Instituto de Investigación, Desarrollo e Innovación en Biotecnología Sanitaria de Elche (IDiBE), Universidad Miguel Hernández, Elche, Spain; Biomedical Research Center in Diabetes and Associated Metabolic Disorders (CIBERDEM), Madrid, Spain; Department of Physiology, Genetics and Microbiology, University of Alicante, Alicante, Spain.
Instituto de Investigación, Desarrollo e Innovación en Biotecnología Sanitaria de Elche (IDiBE), Universidad Miguel Hernández, Elche, Spain; Department of Physiology, Genetics and Microbiology, University of Alicante, Alicante, Spain.
Ageing Res Rev. 2022 Sep;80:101674. doi: 10.1016/j.arr.2022.101674. Epub 2022 Jun 17.
The prevalence of type 2 diabetes (T2D) and impaired glucose tolerance (IGT) increases with ageing. T2D generally results from progressive impairment of the pancreatic islets to adapt β-cell mass and function in the setting of insulin resistance and increased insulin demand. Several studies have shown an age-related decline in peripheral insulin sensitivity. However, a precise understanding of the pancreatic β-cell response in ageing is still lacking. In this review, we summarize the age-related alterations, adaptations and/or failures of β-cells at the molecular, morphological and functional levels in mouse and human. Age-associated alterations include processes such as β-cell proliferation, apoptosis and cell identity that can influence β-cell mass. Age-related changes also affect β-cell function at distinct steps including electrical activity, Ca signaling and insulin secretion, among others. We will consider the potential impact of these alterations and those mediated by senescence pathways on β-cells and their implications in age-related T2D. Finally, given the great diversity of results in the field of β-cell ageing, we will discuss the sources of this heterogeneity. A better understanding of β-cell biology during ageing, particularly at older ages, will improve our insight into the contribution of β-cells to age-associated T2D and may boost new therapeutic strategies.
2 型糖尿病(T2D)和葡萄糖耐量受损(IGT)的患病率随着年龄的增长而增加。T2D 通常是由于胰岛β细胞质量和功能在胰岛素抵抗和胰岛素需求增加的情况下逐渐受损而导致的。几项研究表明,外周胰岛素敏感性随年龄增长而下降。然而,人们对衰老过程中胰岛β细胞的反应仍缺乏精确的理解。在这篇综述中,我们总结了在小鼠和人类中,β细胞在分子、形态和功能水平上与年龄相关的改变、适应和/或衰竭。与年龄相关的改变包括β细胞增殖、凋亡和细胞身份等过程,这些过程会影响β细胞的数量。与年龄相关的变化还会影响β细胞在包括电活动、Ca 信号和胰岛素分泌在内的不同步骤中的功能。我们将考虑这些改变以及衰老途径介导的改变对β细胞的潜在影响及其在与年龄相关的 T2D 中的意义。最后,鉴于β细胞衰老领域的研究结果存在很大的差异,我们将讨论这种异质性的来源。更好地了解衰老过程中β细胞的生物学特性,特别是在老年时,将有助于我们深入了解β细胞对与年龄相关的 T2D 的贡献,并可能促进新的治疗策略的发展。