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肌肉源性干细胞/祖细胞功能障碍限制了早衰症小鼠模型的健康寿命和寿命。

Muscle-derived stem/progenitor cell dysfunction limits healthspan and lifespan in a murine progeria model.

机构信息

Stem Cell Research Center, 206 Bridgeside Point II, 450 Technology Drive, Pittsburgh, Pennsylvania 15219, USA.

出版信息

Nat Commun. 2012 Jan 3;3:608. doi: 10.1038/ncomms1611.

Abstract

With ageing, there is a loss of adult stem cell function. However, there is no direct evidence that this has a causal role in ageing-related decline. We tested this using muscle-derived stem/progenitor cells (MDSPCs) in a murine progeria model. Here we show that MDSPCs from old and progeroid mice are defective in proliferation and multilineage differentiation. Intraperitoneal administration of MDSPCs, isolated from young wild-type mice, to progeroid mice confer significant lifespan and healthspan extension. The transplanted MDSPCs improve degenerative changes and vascularization in tissues where donor cells are not detected, suggesting that their therapeutic effect may be mediated by secreted factor(s). Indeed, young wild-type-MDSPCs rescue proliferation and differentiation defects of aged MDSPCs when co-cultured. These results establish that adult stem/progenitor cell dysfunction contributes to ageing-related degeneration and suggests a therapeutic potential of post-natal stem cells to extend health.

摘要

随着年龄的增长,成体干细胞的功能会丧失。然而,目前尚无直接证据表明这是与衰老相关的衰退的因果关系。我们使用鼠类早衰模型中的肌肉源性干细胞/祖细胞(MDSPC)对此进行了测试。在这里,我们表明来自老年和早衰小鼠的 MDSPC 在增殖和多谱系分化方面存在缺陷。将从小鼠中分离的 MDSPC 腹腔内注射到早衰小鼠中,可显著延长其寿命和健康寿命。移植的 MDSPC 可改善组织中的退行性变化和血管生成,而在未检测到供体细胞的地方,这表明它们的治疗效果可能是由分泌因子介导的。事实上,当共培养时,年轻的野生型 MDSPC 可挽救老年 MDSPC 的增殖和分化缺陷。这些结果表明,成体干细胞/祖细胞功能障碍导致与衰老相关的退化,并提示出生后干细胞具有延长健康的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d8/3272577/b36a12b701c9/ncomms1611-f1.jpg

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