Alpha-cells: Its Role as the Islet Harmonizer

N. K. Elnaggar, M. N. Elnaggar
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Abstract

It has long been thought that the alpha cells and its secretory products play an important role solely in maintaining euglycemia and preventing hypoglycemia through a contradictory action to the B cell’s insulin. The α-cell function is tightly regulated by various physiological inputs including systemic energy status, central and autonomic nervous systems, and the endocrine system. It is also an important amino acid sensor, glucagon blockade suppresses hepatic amino acid catabolism and increases the serum amino acid level. In addition to those controllers, the intra-islet microenvironment, where α-cells are located, has been recently revealed to be important in the regulation of the various cellular secretory functions including the overlapping of glucagon and insulin secretion through a precise cell-cell crosstalk. Paracrine interactions between pancreatic islet cells have been proposed as a mechanism to regulate hormone secretion and glucose homeostasis, alpha and B cells are closely positioned on the sides of their blood supply where acetylcholine acts as the paracrine communicator of signals inside the islets. Recently, it has been demonstrated that blocking acetylcholine esterase increases insulin secretion. Moreover, it has also been suggested that glucagon is not exclusively a counter-regulatory hormone that elevates blood glucose levels, in contrast it can cause hypoglycemia conditioned by the presence of intact B cells and a functional GLP-1R (glucagon-like peptide 1 receptor). These data argue for glucagon agonism in modern management of T2DM. Alpha-cells also, have been shown to be able to trans-differentiate into β-cells only in the presence of insulin-positive cells with α-cell origin in the lineage tracing analyses, confirming the role of α-cells as a source of β-cell regeneration. The article reviews the updated knowledge about the functions of the alpha-cells and its role in the paracrine control of islet cell secretions and the future therapeutic potentials.
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α细胞:作为胰岛协调者的角色
长期以来,人们一直认为α细胞及其分泌产物仅通过与B细胞的胰岛素相矛盾的作用,在维持血糖和预防低血糖中起重要作用。α-细胞的功能受到全身能量状态、中枢和自主神经系统、内分泌系统等多种生理输入的严格调控。胰高血糖素阻断可抑制肝脏氨基酸分解代谢,提高血清氨基酸水平。除了这些控制者外,最近发现α-细胞所在的胰岛内微环境在各种细胞分泌功能的调节中起重要作用,包括通过精确的细胞间串扰调节胰高血糖素和胰岛素分泌的重叠。胰岛细胞之间的旁分泌相互作用被认为是调节激素分泌和葡萄糖稳态的一种机制,α细胞和B细胞紧密地位于其血液供应的两侧,其中乙酰胆碱充当胰岛内信号的旁分泌通讯器。最近有研究表明,阻断乙酰胆碱酯酶可增加胰岛素分泌。此外,也有研究表明,胰高血糖素并不仅仅是一种提高血糖水平的反调节激素,相反,它可以引起低血糖,这是由完整的B细胞和功能性GLP-1R(胰高血糖素样肽1受体)的存在所决定的。这些数据支持胰高血糖素激动剂在现代T2DM治疗中的应用。在谱系追踪分析中,α-细胞也被证明只有在α-细胞来源的胰岛素阳性细胞存在时才能转化为β-细胞,这证实了α-细胞作为β-细胞再生来源的作用。本文综述了关于α -细胞的功能及其在胰岛细胞分泌旁分泌控制中的作用和未来治疗潜力的最新知识。
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