Oregon Stem Cell Center, Papé Family Pediatric Research Institute, Department of Pediatrics, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, Oregon 97239, USA.
Department of Genetics and Institute for Diabetes, Obesity, and Metabolism; University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Nat Commun. 2016 Jul 11;7:11756. doi: 10.1038/ncomms11756.
Human pancreatic islets of Langerhans contain five distinct endocrine cell types, each producing a characteristic hormone. The dysfunction or loss of the insulin-producing β cells causes diabetes mellitus, a disease that harms millions. Until now, β cells were generally regarded as a single, homogenous cell population. Here we identify four antigenically distinct subtypes of human β cells, which we refer to as β1-4, and which are distinguished by differential expression of ST8SIA1 and CD9. These subpopulations are always present in normal adult islets and have diverse gene expression profiles and distinct basal and glucose-stimulated insulin secretion. Importantly, the β cell subtype distribution is profoundly altered in type 2 diabetes. These data suggest that this antigenically defined β cell heterogeneity is functionally and likely medically relevant.
人类胰岛中的 Langerhans 包含五种不同的内分泌细胞类型,每种细胞都能产生一种特征性激素。胰岛素产生细胞(β 细胞)的功能障碍或丧失会导致糖尿病,这种疾病危害着数百万人的健康。直到现在,β 细胞通常被认为是一种单一的、同质的细胞群体。在这里,我们鉴定出了四种抗原上不同的人类β细胞亚型,我们称之为β1-4,它们通过 ST8SIA1 和 CD9 的差异表达来区分。这些亚群在正常成年胰岛中始终存在,具有不同的基因表达谱和不同的基础和葡萄糖刺激的胰岛素分泌。重要的是,2 型糖尿病患者β细胞亚型的分布发生了深刻的改变。这些数据表明,这种抗原定义的β细胞异质性在功能上可能具有重要意义。