Léon Stéphane, Nadjar Agnès, Quarta Carmelo
Neurocentre Magendie, Physiopathologie de la Plasticité Neuronale, INSERM U1215, University of Bordeaux, 33000 Bordeaux, France.
Int J Mol Sci. 2021 May 15;22(10):5243. doi: 10.3390/ijms22105243.
Diet-induced obesity can originate from the dysregulated activity of hypothalamic neuronal circuits, which are critical for the regulation of body weight and food intake. The exact mechanisms underlying such neuronal defects are not yet fully understood, but a maladaptive cross-talk between neurons and surrounding microglial is likely to be a contributing factor. Functional and anatomical connections between microglia and hypothalamic neuronal cells are at the core of how the brain orchestrates changes in the body's metabolic needs. However, such a melodious interaction may become maladaptive in response to prolonged diet-induced metabolic stress, thereby causing overfeeding, body weight gain, and systemic metabolic perturbations. From this perspective, we critically discuss emerging molecular and cellular underpinnings of microglia-neuron communication in the hypothalamic neuronal circuits implicated in energy balance regulation. We explore whether changes in this intercellular dialogue induced by metabolic stress may serve as a protective neuronal mechanism or contribute to disease establishment and progression. Our analysis provides a framework for future mechanistic studies that will facilitate progress into both the etiology and treatments of metabolic disorders.
饮食诱导的肥胖可能源于下丘脑神经回路的活动失调,而下丘脑神经回路对体重和食物摄入的调节至关重要。这种神经元缺陷的确切机制尚未完全明确,但神经元与周围小胶质细胞之间的适应性不良相互作用可能是一个促成因素。小胶质细胞与下丘脑神经元细胞之间的功能和解剖学联系是大脑协调身体代谢需求变化的核心。然而,这种和谐的相互作用可能会因长期饮食诱导的代谢应激而变得适应性不良,从而导致过度进食、体重增加和全身代谢紊乱。从这个角度出发,我们批判性地讨论了参与能量平衡调节的下丘脑神经回路中小胶质细胞 - 神经元通讯的新兴分子和细胞基础。我们探讨了由代谢应激引起的这种细胞间对话的变化是可能作为一种保护性神经元机制,还是会导致疾病的发生和进展。我们的分析为未来的机制研究提供了一个框架,这将有助于推进对代谢紊乱的病因学和治疗方法的研究。