Shisiwei Jianzhong decoction inhibits the adipogenic differentiation of bone marrow mesenchymal stem cells by downregulating nuclear factor of activated T cells, cytoplasmic 4 in non-severe aplastic anemia.

Wang Jun, Wang Bo, Zhang Yun, Lin Shengyun, W U Liqiang
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Abstract

Objective: To investigate the effect of Shisiwei Jianzhong decoction (, SJD) on non-severe aplastic anemia (NSAA).

Methods: Bone marrow mesenchymal stem cells (BMSCs) were isolated from bone marrow samples of 15 NSAA patients and 3 healthy controls. Cells were treated with gradient concentrations of SJD, and a portion was transfected with a vector overexpressing the nuclear factor of activated T cells, cytoplasmic 4 (NFATC4). Cell viability and apoptosis were detected by cell counting kit-8 and flow cytometry, respectively. After adipogenic differentiation induction, lipid droplet formation in BMSCs was examined by Oil Red O staining. The expression of NFATC4, peroxisome proliferator-activated receptor gamma (PPARG), fatty acid-binding protein 4 (FABP4), peroxisome proliferator-activated receptor-gamma coactivator (PGC-1α), and acetylated PGC-1α was measured by quantitative real-time polymerase chain reaction or Western blot.

Results: SJD significantly increased the viability and decreased the apoptosis of NSAA-derived BMSCs. It also dose-dependently inhibited lipid droplet formation and decreased the expression of PPARG and FABP4 in NSAA-derived BMSCs. NFATC4 expression was higher in patients with NSAA than in healthy controls, and SJD downregulated its expression. NFATC4 overexpression reversed the inhibitory effect of SJD on adipogenic differentiation. Additionally, SJD promoted the deacetylation of PGC-1α in NSAA-derived BMSCs, which was also partially eliminated by NFATC4 overexpression.

Conclusions: SJD inhibits adipogenic differentiation of BMSCs through downregulating NFATC4, thereby contributing to the remission of NSAA.

十四味建中汤通过下调活化T细胞核因子细胞质4抑制非重度再生障碍性贫血骨髓间充质干细胞成脂分化。
目的:探讨四味健中汤对非重度再生障碍性贫血(NSAA)的治疗作用。方法:从15例NSAA患者和3例健康对照者骨髓中分离骨髓间充质干细胞(BMSCs)。用梯度浓度的SJD处理细胞,并用过表达活化T细胞核因子细胞质4 (NFATC4)的载体转染一部分细胞。采用细胞计数试剂盒-8检测细胞活力,流式细胞术检测细胞凋亡。诱导成脂分化后,油红O染色检测骨髓间充质干细胞脂滴形成情况。采用实时定量聚合酶链反应或Western blot检测NFATC4、过氧化物酶体增殖物激活受体γ (PPARG)、脂肪酸结合蛋白4 (FABP4)、过氧化物酶体增殖物激活受体γ辅助激活因子(PGC-1α)和乙酰化PGC-1α的表达。结果:SJD显著提高了nsaa来源的骨髓间充质干细胞的活力,减少了细胞凋亡。它还能剂量依赖性地抑制脂滴形成,降低nsaa来源的骨髓间充质干细胞中PPARG和FABP4的表达。NFATC4在NSAA患者中的表达高于健康对照组,SJD下调其表达。NFATC4过表达逆转了SJD对成脂分化的抑制作用。此外,SJD促进了nsaa来源的BMSCs中PGC-1α的去乙酰化,NFATC4过表达也部分消除了PGC-1α的去乙酰化。结论:SJD通过下调NFATC4抑制骨髓间充质干细胞的成脂分化,从而有助于缓解NSAA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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