EA 7288, Biocommunication en Cardio-metabolique (BC2M), Faculté de Pharmacie, 15 avenue Charles Flahault, BP 14491, 34093 Montpellier Cedex 5, France.
EA 7288, Biocommunication en Cardio-metabolique (BC2M), Faculté de Pharmacie, 15 avenue Charles Flahault, BP 14491, 34093 Montpellier Cedex 5, France.
Biochim Biophys Acta Mol Basis Dis. 2018 Oct;1864(10):3378-3387. doi: 10.1016/j.bbadis.2018.07.024. Epub 2018 Jul 23.
Inflammatory factors produced and secreted by adipose tissue, in particular peri-pancreatic adipose tissue (P-WAT), may influence pancreatic β-cell dysfunction. Using the ZDF Rat model of diabetes, we show the presence of infiltrating macrophage (ED1 staining) on pancreatic tissue and P-WAT in the pre-diabetes stage of the disease. Then, when the T2D is installed, infiltrating cells decreased. Meanwhile, the P-WAT conditioned-medium composition, in terms of inflammatory factors, varies during the onset of the T2D. Using chemiarray technology, we observed an over expression of CXCL-1, -2, -3, CCL-3/MIP-1α and CXCL-5/LIX and TIMP-1 in the 9 weeks old obese ZDF pre-diabetic rat model. Surprisingly, the expression profile of these factors decreased when animals become diabetic (12 weeks obese ZDF rats). The expression of these inflammatory proteins is highly associated with inflammatory infiltrate. P-WAT conditioned-medium from pre-diabetes rats stimulates insulin secretion, cellular proliferation and apoptosis of INS-1 cells. However, inhibition of conditioned-medium chemokines acting via CXCR2 receptor do not change cellular proliferation apoptosis and insulin secretion of INS-1 cells induced by P-WAT conditioned-medium. Taken together, these results show that among the secreted chemokines, increased expression of CXCL-1, -2, -3 and CXCL-5/LIX in P-WAT conditioned-medium is concomitant with the onset of the T2D but do not exerted a direct effect on pancreatic β-cell dysfunction.
脂肪组织(尤其是胰腺周围脂肪组织[P-WAT])产生和分泌的炎症因子可能会影响胰腺β细胞功能障碍。我们使用 ZDF 糖尿病大鼠模型,显示出在疾病的糖尿病前期阶段,胰腺组织和 P-WAT 存在浸润的巨噬细胞(ED1 染色)。然后,当 T2D 发生时,浸润细胞减少。同时,P-WAT 条件培养基的组成,就炎症因子而言,在 T2D 的发作过程中发生变化。使用 chemiarray 技术,我们观察到在 9 周龄肥胖 ZDF 糖尿病前期大鼠模型中,CXCL-1、-2、-3、CCL-3/MIP-1α 和 CXCL-5/LIX 和 TIMP-1 的表达过度。令人惊讶的是,当动物发生糖尿病(12 周龄肥胖 ZDF 大鼠)时,这些因子的表达谱下降。这些炎症蛋白的表达与炎症浸润高度相关。来自糖尿病前期大鼠的 P-WAT 条件培养基可刺激 INS-1 细胞的胰岛素分泌、细胞增殖和细胞凋亡。然而,通过 CXCR2 受体抑制条件培养基趋化因子的作用并不能改变 P-WAT 条件培养基诱导的 INS-1 细胞的增殖、凋亡和胰岛素分泌。总之,这些结果表明,在分泌的趋化因子中,P-WAT 条件培养基中 CXCL-1、-2、-3 和 CXCL-5/LIX 的表达增加与 T2D 的发生同时发生,但对胰腺β细胞功能障碍没有直接影响。