Md Moin Abu Saleh, Dhawan Sangeeta, Cory Megan, Butler Peter C, Rizza Robert A, Butler Alexandra E
Larry L. Hillblom Islet Research Center (A.S.M.M., S.D., M.C., P.C.B., A.E.B.), David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California; Division of Endocrinology, Diabetes, Metabolism, and Nutrition (R.A.R.), Mayo Clinic College of Medicine, Rochester, MN 55905.
J Clin Endocrinol Metab. 2016 Oct;101(10):3628-3636. doi: 10.1210/jc.2016-2496. Epub 2016 Jul 29.
It has been suggested that beta cell loss in type 2 diabetes (T2D) may be due to beta cell degranulation and/or altered cell identity. While shown to have a minor role in obese T2D, this has not been evaluated in lean T2D.
To establish the contribution of altered beta cell identity in lean T2D and, using a rodent model of lean T2D, whether changes in beta cell identity precede hyperglycemia.
DESIGN, SETTING, AND PARTICIPANTS: We investigated the frequency of chromogranin A positive hormone negative (CPHN) and polyhormonal endocrine cells in pancreas from 10 lean nondiabetic and 10 lean T2D subjects and in pancreas from wild-type and human IAPP transgenic rats at the prediabetic and diabetic stages.
CPHN cells and polyhormonal-expressing cells were comparably increased in lean T2D and human IAPP transgenic rats, in the latter both before and at onset of diabetes. However, the extent of these cells could only account for approximately 2% of beta cell loss.
Degranulation and altered identity play at most a minor role in the beta cell deficit in lean T2D. Because the increase in CPHN and polyhormonal cells precede diabetes onset, these changes are likely a response to stress rather than hyperglycemia, and may reflect attempted regeneration.
有研究表明,2型糖尿病(T2D)中的β细胞丢失可能是由于β细胞脱颗粒和/或细胞身份改变所致。虽然已证明其在肥胖型T2D中作用较小,但在瘦型T2D中尚未进行评估。
确定细胞身份改变在瘦型T2D中的作用,并利用瘦型T2D的啮齿动物模型,研究β细胞身份改变是否先于高血糖出现。
设计、地点和参与者:我们调查了10名瘦型非糖尿病和10名瘦型T2D受试者胰腺中嗜铬粒蛋白A阳性激素阴性(CPHN)细胞和多激素内分泌细胞的频率,以及野生型和人胰岛淀粉样多肽转基因大鼠在糖尿病前期和糖尿病期胰腺中这些细胞的频率。
在瘦型T2D和人胰岛淀粉样多肽转基因大鼠中,CPHN细胞和表达多激素的细胞均有类似增加,在后者中,糖尿病发生前和发病时均如此。然而,这些细胞的数量仅约占β细胞丢失的2%。
脱颗粒和身份改变在瘦型T2D的β细胞缺陷中至多起次要作用。由于CPHN细胞和多激素细胞的增加先于糖尿病发病,这些变化可能是对压力的反应而非高血糖的反应,并且可能反映了尝试性再生。