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小鼠分化特异性角蛋白1和角蛋白10需要预先存在的角蛋白支架来形成细丝网络。

Mouse differentiation-specific keratins 1 and 10 require a preexisting keratin scaffold to form a filament network.

作者信息

Kartasova T, Roop D R, Holbrook K A, Yuspa S H

机构信息

Laboratory of Cellular Carcinogenesis and Tumor Promotion, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

J Cell Biol. 1993 Mar;120(5):1251-61. doi: 10.1083/jcb.120.5.1251.

Abstract

Keratins 1 (K1) and 10 (K10) are the predominant cytoskeletal intermediate filaments of epidermal cells during transition from the proliferative to the terminal differentiation stage. In situ, formation of the K1/K10 intermediate filament network occurs in the cytoplasm of cells with a preexisting cytoskeleton composed of keratins 5 and 14. To define cytoskeletal interactions permissive for formation of the K1/K10 filamentous network, active copies of mouse K1 and K10 genes were introduced into fibroblasts (NIH 3T3) which do not normally express these proteins. Transient and stable transfectants, as well as heterokaryons produced by fusions with epithelial cells, were evaluated for expression of K1 and K10 proteins and filament formation using specific antibodies. In contrast to keratin pairs K5/K14 and K8/K18, the K1/K10 pair failed to form an extensive keratin filament network on its own, although small isolated dense K1/K10 filament bundles were observed throughout the cytoplasm by EM. K1 and K10 filaments integrated only into the preexisting K5/K14 network upon fusion of the NIH 3T3 (K1/K10) cells with epithelial cells expressing endogenous K5/K14 or with NIH 3T3 cells which were transfected with active copies of the K5 and K14 genes. When combinations of active recombinant gene constructs for keratins 1, 5, 10, and 14 were tested in transient NIH 3T3 transfections, the most intact cytokeratin network observed by immunofluorescence was formed by the K5/K14 pair. The K1/K14 pair was capable of forming a cytoskeletal network, but the network was poorly developed, and usually perinuclear. Transfection of K10 in combination with K5 or K1 resulted in cytoplasmic agglomerates, but not a cytoskeleton. These results suggest that the formation of the suprabasal cytoskeleton in epidermis is dependent on the preexisting basal cell intermediate filament network. Furthermore, restrictions on filament formation appear to be more stringent for K10 than for K1.

摘要

角蛋白1(K1)和角蛋白10(K10)是表皮细胞从增殖阶段过渡到终末分化阶段时主要的细胞骨架中间丝。在原位,K1/K10中间丝网络在具有由角蛋白5和14组成的预先存在的细胞骨架的细胞胞质中形成。为了确定允许形成K1/K10丝状网络的细胞骨架相互作用,将小鼠K1和K10基因的活性拷贝导入通常不表达这些蛋白质的成纤维细胞(NIH 3T3)中。使用特异性抗体评估瞬时和稳定转染子以及与上皮细胞融合产生的异核体中K1和K10蛋白的表达和丝形成情况。与角蛋白对K5/K14和K8/K18不同,K1/K10对自身无法形成广泛的角蛋白丝网络,尽管通过电子显微镜在整个细胞质中观察到了小的孤立致密K1/K10丝束。当NIH 3T3(K1/K10)细胞与表达内源性K5/K14的上皮细胞或与用K5和K14基因的活性拷贝转染的NIH 3T3细胞融合时,K1和K10丝仅整合到预先存在的K5/K14网络中。当在瞬时NIH 3T3转染中测试角蛋白1、5、10和14的活性重组基因构建体组合时,通过免疫荧光观察到的最完整的细胞角蛋白网络是由K5/K14对形成的。K1/K14对能够形成细胞骨架网络,但该网络发育不良,通常位于核周。将K10与K5或KZ组合转染导致细胞质聚集,但未形成细胞骨架。这些结果表明,表皮中基底上层细胞骨架的形成依赖于预先存在的基底细胞中间丝网络。此外,对丝形成的限制似乎对K10比对K1更严格。

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