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Regulation of metabolic homeostasis by the TGF‐β superfamily receptor ALK7

生物 受体 信号转导 核受体 生物信息学 细胞生物学 遗传学 基因 转录因子
作者
Carlos F. Ibáñez
出处
期刊:FEBS Journal [Wiley]
卷期号:289 (19): 5776-5797 被引量:13
标识
DOI:10.1111/febs.16090
摘要

ALK7 (Activin receptor‐like kinase 7) is a member of the TGF‐β receptor superfamily predominantly expressed by cells and tissues involved in endocrine functions, such as neurons of the hypothalamus and pituitary, pancreatic β‐cells and adipocytes. Recent studies have begun to delineate the processes regulated by ALK7 in these tissues and how these become integrated with the homeostatic regulation of mammalian metabolism. The picture emerging indicates that ALK7’s primary function in metabolic regulation is to limit catabolic activities and preserve energy. Aside of the hypothalamic arcuate nucleus, the function of ALK7 elsewhere in the brain, particularly in the cerebellum, where it is abundantly expressed, remains to be elucidated. Although our understanding of the basic molecular events underlying ALK7 signaling has benefited from the vast knowledge available on TGF‐β receptor mechanisms, how these connect to the physiological functions regulated by ALK7 in different cell types is still incompletely understood. Findings of missense and nonsense variants in the Acvr1c gene, encoding ALK7, of some mouse strains and human subjects indicate a tolerance to ALK7 loss of function. Recent discoveries suggest that specific inhibitors of ALK7 may have therapeutic applications in obesity and metabolic syndrome without overt adverse effects.
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