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Rb家族蛋白在上皮发育过程中对不同细胞谱系进行差异性调控。

Rb family proteins differentially regulate distinct cell lineages during epithelial development.

作者信息

Wikenheiser-Brokamp Kathryn A

机构信息

Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA.

出版信息

Development. 2004 Sep;131(17):4299-310. doi: 10.1242/dev.01232. Epub 2004 Aug 4.

Abstract

pRb, p107 and p130 are important regulators of cell cycle and have extensive overlapping functions; however, only Rb has been shown to be a bone fide tumor suppressor. Defining the overlapping versus distinct pocket protein functions is therefore an important step to understanding the unique role of Rb. Using lung as a model, the present studies demonstrate that pocket proteins are important not only in regulating cell cycle and survival but also in cell lineage specification. An inducible lung-specific Rb knockout strategy was used to demonstrate that Rb is specifically required for restricting neuroendocrine cell fate despite functional compensation for Rb deficiency in other cell types. Ablation of total Rb family function resulted in opposing effects in specification along distinct cell lineages, providing evidence that pocket proteins inhibit neuroendocrine cell fate while being required for differentiation in other cell types. These findings identify a novel role for pocket proteins in cell fate determination, and establish a unique cell lineage-specific function for Rb that explains, at least in part, why Rb and p16 are inactivated in phenotypically distinct carcinomas.

摘要

视网膜母细胞瘤蛋白(pRb)、p107和p130是细胞周期的重要调节因子,具有广泛的重叠功能;然而,只有Rb被证明是一种真正的肿瘤抑制因子。因此,明确口袋蛋白的重叠功能与独特功能是理解Rb独特作用的重要一步。以肺为模型,本研究表明口袋蛋白不仅在调节细胞周期和细胞存活方面很重要,而且在细胞谱系特化中也很重要。采用诱导性肺特异性Rb基因敲除策略来证明,尽管其他细胞类型对Rb缺陷有功能补偿,但Rb对于限制神经内分泌细胞命运是特别必需的。完全敲除Rb家族功能在不同细胞谱系的特化中产生了相反的效应,这表明口袋蛋白抑制神经内分泌细胞命运,而在其他细胞类型的分化中是必需的。这些发现确定了口袋蛋白在细胞命运决定中的新作用,并为Rb建立了独特的细胞谱系特异性功能(这至少部分解释了为什么Rb和p16在表型不同的癌症中失活)。

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