枸杞多糖通过 ATF6/SIRT1 依赖性机制改善脂肪组织中脂滴的积聚。

Rui Zhou, Yajing Liu, Weiqiang Hu, Jing Yang, Bing Lin, Zhentian Zhang, Mingyan Chen, Jingwen Yi, Cuifeng Zhu
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引用次数: 0

摘要

脂滴是储存中性脂质的动态细胞器,与肥胖密切相关。以前的研究表明,枸杞多糖(LBP)补充剂可改善肥胖,但其潜在机制仍不清楚。在本研究中,我们假设枸杞多糖通过活化转录因子-6(ATF6)/小分子sirtuin 1(SIRT1)依赖机制抑制脂肪特异性蛋白27(Fsp27),从而减轻脂肪组织(AT)中的低密度脂蛋白积累。高脂饮食(HFD)喂养的小鼠会诱导 AT 中的低密度脂蛋白积累,并诱导 3T3-L1 前脂肪细胞(PA)分化。然后在体内和体外研究了枸杞多糖缓解 LD 累积的能力及其可能的内在机制。此外,还检测了枸杞多糖对 LD 相关基因(ATF6 和 Fsp27)表达的影响。结果表明,HFD 和 PA 分化分别显著增加了 ATs 和脂肪细胞中的 LD 积累,而补充枸杞多糖能明显抑制这些影响。此外,枸杞多糖还能明显激活SIRT1,降低ATF6和Fsp27的表达。有趣的是,当 ATF6 被过表达或沉默时,枸杞多糖的抑制作用分别被取消或加剧。此外,SIRT1 的水平通过 ATF6 介导的相反作用受 LBP 的转录调控。总之,我们的研究结果表明,补充枸杞多糖可通过改善低密度脂蛋白的积累来减轻肥胖,而这可能部分是由 ATF6/SIRT1 依赖性机制介导的。
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Lycium barbarum polysaccharide ameliorates the accumulation of lipid droplets in adipose tissue via an ATF6/SIRT1-dependent mechanism.
Lipid droplets (LDs) are dynamic organelles that store neutral lipids and are closely linked to obesity. Previous studies have suggested that Lycium barbarum polysaccharide (LBP) supplements can ameliorate obesity, but the underlying mechanisms remain unclear. In this study, we hypothesize that LBP alleviates LD accumulation in adipose tissue (AT) by inhibiting fat-specific protein 27 (Fsp27) through an activating transcription factor-6 (ATF6)/small-molecule sirtuin 1 (SIRT1)-dependent mechanism. LD accumulation in AT is induced in high-fat diet (HFD)-fed mice, and differentiation of 3T3-L1 preadipocytes (PAs) is induced. The ability of LBP to alleviate LD accumulation and the possible underlying mechanism are then investigated both in vivo and in vitro. The influences of LBP on the expressions of LD-associated genes ( ATF6 and Fsp27) are also detected. The results show that HFD and PA differentiation markedly increase LD accumulation in ATs and adipocytes, respectively, and these effects are markedly suppressed by LBP supplementation. Furthermore, LBP significantly activates SIRT1 and decreases ATF6 and Fsp27 expressions. Interestingly, the inhibitory effects of LBP are either abolished or exacerbated when ATF6 is overexpressed or silenced, respectively. Furthermore, SIRT1 level is transcriptionally regulated by LBP through opposite actions mediated by ATF6. Collectively, our findings suggest that LBP supplementation alleviates obesity by ameliorating LD accumulation, which might be partially mediated by an ATF6/SIRT1-dependent mechanism.
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