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利用人白血病细胞系和健康供体外周血细胞建立和评估用于检测多药耐药P-糖蛋白低表达的MRK16-磁性细胞分选试验

Establishment and evaluation of MRK16-magnetic cell sorting assays for detecting low expression of multidrug resistance P-glycoprotein using human leukemia cell lines and peripheral blood cells from healthy donors.

作者信息

Okochi E, Iwahashi T, Ariyoshi K, Watabe H, Tsuruo T, Ono K

机构信息

Pharma Research and Development Division, Hoechst, Japan Ltd., Saitama, Japan.

出版信息

J Immunol Methods. 1995 Nov 16;187(1):127-37. doi: 10.1016/0022-1759(95)00177-c.

DOI:10.1016/0022-1759(95)00177-c
PMID:7490449
Abstract

Two types of magnetic cell sorting assays, termed MRK16-MACS and MRK16-MACS-FACS, have been established to detect low expression level of P-glycoprotein (P-gp) using a monoclonal antibody MRK16, which recognizes a cell surface epitope of P-gp. With K-562 and U-937 cell lines, which are known to express low levels of P-gp and hence routinely used as negative control cell lines in conventional flow cytometry, both assays gave significantly positive reactivities indicating improved specificity and sensitivity of these assays. The findings in the dilution test, where P-gp-positive cells were added to P-gp-negative cells at various ratios, demonstrated that the MRK16-MACS assay is quantitative and capable of detecting small numbers of P-gp-positive cells as few as 2.5% of the total cells tested. Furthermore, specific enrichment of P-gp-expressing cells in magnetic cell sorting assays was verified by reverse transcription-polymerase chain reaction (RT-PCR) analysis and functional assay for P-gp with Rhodamine 123. The availability of such magnetic cell sorting assays may offer an approach to quantitate low level of P-gp expression.

摘要

已建立两种类型的磁性细胞分选检测方法,分别称为MRK16-MACS和MRK16-MACS-FACS,以使用单克隆抗体MRK16检测P-糖蛋白(P-gp)的低表达水平,该抗体识别P-gp的细胞表面表位。对于已知表达低水平P-gp并因此在传统流式细胞术中常规用作阴性对照细胞系的K-562和U-937细胞系,两种检测方法均给出了显著的阳性反应,表明这些检测方法的特异性和灵敏度有所提高。在稀释试验中,将P-gp阳性细胞以不同比例添加到P-gp阴性细胞中,结果表明MRK16-MACS检测方法是定量的,能够检测低至所检测总细胞数2.5%的少量P-gp阳性细胞。此外,通过逆转录聚合酶链反应(RT-PCR)分析和使用罗丹明123的P-gp功能检测,验证了磁性细胞分选检测中P-gp表达细胞的特异性富集。这种磁性细胞分选检测方法的可用性可能为定量低水平P-gp表达提供一种途径。

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