原因。脂肪组织(adipose tissue,AT)主要由脂肪细胞组成,储存大量能量,在维持全身葡萄糖和脂质代谢方面起着至关重要的作用。这有助于防止外周组织中脂肪过度积累和脂毒性。此外,脂肪组织还包含内皮细胞和大量免疫细胞(占非脂肪细胞的 60-70%),包括巨噬细胞、T 和 B 淋巴细胞以及自然杀伤细胞。这些驻留免疫细胞与脂肪细胞相互作用,有助于维持脂肪组织的代谢和免疫稳态。炎症反应过度或免疫反应不足会导致慢性全身性低度炎症,从而引发代谢改变和慢性疾病的发生。本综述旨在阐明免疫细胞影响脂肪组织功能和能量稳态的调节机制。我们还重点关注免疫细胞群体的相互作用和功能动态,强调它们在维持代谢健康与肥胖相关炎症之间微妙平衡中的作用。最后,了解免疫代谢对于揭示代谢性疾病的发病机制和开发靶向免疫治疗策略至关重要。这些策略可能为免疫代谢这一快速发展的领域提供创新途径。(Rev Invest Clin. 2024;76(2):65-79)。