Suppr超能文献

细胞周期抑制剂p21和p16是调节雪旺细胞增殖所必需的。

Cell cycle inhibitors p21 and p16 are required for the regulation of Schwann cell proliferation.

作者信息

Atanasoski Suzana, Boller Danielle, De Ventura Lukas, Koegel Heidi, Boentert Matthias, Young Peter, Werner Sabine, Suter Ueli

机构信息

Department of Biology, Institute of Cell Biology, Swiss Federal Institute of Technology, ETH-Hönggerberg, Zurich, Switzerland.

出版信息

Glia. 2006 Jan 15;53(2):147-57. doi: 10.1002/glia.20263.

Abstract

Regulated cell proliferation is a crucial prerequisite for Schwann cells to achieve myelination in development and regeneration. In the present study, we have investigated the function of the cell cycle inhibitors p21 and p16 as potential regulators of Schwann cell proliferation, using p21- or p16-deficient mice. We report that both inhibitors are required for proper withdrawal of Schwann cells from the cell cycle during development and following injury. Postnatal Schwann cells express p21 exclusively in the cytoplasm, first detectable at postnatal day 7. This cytoplasmic p21 expression is necessary for proper Schwann cell proliferation control in the late development of peripheral nerves. After axonal damage, p21 is found in Schwann cell nuclei during the initiation of the proliferation period. This stage is critically regulated by p21, since loss of p21 leads to a strong increase in Schwann cell proliferation. Unexpectedly, p21 levels are upregulated in this phase suggesting that the role of p21 may be more complex than purely inhibitory for the Schwann cell cycle. However, inhibition of Schwann cell proliferation is the overriding crucial function of p21 and p16 in peripheral nerves as revealed by the consequences of loss-of-function in development and after injury. Different mechanisms appear to underlie the inhibitory function, depending on whether p21 is cytoplasmic or nuclear.

摘要

受调控的细胞增殖是施万细胞在发育和再生过程中实现髓鞘形成的关键前提条件。在本研究中,我们利用p21或p16基因缺失的小鼠,研究了细胞周期抑制剂p21和p16作为施万细胞增殖潜在调节因子的功能。我们报告称,在发育过程中和损伤后,施万细胞从细胞周期中正常退出都需要这两种抑制剂。出生后的施万细胞仅在细胞质中表达p21,最早在出生后第7天可检测到。这种细胞质中的p21表达对于外周神经后期发育中施万细胞增殖的正常控制是必要的。轴突损伤后,在增殖期开始时,施万细胞核中可发现p21。这一阶段受到p21的严格调控,因为p21缺失会导致施万细胞增殖大幅增加。出乎意料的是,此阶段p21水平上调,这表明p21的作用可能比单纯抑制施万细胞周期更为复杂。然而,发育过程中和损伤后功能丧失的后果表明,抑制施万细胞增殖是p21和p16在外周神经中的首要关键功能。根据p21是在细胞质还是细胞核中,不同的机制似乎是其抑制功能的基础。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验