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细胞周期蛋白依赖性激酶抑制剂p16INK4a修饰的干细胞衰老

Stem-cell ageing modified by the cyclin-dependent kinase inhibitor p16INK4a.

作者信息

Janzen Viktor, Forkert Randolf, Fleming Heather E, Saito Yoriko, Waring Michael T, Dombkowski David M, Cheng Tao, DePinho Ronald A, Sharpless Norman E, Scadden David T

机构信息

Center for Regenerative Medicine, Massachusetts General Hospital, Harvard Medical School, 185 Cambridge Street, Boston, Massachusetts 02114, USA.

出版信息

Nature. 2006 Sep 28;443(7110):421-6. doi: 10.1038/nature05159. Epub 2006 Sep 6.

Abstract

Stem-cell ageing is thought to contribute to altered tissue maintenance and repair. Older humans experience increased bone marrow failure and poorer haematologic tolerance of cytotoxic injury. Haematopoietic stem cells (HSCs) in older mice have decreased per-cell repopulating activity, self-renewal and homing abilities, myeloid skewing of differentiation, and increased apoptosis with stress. Here we report that the cyclin-dependent kinase inhibitor p16INK4a, the level of which was previously noted to increase in other cell types with age, accumulates and modulates specific age-associated HSC functions. Notably, in the absence of p16INK4a, HSC repopulating defects and apoptosis were mitigated, improving the stress tolerance of cells and the survival of animals in successive transplants, a stem-cell-autonomous tissue regeneration model. Inhibition of p16INK4a may ameliorate the physiological impact of ageing on stem cells and thereby improve injury repair in aged tissue.

摘要

干细胞衰老被认为会导致组织维持和修复功能改变。年长的人类骨髓衰竭增加,对细胞毒性损伤的血液学耐受性较差。老年小鼠的造血干细胞(HSC)单细胞再增殖活性、自我更新和归巢能力下降,分化出现髓系偏向,应激时细胞凋亡增加。我们在此报告,细胞周期蛋白依赖性激酶抑制剂p16INK4a,其水平此前已被注意到会随着年龄增长在其他细胞类型中升高,它会积累并调节特定的与年龄相关的造血干细胞功能。值得注意的是,在没有p16INK4a的情况下,造血干细胞再增殖缺陷和细胞凋亡得到缓解,提高了细胞的应激耐受性以及动物在连续移植(一种干细胞自主组织再生模型)中的存活率。抑制p16INK4a可能会改善衰老对干细胞的生理影响,从而改善老年组织中的损伤修复。

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