Zhang Tongran, Wang Nannan, Zhu Lingqiang, Chen Lihua, Liu Huisheng
Guangzhou Laboratory, Guangzhou 510006, China.
Department of Pathophysiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430074, China.
Biomedicines. 2023 Mar 11;11(3):856. doi: 10.3390/biomedicines11030856.
Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) leads to morbidity and mortality, with several clinical manifestations, and has caused a widespread pandemic. It has been found that type 2 diabetes is a risk factor for severe coronavirus disease 2019 (COVID-19) illness. Moreover, accumulating evidence has shown that SARS-CoV-2 infection can increase the risk of hyperglycemia and diabetes, though the underlying mechanism remains unclear because of a lack of authentic disease models to recapitulate the abnormalities involved in the development, regeneration, and function of human pancreatic islets under SARS-CoV-2 infection. Stem-cell-derived islet organoids have been valued as a model to study islets' development and function, and thus provide a promising model for unraveling the mechanisms underlying the onset of diabetes under SARS-CoV-2 infection. This review summarized the latest results from clinical and basic research on SARS-CoV-2-induced pancreatic islet damage and impaired glycemic control. Furthermore, we discuss the potential and perspectives of using human ES/iPS cell-derived islet organoids to unravel the bidirectional relationship between glycemic control and SARS-CoV-2 infection.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染会导致发病和死亡,有多种临床表现,并引发了全球大流行。已发现2型糖尿病是2019冠状病毒病(COVID-19)重症的一个风险因素。此外,越来越多的证据表明,SARS-CoV-2感染会增加高血糖和糖尿病的风险,但其潜在机制仍不清楚,因为缺乏可靠的疾病模型来重现SARS-CoV-2感染下人胰岛发育、再生和功能异常的情况。干细胞来源的胰岛类器官被视为研究胰岛发育和功能的模型,因此为揭示SARS-CoV-2感染下糖尿病发病机制提供了一个有前景的模型。本综述总结了SARS-CoV-2诱导胰岛损伤和血糖控制受损的临床和基础研究的最新结果。此外,我们还讨论了利用人胚胎干细胞/诱导多能干细胞来源的胰岛类器官来揭示血糖控制与SARS-CoV-2感染之间双向关系的潜力和前景。