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CD68在非髓样细胞类型中的表达。

Expression of CD68 in non-myeloid cell types.

作者信息

Gottfried E, Kunz-Schughart L A, Weber A, Rehli M, Peuker A, Müller A, Kastenberger M, Brockhoff G, Andreesen R, Kreutz M

机构信息

Department of Hematology and Oncology, University of Regensburg, Regensburg, Germany.

出版信息

Scand J Immunol. 2008 May;67(5):453-63. doi: 10.1111/j.1365-3083.2008.02091.x.

Abstract

CD68, the human homologue of macrosialin, is commonly regarded as a selective marker for human monocytes and macrophages. Its expression is thought to be regulated by a macrophage-specific promoter. However, several immunohistochemical studies have indicated that CD68 antibodies also react with other haematopoietic and non-haematopoietic cell types. We investigated the expression of CD68 in various primary cells and carcinoma cell lines using immunohistochemistry, flow cytometry, Western blot analysis and qRT-PCR. Weak but significant immunoreactivity was detected in lymphocytes and several tumour cell lines whereas staining of primary fibroblasts and endothelial cells was comparable to macrophages. The intensity of CD68 staining in individual cell types depended on the antibody clone and the fixation technique. Anti-CD68 mAb KP1 should be used with great caution for frozen tissue sections due to its reactivity with a wide variety of cell types. Also, care should be taken when distinguishing macrophages from fibroblasts/stromal cells in paraffin sections after formalin fixation since both cell types are stained highly positive for CD68. In accordance, mRNA expression of CD68 was not only detected in macrophages and monocytes but also in fibroblasts as well as endothelial cells and tumour cells, although with a varying intensity. Cloning of full length 5'-sequences and determination of transcription start sites shows that macrophages and fibroblasts initiate transcription within the known promoter region; however, from different start sites, indicating alternative promoter architecture in myeloid versus non-myeloid cells. We suggest that CD68 is not a selective macrophage marker but rather a lysosomal protein that is enriched in macrophages.

摘要

CD68是巨噬细胞涎酸蛋白的人类同源物,通常被视为人类单核细胞和巨噬细胞的选择性标志物。其表达被认为受巨噬细胞特异性启动子调控。然而,多项免疫组织化学研究表明,CD68抗体也与其他造血和非造血细胞类型发生反应。我们使用免疫组织化学、流式细胞术、蛋白质免疫印迹分析和定量逆转录聚合酶链反应研究了CD68在各种原代细胞和癌细胞系中的表达。在淋巴细胞和几种肿瘤细胞系中检测到微弱但显著的免疫反应性,而原代成纤维细胞和内皮细胞的染色与巨噬细胞相当。单个细胞类型中CD68染色的强度取决于抗体克隆和固定技术。由于抗CD68单克隆抗体KP1与多种细胞类型有反应性,因此在冷冻组织切片中应极其谨慎使用。此外,在福尔马林固定后的石蜡切片中区分巨噬细胞与成纤维细胞/基质细胞时应小心,因为这两种细胞类型对CD68的染色均呈强阳性。相应地,虽然强度不同,但CD68的mRNA表达不仅在巨噬细胞和单核细胞中检测到,在成纤维细胞、内皮细胞和肿瘤细胞中也检测到。全长5'序列的克隆和转录起始位点的确定表明,巨噬细胞和成纤维细胞在已知启动子区域内启动转录;然而,起始位点不同,表明髓样细胞与非髓样细胞中存在不同的启动子结构。我们认为,CD68不是一种选择性巨噬细胞标志物,而是一种在巨噬细胞中富集的溶酶体蛋白。

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