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外肽酶氨肽酶N/CD13和二肽基肽酶IV/CD26的表达模式:不同类型培养细胞上的免疫超微结构定位

Expression patterns of the ectopeptidases aminopeptidase N/CD13 and dipeptidyl peptidase IV/CD26: immunoultrastructural topographic localization on different types of cultured cells.

作者信息

Stange T, Kettmann U, Holzhausen H J, Riemann D

机构信息

Department of Otorhinolaryngology, Medical School, University of Halle, Germany.

出版信息

Acta Histochem. 1998 Apr;100(2):157-69. doi: 10.1016/s0065-1281(98)80024-x.

Abstract

Aminopeptidase N/CD13 and dipeptidyl peptidase IV/CD26 are widespread membrane-bound peptidases involved in fundamental biological processes. Using cryo-ultramicrotomy of cultured cells followed by indirect immunogold labelling, both enzymes appeared to be strongly and regularly labelled on the cell surfaces of human synovial fibroblasts, T-lymphocytes and colon carcinoma cells Caco-2. In the cytoplasm of the synovial fibroblasts gold-labelled vesicle-like structures were found, which we consider to be potential transport vesicles. An abundant and regular expression of CD13 was detected on cultured renal parenchymal cells. On the renal carcinoma cell line Caki-1 cells we found a low, non-homogeneous and clustered CD13-labelling. On cultured renal parenchymal cells and the Caki-1 cells CD26 could not be observed. The expression pattern of CD26 on renal carcinoma cell line Caki-2 cells showed also a slightly clustered distribution. A low density CD26-labelling was present on the squamous cell carcinoma cell line UM-SCC-22B. CD13 was absent in Caki-2 and UM-SCC-22B cells. The presence of both enzymes on the cultured cells enables their ultrastructural investigation under different growth conditions and their involvement in cell-cell interactions. For this purpose, however, further investigations are necessary.

摘要

氨肽酶N/CD13和二肽基肽酶IV/CD26是广泛存在的膜结合肽酶,参与基本的生物学过程。通过对培养细胞进行冷冻超薄切片,然后进行间接免疫金标记,在人滑膜成纤维细胞、T淋巴细胞和结肠癌细胞Caco-2的细胞表面,这两种酶均呈现出强烈且规则的标记。在滑膜成纤维细胞的细胞质中发现了金标记的囊泡样结构,我们认为这是潜在的转运囊泡。在培养的肾实质细胞上检测到CD13丰富且规则的表达。在肾癌细胞系Caki-1细胞上,我们发现CD13标记较低、不均匀且呈簇状。在培养的肾实质细胞和Caki-1细胞上未观察到CD26。肾癌细胞系Caki-2细胞上CD26的表达模式也显示出略有簇状分布。在鳞状细胞癌细胞系UM-SCC-22B上存在低密度的CD26标记。Caki-2和UM-SCC-22B细胞中不存在CD13。培养细胞上这两种酶的存在使得能够在不同生长条件下对其进行超微结构研究,并研究它们在细胞间相互作用中的作用。然而,为此目的还需要进一步研究。

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