Hypothalamic neuronal-glial crosstalk in metabolic disease

Linda T. Nguyen, Garron T. Dodd
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Abstract

Metabolic diseases such as obesity and type 2 diabetes affect >2 billion people worldwide, yet there are currently no effective treatments to promote remission of disease. It is therefore critical to understand the physiological and pathophysiological mechanisms underlying metabolic disease, to drive the development of effective therapeutics. Whilst the majority of research over the past few decades has focused on neurons in the hypothalamus, there is growing evidence that non-neuronal glial cells in this region play a substantial role in regulating metabolism. Here, we provide an overview of the current dogmatic view of the neuroendocrine axis governing metabolism and update this neuron-centric view to include emerging evidence implicating glial cells including tanycytes, astrocytes, microglia, and oligodendrocyte lineage cells. We discuss the latest research implicating glia in hormone transport and hypothalamic inflammation, highlighting these cells as key contributors to metabolic control and dysfunction. Glial cells therefore offer new cellular and molecular targets for future therapeutic design, to tackle metabolic disease treatment from a new perspective.

Abstract Image

代谢性疾病中的下丘脑神经元-神经胶质串扰
肥胖症和 2 型糖尿病等代谢性疾病影响着全球 20 亿人,但目前还没有有效的治疗方法来促进疾病的缓解。因此,了解代谢性疾病的生理和病理生理学机制以推动有效疗法的开发至关重要。过去几十年来,大多数研究都集中在下丘脑的神经元上,但越来越多的证据表明,该区域的非神经胶质细胞在调节新陈代谢方面发挥着重要作用。在此,我们概述了目前关于神经内分泌轴调控新陈代谢的教条观点,并更新了这种以神经元为中心的观点,纳入了与神经胶质细胞(包括澹细胞、星形胶质细胞、小胶质细胞和少突胶质细胞系细胞)有关的新证据。我们讨论了神经胶质细胞与激素转运和下丘脑炎症有关的最新研究,强调这些细胞是导致代谢控制和功能障碍的关键因素。因此,神经胶质细胞为未来的治疗设计提供了新的细胞和分子靶点,从而从新的角度解决代谢疾病的治疗问题。
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