Department of Infectious Diseases, Ziyang First People's Hospital, Ziyang, China.
Zhejiang Provincial Key Laboratory of Laboratory Animals and Safety Research, Hangzhou Medical College, Hangzhou, China.
Braz J Med Biol Res. 2024 Mar 18;57:e13235. doi: 10.1590/1414-431X2024e13235. eCollection 2024.
The imbalance between pro-inflammatory M1 and anti-inflammatory M2 macrophages plays a critical role in the pathogenesis of sepsis-induced acute lung injury (ALI). Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) may modulate macrophage polarization toward the M2 phenotype by altering mitochondrial activity. This study aimed to investigate the role of the PGC-1α agonist pioglitazone (PGZ) in modulating sepsis-induced ALI. A mouse model of sepsis-induced ALI was established using cecal ligation and puncture (CLP). An in vitro model was created by stimulating MH-S cells with lipopolysaccharide (LPS). qRT-PCR was used to measure mRNA levels of M1 markers iNOS and MHC-II and M2 markers Arg1 and CD206 to evaluate macrophage polarization. Western blotting detected expression of peroxisome proliferator-activated receptor gamma (PPARγ) PGC-1α, and mitochondrial biogenesis proteins NRF1, NRF2, and mtTFA. To assess mitochondrial content and function, reactive oxygen species levels were detected by dihydroethidium staining, and mitochondrial DNA copy number was measured by qRT-PCR. In the CLP-induced ALI mouse model, lung tissues exhibited reduced PGC-1α expression. PGZ treatment rescued PGC-1α expression and alleviated lung injury, as evidenced by decreased lung wet-to-dry weight ratio, pro-inflammatory cytokine secretion (tumor necrosis factor-α, interleukin-1β, interleukin-6), and enhanced M2 macrophage polarization. Mechanistic investigations revealed that PGZ activated the PPARγ/PGC-1α/mitochondrial protection pathway to prevent sepsis-induced ALI by inhibiting M1 macrophage polarization. These results may provide new insights and evidence for developing PGZ as a potential ALI therapy.
促炎型 M1 巨噬细胞和抗炎型 M2 巨噬细胞之间的失衡在脓毒症诱导的急性肺损伤 (ALI) 的发病机制中起着关键作用。过氧化物酶体增殖物激活受体γ共激活因子 1-α(PGC-1α)可以通过改变线粒体活性来调节巨噬细胞向 M2 表型的极化。本研究旨在探讨 PGC-1α 激动剂吡格列酮 (PGZ) 调节脓毒症诱导的 ALI 的作用。采用盲肠结扎和穿孔 (CLP) 建立脓毒症诱导的 ALI 小鼠模型。通过用脂多糖 (LPS) 刺激 MH-S 细胞建立体外模型。使用 qRT-PCR 测量 M1 标志物诱导型一氧化氮合酶 (iNOS) 和主要组织相容性复合体 II (MHC-II) 以及 M2 标志物精氨酸酶 1 (Arg1) 和 CD206 的 mRNA 水平,以评估巨噬细胞极化。Western blot 检测过氧化物酶体增殖物激活受体 γ (PPARγ) PGC-1α 和线粒体生物发生蛋白 NRF1、NRF2 和 mtTFA 的表达。为了评估线粒体含量和功能,通过二氢乙啶染色检测活性氧 (ROS) 水平,并通过 qRT-PCR 测量线粒体 DNA 拷贝数。在 CLP 诱导的 ALI 小鼠模型中,肺组织中 PGC-1α 的表达降低。PGZ 治疗挽救了 PGC-1α 的表达并减轻了肺损伤,这表现在肺湿重/干重比降低、促炎细胞因子(肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-6)分泌减少以及 M2 巨噬细胞极化增强。机制研究表明,PGZ 通过抑制 M1 巨噬细胞极化激活 PPARγ/PGC-1α/线粒体保护途径来预防脓毒症诱导的 ALI。这些结果可能为开发 PGZ 作为潜在的 ALI 治疗方法提供新的见解和证据。