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首页> 外文期刊>Experimental Gerontology >Bariatric surgery and diet-induced long-term caloric restriction protect subcutaneous adipose-derived stromal/progenitor cells and prolong their life span in formerly obese humans
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Bariatric surgery and diet-induced long-term caloric restriction protect subcutaneous adipose-derived stromal/progenitor cells and prolong their life span in formerly obese humans

机译:减肥手术和饮食诱导的长期热量限制可保护皮下脂肪来源的基质/祖细胞并延长其在先前肥胖人群中的寿命

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摘要

A key effect of prolonged reducing diets and bariatric surgeries in formerly obese people is long-term caloric restriction (CR). The analysis of the impact of these interventions on specific tissues will contribute to a better understanding of their mechanisms of action. The physiological functions of subcutaneous white adipose tissues are mainly fulfilled by adipocytes arising out of adipose-derived stromal/progenitor cells (ASCs), which are crucial for adipose tissue homeostasis. In the present study we analyzed ASC from age-matched long-term calorically restricted formerly obese (CRD), obese (OD) and normal weight donors (NWDs). We demonstrate that ASC derived from CRD has a significant longer replicative lifespan than ASC isolated from OD and NWD. This correlated with strongly reduced DNA-damage and improved survival of the CRD ASC, both are hallmarks of CR. The adipogenic capacity was significantly lower in ASC derived from CRD than that from OD, as shown by reduced expression of the adipogenic key regulator PPAR72 and the differentiation marker FABP4. The adipogenic capacity of ASCs from CRD and NWD differed only slightly. In conclusion, we provide evidence that bariatric surgery and diet-induced long-term CR substantially reprogram ASCs in formerly obese humans, comprising reduced DNA-damage, improved viability, extended replicative lifespan and reduced adipogenic differentiation potential.
机译:长期减少饮食和肥胖手术对以前肥胖的人的关键作用是长期热量限制(CR)。这些干预措施对特定组织的影响的分析将有助于更好地了解其作用机理。皮下白色脂肪组织的生理功能主要由源自脂肪的基质/祖细胞(ASC)产生的脂肪细胞来实现,脂肪细胞对脂肪组织的动态平衡至关重要。在本研究中,我们从年龄匹配的长期热量受限的先前肥胖者(CRD),肥胖者(OD)和正常体重供者(NWD)中分析了ASC。我们证明,从CRD衍生的ASC比从OD和NWD分离的ASC具有更长的复制寿命。这与大大降低的DNA损伤和CRD ASC的存活率提高有关,两者都是CR的标志。脂肪形成关键调节因子PPAR72和分化标记FABP4的表达降低表明,来自CRD的ASC的脂肪形成能力明显低于来自OD的脂肪形成能力。来自CRD和NWD的ASC的脂肪形成能力仅略有不同。总之,我们提供的证据表明,减肥手术和饮食引起的长期CR可以大大重编程以前肥胖的人的ASC,包括减少DNA损伤,提高生存能力,延长复制寿命和降低成脂分化潜能。

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