Kim Nayoun, Kim Seolsong, Park Seokjae, Kim Eun-Kyoung
Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology, Daegu, Republic of Korea.
Neurometabolomics Research Center, Daegu Gyeongbuk Institute of Science and Technology, Daegu, Republic of Korea.
Exp Mol Med. 2025 May 2. doi: 10.1038/s12276-025-01449-6.
Tanycytes are a pivotal component of the hypothalamic network that controls energy homeostasis. Despite their importance, the regulatory mechanisms governing tanycyte-neuron interactions in response to metabolic signals remain unexplored. Here we report that adenosine signaling between tanycytes and AGRP/NPY neurons is crucial for tanycytic metabolic regulation mediated by translocator protein 18 kDa (TSPO). Tanycyte-specific Tspo-knockout mice displayed reduced food consumption and weight loss associated with the downregulation of Agrp and Npy expression under high-fat diet feeding. Tspo-deficient tanycytes had elevated levels of intracellular ATP, which was released via connexin 43 hemichannels and extracellularly converted into adenosine by tanycytic ectonucleotidases. The adenosine signal was perceived by adenosine A1 receptors on adjacent AGRP/NPY neurons, reducing ERK phosphorylation, which in turn downregulated Agrp and Npy expression. Our findings underscore the anorexic role of adenosine as a gliotransmitter in the intricate communication between tanycytes and neurons for regulating appetite and body weight.
伸展细胞是控制能量平衡的下丘脑网络的关键组成部分。尽管它们很重要,但响应代谢信号时伸展细胞与神经元相互作用的调控机制仍未得到探索。在此,我们报告伸展细胞与促肾上腺皮质激素释放激素/神经肽Y(AGRP/NPY)神经元之间的腺苷信号传导对于由18 kDa转位蛋白(TSPO)介导的伸展细胞代谢调节至关重要。在高脂饮食喂养下,伸展细胞特异性Tspo基因敲除小鼠表现出食物摄入量减少和体重减轻,这与Agrp和Npy表达下调有关。Tspo缺陷的伸展细胞细胞内ATP水平升高,ATP通过连接蛋白43半通道释放,并由伸展细胞外核苷酸酶在细胞外转化为腺苷。腺苷信号被相邻AGRP/NPY神经元上的腺苷A1受体感知,从而减少细胞外信号调节激酶(ERK)磷酸化,进而下调Agrp和Npy表达。我们的研究结果强调了腺苷作为一种胶质递质在伸展细胞与神经元之间调节食欲和体重的复杂通讯中所起的厌食作用。