Foggensteiner L, Bone A J, Webster K A, Wilkin T J
Endocrine Section, Southamptom General Hospital, United Kingdom.
Diabetes. 1990 Oct;39(10):1165-9. doi: 10.2337/diab.39.10.1165.
We recently described autoantibodies that stimulate the release of insulin from pancreatic beta-cells both in vitro and in vivo. The aim of this study was to establish whether islet cell-stimulating antibodies (ICSTAs) also increase islet cell preproinsulin mRNA content. Wistar rat islets, isolated by collagenase digestion, were exposed to 2.7 and 11.1 mM glucose. Insulin release increased 10-fold in response to the higher glucose concentration, and dot-blot analysis of islet mRNA with a rat preproinsulin cDNA probe showed a concomitant increase in mRNA levels. The globulin fractions of four test serums, three from patients with type I (insulin-dependent) diabetes and one from a patient with the insulin autoimmune syndrome, showed clear (5- to 8-fold) stimulation of insulin release. The nonglobulin fractions of these serums and both fractions of three control serums failed to stimulate secretion of insulin. The insulin mRNA content of islets incubated with the ICSTA globulin fractions was greatly increased compared with levels observed in islets treated with control serum globulin fractions. We conclude that ICSTAs not only can stimulate the release of insulin but also increase the preproinsulin mRNA content of islet cells.
我们最近描述了一种自身抗体,该抗体在体外和体内均能刺激胰岛β细胞释放胰岛素。本研究的目的是确定胰岛细胞刺激抗体(ICSTA)是否也会增加胰岛细胞前胰岛素原mRNA的含量。通过胶原酶消化分离得到的Wistar大鼠胰岛,分别暴露于2.7 mM和11.1 mM葡萄糖环境中。在较高葡萄糖浓度刺激下,胰岛素释放增加了10倍,并且用大鼠前胰岛素原cDNA探针进行的胰岛mRNA斑点印迹分析显示mRNA水平同时升高。四种测试血清的球蛋白组分,其中三种来自I型(胰岛素依赖型)糖尿病患者,一种来自胰岛素自身免疫综合征患者,均显示出明显的(5至8倍)胰岛素释放刺激作用。这些血清的非球蛋白组分以及三种对照血清的两种组分均未能刺激胰岛素分泌。与用对照血清球蛋白组分处理的胰岛相比,用ICSTA球蛋白组分孵育的胰岛的胰岛素mRNA含量大大增加。我们得出结论,ICSTA不仅可以刺激胰岛素释放,还能增加胰岛细胞前胰岛素原mRNA的含量。