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敲低 ANGPTL-4 可抑制高糖培养条件下肾小球系膜细胞的炎症反应和细胞外基质积聚。

Knockdown of ANGPTL-4 inhibits inflammatory response and extracellular matrix accumulation in glomerular mesangial cells cultured under high glucose condition.

机构信息

a Department of Nephrology, Huaihe Hospital of Henan University , Kaifeng , P.R. China.

出版信息

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):3368-3373. doi: 10.1080/21691401.2019.1649274.

DOI:10.1080/21691401.2019.1649274
PMID:31387395
Abstract

Diabetic nephropathy (DN) is one of the major diabetic complications that lead to end-stage renal failure. Angiopoietin-like protein-4 (ANGPTL-4) has been reported to be dysregulated in diabetes mellitus and diabetic complications. However, the role of ANGPTL-4 in glomerular mesangial cells (MCs) during DN remains unclear. In the present study, we evaluated the role of ANGPTL-4 in MCs in response to high glucose (HG) condition and the potential mechanism. The results proved that ANGPTL-4 expression is significantly increased in HG-stimulated MCs. Knockdown of ANGPTL-4 suppressed HG-induced cell proliferation of MCs. The production of pro-inflammatory cytokines including TNF-α, IL-1β, IL-6 were decreased in ANGPTL-4 knocked down MCs. Inhibition of ANGPTL-4 markedly suppressed the expressions of extracellular matrix (ECM) proteins, collagen IV (Col IV) and fibronectin (FN), in HG-stimulated MCs. Furthermore, ANGPTL-4 knockdown inhibited the HG-induced activation of NF-κB signaling pathway in MCs. Collectively, knockdown of ANGPTL-4 suppressed HG-induced cell proliferation, inflammatory response, and ECM accumulation inhibiting NF-κB signaling pathway in MCs. These findings suggested that ANGPTL-4 might be a therapeutic target for the prevention and treatment of DN.

摘要

糖尿病肾病 (DN) 是导致终末期肾衰竭的主要糖尿病并发症之一。血管生成素样蛋白 4 (ANGPTL-4) 在糖尿病和糖尿病并发症中被报道失调。然而,ANGPTL-4 在糖尿病肾病肾小球系膜细胞 (MC) 中的作用尚不清楚。在本研究中,我们评估了 ANGPTL-4 在高糖 (HG) 刺激的 MCs 中的作用及其潜在机制。结果证明,HG 刺激的 MCs 中 ANGPTL-4 的表达显著增加。ANGPTL-4 的敲低抑制了 HG 诱导的 MCs 增殖。在 ANGPTL-4 敲低的 MCs 中,促炎细胞因子 TNF-α、IL-1β 和 IL-6 的产生减少。ANGPTL-4 的抑制显著抑制了 HG 刺激的 MCs 中细胞外基质 (ECM) 蛋白胶原 IV (Col IV) 和纤维连接蛋白 (FN) 的表达。此外,ANGPTL-4 的敲低抑制了 HG 诱导的 MCs 中 NF-κB 信号通路的激活。综上所述,ANGPTL-4 的敲低抑制了 HG 诱导的 MCs 增殖、炎症反应和 ECM 积累,抑制了 NF-κB 信号通路。这些发现表明,ANGPTL-4 可能是预防和治疗糖尿病肾病的治疗靶点。

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