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正常血糖和糖尿病NOD小鼠胰岛中生长抑素受体亚型1-5的表达

Expression of somatostatin receptor subtypes 1-5 in pancreatic islets of normoglycaemic and diabetic NOD mice.

作者信息

Ludvigsen E, Stridsberg M, Janson E T, Sandler S

机构信息

Department of Medical Cell Biology, Uppsala, Sweden.

出版信息

Eur J Endocrinol. 2005 Sep;153(3):445-54. doi: 10.1530/eje.1.01986.

Abstract

OBJECTIVE

Somatostatin acts on five specific receptors (sst1-5) to elicit different biological functions. The non-obese diabetic (NOD) mouse is an experimental model of type 1 diabetes. The aim of this study was to investigate whether the islet expression of sst1-5 is affected during the development of diabetes in NOD mice, with insulitis accompanied by spontaneous hyperglycaemia.

METHODS

By immunostaining for sst1-5 the expression and co-expression together with the four major islet hormones in pancreatic islets were investigated in female and male NOD mice at different stages of disease. The NOD related non-diabetic ICR mouse was also examined.

RESULTS

The islet cells of diabetic NOD mice showed an increased islet cell expression of sst2-5 compared with normoglycaemic female NOD mice. This correlated to increasing age and extent of insulitis. Major findings from the co-expression investigations were that sst2 was expressed in a majority of beta-cells in the normoglycaemic NOD mice, but absent in the beta-cells in the diabetic NOD mice. A majority of the alpha-cells expressed sst2 and 5 in normoglycaemic and diabetic NOD mice. About 60% of delta-cells showed co-expression of sst4 and 5 in both normoglycaemic and diabetic NOD mice. 60% of pancreatic polypeptide (PP)-cells expressed sst4 in both groups. Insulitis was found to be accompanied by a down-regulation of sst in normoglycaemic animals.

CONCLUSIONS

The difference in sst expression in the islets cells of diabetic mice may suggest either a contributing factor in the process leading to diabetes, or a defence response against ongoing beta-cell destruction.

摘要

目的

生长抑素作用于五种特定受体(sst1 - 5)以引发不同的生物学功能。非肥胖糖尿病(NOD)小鼠是1型糖尿病的实验模型。本研究的目的是调查在伴有自发性高血糖的胰岛炎的NOD小鼠糖尿病发展过程中,sst1 - 5在胰岛中的表达是否受到影响。

方法

通过对sst1 - 5进行免疫染色,研究了处于疾病不同阶段的雌性和雄性NOD小鼠胰岛中sst1 - 5的表达及共表达情况,同时还检测了与NOD相关的非糖尿病ICR小鼠。

结果

与血糖正常的雌性NOD小鼠相比,糖尿病NOD小鼠的胰岛细胞中sst2 - 5的胰岛细胞表达增加。这与年龄增长和胰岛炎程度相关。共表达研究的主要发现是,血糖正常的NOD小鼠中大多数β细胞表达sst2,但糖尿病NOD小鼠的β细胞中不存在sst2表达。在血糖正常和糖尿病的NOD小鼠中,大多数α细胞表达sst2和5。在血糖正常和糖尿病的NOD小鼠中,约60%的δ细胞显示sst4和5共表达。两组中60%的胰多肽(PP)细胞表达sst4。发现在血糖正常的动物中,胰岛炎伴随着sst的下调。

结论

糖尿病小鼠胰岛细胞中sst表达的差异可能表明其要么是导致糖尿病过程中的一个促成因素,要么是针对正在进行的β细胞破坏的一种防御反应。

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