Bourlon P M, Faure-Dussert A, Billaudel B, Sutter B C, Tramu G, Thomasset M
Laboratoire Endocrinologie, Université Bordeaux I, Talence, France.
J Endocrinol. 1996 Feb;148(2):223-32. doi: 10.1677/joe.0.1480223.
The pancreatic B cell is equipped with specific receptors for 1,25-dihydroxyvitamin D3 (1,25-(OH)2D3) and contains vitamin D-dependent calcium binding proteins (calbindin-D). Insulin secretion is impaired by vitamin D deficiency and is restored by 1,25-(OH)2D3 (concomitantly with an improved calcium handling within B cells) but the effect of 1,25-(OH)2D3 on the pancreatic B cell via calbindin-D is unclear. Therefore we examined the relationship between calbindin-D28K or calbindin-D9K and the activity of the endocrine pancreas in normal (N), four week vitamin D-deficient (-D) and one week 1,25-(OH)2D3-replete (+D) rats. Calbindin-D9K was not found in the pancreas, neither in the islets nor in the exocrine part, of any of the groups of rats (N, -D, or+D). Surprisingly, total islet calbindin-D28K content was increased by vitamin D deficiency and partly restored by 1,25-(OH)2D3. Calbindin-D28K immunostaining was observed only on A and B cells in the endocrine part of the pancreas, the greatest staining being found in A cells. This difference in staining density was increased by vitamin D deficiency and decreased by 1,25-(OH)2D3 treatment. In vitro, 1,25-(OH)2D3 also produced a negative influence on calbindin-D28K staining in A cells, as demonstrated using pieces of pancreas incubated with the steroid for 2 h. No significant influence on labeling intensity of B cell calbindin-D28K could be shown. Plasma insulin and islet insulin release in response to 10 mM arginine stimulation were decreased in -D rats and enhanced in +D rats towards N values. In contrast, plasma glucagon and the amount of glucagon secretion, stimulated in vitro by 10 mM arginine or by low (1.7 mM) glucose concentration, was increased in -D rats and attenuated by 1,25-(OH)2D3. Thus there appears to be no relationship between the steady state level of B cell calbindin-D28K and the regulation of insulin secretion by 1,25-(OH)2D3 in vitamin D-deficient rats. However there is a correlation between A cell calbindin-D28K and glucagon secretion, which are both negatively regulated by 1,25-(OH)2D3. The predominance of calbindin-D28K in A cells raises the question as to how A and B cells interact and the role of calbindin-D28K in calcium handling.
胰腺β细胞具有1,25 - 二羟基维生素D3(1,25-(OH)2D3)的特异性受体,并含有维生素D依赖性钙结合蛋白(钙结合蛋白-D)。维生素D缺乏会损害胰岛素分泌,而1,25-(OH)2D3可使其恢复(同时β细胞内的钙处理得到改善),但1,25-(OH)2D3通过钙结合蛋白-D对胰腺β细胞的作用尚不清楚。因此,我们研究了正常(N)、维生素D缺乏4周(-D)和1,25-(OH)2D3补充1周(+D)大鼠中钙结合蛋白-D28K或钙结合蛋白-D9K与内分泌胰腺活性之间的关系。在任何一组大鼠(N、-D或+D)的胰腺中,无论是胰岛还是外分泌部分,均未发现钙结合蛋白-D9K。令人惊讶的是,维生素D缺乏会使胰岛总钙结合蛋白-D28K含量增加,而1,25-(OH)2D3可使其部分恢复。钙结合蛋白-D28K免疫染色仅在胰腺内分泌部分的A细胞和B细胞上观察到,A细胞中的染色最强。这种染色密度的差异在维生素D缺乏时增加,而在1,25-(OH)2D3处理后降低。在体外,如用与该类固醇孵育2小时的胰腺切片所示,1,25-(OH)2D3对A细胞中的钙结合蛋白-D28K染色也有负面影响。未显示对B细胞钙结合蛋白-D28K标记强度有显著影响。-D大鼠对10 mM精氨酸刺激的血浆胰岛素和胰岛胰岛素释放减少,而+D大鼠则向N值增强。相反,-D大鼠中由10 mM精氨酸或低(1.7 mM)葡萄糖浓度体外刺激的血浆胰高血糖素和胰高血糖素分泌量增加,而1,25-(OH)2D3可使其减弱。因此,在维生素D缺乏的大鼠中,β细胞钙结合蛋白-D28K的稳态水平与1,25-(OH)2D3对胰岛素分泌的调节之间似乎没有关系。然而,A细胞钙结合蛋白-D28K与胰高血糖素分泌之间存在相关性,二者均受1,25-(OH)2D3的负调节。A细胞中钙结合蛋白-D28K的优势地位引发了关于A细胞和B细胞如何相互作用以及钙结合蛋白-D28K在钙处理中的作用的问题。