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区分单层与复层鳞状上皮的单克隆细胞角蛋白抗体:对人体组织的特性研究

Monoclonal cytokeratin antibodies that distinguish simple from stratified squamous epithelia: characterization on human tissues.

作者信息

Debus E, Weber K, Osborn M

出版信息

EMBO J. 1982;1(12):1641-7. doi: 10.1002/j.1460-2075.1982.tb01367.x.

DOI:10.1002/j.1460-2075.1982.tb01367.x
PMID:6202511
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC553263/
Abstract

Four monoclonal antibodies designated CK1 - CK4 were obtained from fusions of mouse myeloma F0 cells with spleen cells from BALB/c mice immunized with cytoskeletal preparations made by treatment of human HeLa cells with non-ionic detergents. These IgG1 type antibodies all recognize, in immune blots, cytokeratin 18 (45 kd, pI 5.7) in the catalogue of 19 human cytokeratin species developed by Moll et al. (1982). Immunofluorescence microscopy on human material shows that CK1 - CK4 stain a wide variety of simple epithelia (e.g., intestine, respiratory and urinary systems, liver, glandular epithelia) but do not stain stratified squamous epithelia (e.g., oesophagus, epidermis) or non-epithelial cells. The immunofluorescence results, developed mainly by gel electrophoresis, support the concept of cytokeratin divergence in different epithelia and clarify, for cytokeratin 18, some unsolved problems posed by high tissue complexity. CK2 appears specific for human, CK1 and CK3 for primates, while CK4 shows broad cross-species reactivity. Thus, CK1 - CK4 appear to be valuable tools for cytokeratin typing and initial experiments also suggest that they can be used to further subdivide human tumours of epithelial origin.

摘要

通过将小鼠骨髓瘤F0细胞与用非离子去污剂处理人HeLa细胞制成的细胞骨架制剂免疫的BALB/c小鼠的脾细胞进行融合,获得了四种单克隆抗体,命名为CK1 - CK4。在免疫印迹中,这些IgG1型抗体均能识别Moll等人(1982年)建立的19种人细胞角蛋白目录中的细胞角蛋白18(45kd,pI 5.7)。对人体材料进行免疫荧光显微镜检查显示,CK1 - CK4可对多种单层上皮(如肠道、呼吸系统和泌尿系统、肝脏、腺上皮)进行染色,但不能对复层鳞状上皮(如食道、表皮)或非上皮细胞进行染色。主要通过凝胶电泳得出的免疫荧光结果支持了不同上皮中细胞角蛋白分化的概念,并阐明了细胞角蛋白18在高度复杂组织中存在的一些未解决问题。CK2似乎对人类具有特异性,CK1和CK3对灵长类动物具有特异性,而CK4具有广泛的跨物种反应性。因此,CK1 - CK4似乎是细胞角蛋白分型的有价值工具,初步实验也表明它们可用于进一步细分人上皮源性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/be354c7529f8/emboj00304-0165-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/eaaa27f032e7/emboj00304-0161-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/7d947d6d6992/emboj00304-0162-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/ead767fb9653/emboj00304-0163-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/be354c7529f8/emboj00304-0165-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/eaaa27f032e7/emboj00304-0161-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/7d947d6d6992/emboj00304-0162-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/ead767fb9653/emboj00304-0163-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c020/553263/be354c7529f8/emboj00304-0165-a.jpg

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