Section for Cell Biology and Physiology, Department of Biology, University of Copenhagen, Denmark.
Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
J Endocrinol. 2023 Sep 8;259(1). doi: 10.1530/JOE-23-0081. Print 2023 Sep 1.
Since the discovery of glucagon 100 years ago, the hormone and the pancreatic islet alpha cells that produce it have remained enigmatic relative to insulin-producing beta cells. Canonically, alpha cells have been described in the context of glucagon's role in glucose metabolism in liver, with glucose as the primary nutrient signal regulating alpha cell function. However, current data reveal a more holistic model of metabolic signalling, involving glucagon-regulated metabolism of multiple nutrients by the liver and other tissues, including amino acids and lipids, providing reciprocal feedback to regulate glucagon secretion and even alpha cell mass. Here we describe how various nutrients are sensed, transported and metabolised in alpha cells, providing an integrative model for the metabolic regulation of glucagon secretion and action. Importantly, we discuss where these nutrient-sensing pathways intersect to regulate alpha cell function and highlight key areas for future research.
自 100 年前发现胰高血糖素以来,该激素及其产生的胰岛α细胞相对于胰岛素产生的β细胞而言仍然是一个谜。经典上,α细胞一直被描述为在肝脏葡萄糖代谢中胰高血糖素的作用背景下,葡萄糖是调节α细胞功能的主要营养信号。然而,目前的数据揭示了一个更全面的代谢信号模型,涉及到肝脏和其他组织(包括氨基酸和脂质)中胰高血糖素调节的多种营养物质的代谢,为调节胰高血糖素分泌甚至α细胞质量提供了相互反馈。在这里,我们描述了各种营养物质在α细胞中的感知、运输和代谢方式,为胰高血糖素分泌和作用的代谢调节提供了一个综合模型。重要的是,我们讨论了这些营养感应途径在何处交汇以调节α细胞功能,并强调了未来研究的关键领域。