Impact of apoptotic adipose-derived mesenchymal stem cells on attenuating organ damage and reducing mortality in Rat sepsis syndrome induced by cecal puncture and ligation

脂肪组织 医学 败血症 细胞凋亡 间充质干细胞 炎症 免疫学 内科学 氧化应激 肿瘤坏死因子α 结扎 内分泌学 男科 病理 生物 生物化学
作者
Chia‐Lo Chang,Steve Leu,Hsin‐Ching Sung,Yen‐Yi Zhen,Chung-Lung Cho,Angela Chen,Tzu‐Hsien Tsai,Sheng‐Ying Chung,Han‐Tan Chai,Cheuk‐Kwan Sun,Chia‐Hung Yen,Hon‐Kan Yip
出处
期刊:Journal of Translational Medicine [BioMed Central]
卷期号:10 (1) 被引量:118
标识
DOI:10.1186/1479-5876-10-244
摘要

Abstract Background We tested whether apoptotic adipose-derived mesenchymal stem cells (A-ADMSCs) were superior to healthy (H)-ADMSCs at attenuating organ damage and mortality in sepsis syndrome following cecal ligation and puncture (CLP). Methods Adult male rats were categorized into group 1 (sham control), group 2 (CLP), group 3 [CLP + H-ADMSC administered 0.5, 6, and 18 h after CLP], group 4 [CLP + A-ADMSC administered as per group 3]. Results Circulating peak TNF-α level, at 6 h, was highest in groups 2 and 3, and higher in group 4 than group 1 (p < 0.0001). Immune reactivity (indicated by circulating and splenic helper-, cytoxic-, and regulatory-T cells) at 24 and 72 h exhibited the same pattern as TNF-α amongst the groups (all p < 0.0001). The mononuclear-cell early and late apoptosis level and organ damage parameters of liver (AST, ALT), kidney (creatinine) and lung (arterial oxygen saturation) also displayed a similar pattern to TNF-α levels (all p < 0.001). Protein levels of inflammatory (TNF-α, MMP-9, NF-κB, ICAM-1), oxidative (oxidized protein) and apoptotic (Bax, caspase-3, PARP) biomarkers were higher in groups 2 and 3 than group 1, whereas anti-apoptotic (Bcl-2) biomarker was lower in groups 2 and 3 than in group 1 but anti-oxidant (GR, GPx, HO-1, NQO-1) showed an opposite way of Bcl-2; these patterns were reversed for group 4 (all p < 0.001). Mortality was highest in group 3 and higher in group 2 than group 4 than group 1 (all p < 0.001). Conclusions A-ADMSC therapy protected major organs from damage and improved prognosis in rats with sepsis syndrome.
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