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抑制脂肪组织 M1 细胞因子表达可降低 2 型糖尿病模型小鼠的 DPP4 活性和胰岛素抵抗。

Inhibiting adipose tissue M1 cytokine expression decreases DPP4 activity and insulin resistance in a type 2 diabetes mellitus mouse model.

机构信息

Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.

Institute of Emergency and Critical Care Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.

出版信息

PLoS One. 2021 May 27;16(5):e0252153. doi: 10.1371/journal.pone.0252153. eCollection 2021.

Abstract

Adipose tissue inflammation is a major cause of the pathogenesis of obesity and comorbidities. To study the involvement of M1/M2 cytokine expression of adipose tissue in the regulatory mechanisms of dipeptidyl peptidase 4 (DPP4) and insulin resistance in diabetes, stromal vascular fractions (SVFs) were purified from inguinal adipose tissue of diabetic (Leprdb/db) and non-diabetic (Lepr+/+) mice followed by analysis of M1/M2 cytokine expression. SVFs of Leprdb/db mice exhibited increased TNF-α, IL-6, IL-1β, CCL2, and DPP4 mRNA expression but decreased IL-10 mRNA expression. Plasma from Leprdb/db mice induced TNF-α, IL-6, IL-1β, CCL2, and DPP4 mRNA expression and plasma from Lepr+/+ mice induced IL-10 mRNA expression in SVFs from Leprdb/db mice. Injection of Lepr+/+ plasma into the adipose tissue of Leprdb/db mice decreased mRNA expression of TNF-α, IL-6, IL-1β, CCL2, and DPP4 and protein expression of pJNK and DPP4 in SVFs, reduced mRNA expression of ICAM, FMO3, IL-1β, iNOS, TNF-α, IL-6, and DPP4 and protein expression of ICAM, FMO3, and DPP4 in liver, and suppressed mRNA expression of TNF-α, IL-6, IL-1β, and DPP4 in Kupffer cells. Plasma from Leprdb/db mice did not induce M1 cytokine expression in SVFs from Leprdb/db-Jnk1-/- mice. Altogether, we demonstrate that diabetes induces M1 but decreases M2 cytokine expression in adipose tissue. Diabetic plasma-induced M1 expression is potentially through pJNK signaling pathways. Non-diabetic plasma reverses M1/M2 cytokine expression, plasma CCL2 levels, DPP4 activity, and Kupffer cell activation in diabetes. Our results suggest M1/M2 cytokine expression in adipose tissue is critical in diabetes-induced DPP4 activity, liver inflammation, and insulin resistance.

摘要

脂肪组织炎症是肥胖和合并症发病机制的主要原因。为了研究二肽基肽酶 4 (DPP4) 和糖尿病胰岛素抵抗调节机制中脂肪组织 M1/M2 细胞因子表达的参与,从糖尿病(Leprdb/db)和非糖尿病(Lepr+/+)小鼠腹股沟脂肪组织中纯化基质血管部分(SVF),然后分析 M1/M2 细胞因子表达。Leprdb/db 小鼠的 SVF 表现出增加的 TNF-α、IL-6、IL-1β、CCL2 和 DPP4 mRNA 表达,但降低的 IL-10 mRNA 表达。Leprdb/db 小鼠的血浆诱导 SVF 中 TNF-α、IL-6、IL-1β、CCL2 和 DPP4 的 mRNA 表达,而 Lepr+/+ 小鼠的血浆诱导 SVF 中 IL-10 mRNA 表达。将 Lepr+/+ 血浆注射到 Leprdb/db 小鼠的脂肪组织中,降低了 SVF 中 TNF-α、IL-6、IL-1β、CCL2 和 DPP4 的 mRNA 表达以及 pJNK 和 DPP4 的蛋白表达,降低了 SVF 中 ICAM、FMO3、IL-1β、iNOS、TNF-α、IL-6 和 DPP4 的 mRNA 表达以及 ICAM、FMO3 和 DPP4 的蛋白表达,并且抑制了 Kupffer 细胞中 TNF-α、IL-6、IL-1β 和 DPP4 的 mRNA 表达。Leprdb/db 小鼠的血浆不能诱导 Leprdb/db-Jnk1-/- 小鼠 SVF 中的 M1 细胞因子表达。总之,我们证明糖尿病诱导脂肪组织中 M1 但降低 M2 细胞因子表达。糖尿病血浆诱导的 M1 表达可能是通过 pJNK 信号通路。非糖尿病血浆逆转糖尿病中 M1/M2 细胞因子表达、血浆 CCL2 水平、DPP4 活性和 Kupffer 细胞激活。我们的结果表明,脂肪组织中 M1/M2 细胞因子表达在糖尿病诱导的 DPP4 活性、肝脏炎症和胰岛素抵抗中至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf1/8158933/4a6fda7291c7/pone.0252153.g001.jpg

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