Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Institute of Emergency and Critical Care Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
PLoS One. 2021 May 27;16(5):e0252153. doi: 10.1371/journal.pone.0252153. eCollection 2021.
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.
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。