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通过荧光激活细胞分选技术分离并鉴定推定的内在多药耐药中国仓鼠卵巢细胞

Isolation and characterization of putative intrinsic multidrug resistant Chinese hamster ovary cells by fluorescence activated cell sorting.

作者信息

Zou C P, Van N T, Kuo M T

机构信息

Department of Molecular Pathology, University of Texas M.D. Anderson Cancer Center, Houston 77030.

出版信息

Anticancer Res. 1992 Mar-Apr;12(2):427-32.

PMID:1349795
Abstract

Most multidrug resistant cell lines reported in the literature were established by long-term continuous exposure of cells to stepwise increasing concentrations of antitumor drugs. However, these resistant cell lines may not be relevant to the majority of clinically resistant cells. In this study, we described the establishment of doxorubicin (Dox)-resistant Chinese hamster ovary cells by repeated flow cytometric cell sorting using the intrinsic fluorescence of Dox. In each sorting, the 15% least fluorescent cells were fractionated, grown to mass culture and sorted again. Results from a total of nine sorting cycles showed that the intracellular levels of Dox in the sorted cells were inversely proportional to the number of sorting cycles. The levels of P-glycoprotein mRNA in the sorted cells were increased, but reached a plateau of 2-3 fold after the fifth sorting cycle. The sorted cells exhibited a moderate but stable multidrug-resistant phenotype. Because the procedure involved minimal exposure of cells to the drug, the isolated cells are most likely related to naturally occurring (intrinsic) MDR cells.

摘要

文献中报道的大多数多药耐药细胞系是通过将细胞长期连续暴露于逐步增加浓度的抗肿瘤药物而建立的。然而,这些耐药细胞系可能与大多数临床耐药细胞无关。在本研究中,我们描述了通过利用阿霉素(Dox)的固有荧光进行重复流式细胞术细胞分选来建立阿霉素耐药的中国仓鼠卵巢细胞。在每次分选中,分选荧光最弱的15%的细胞,培养至大规模培养后再次分选。总共九个分选周期的结果表明,分选细胞中阿霉素的细胞内水平与分选周期数成反比。分选细胞中P-糖蛋白mRNA水平升高,但在第五个分选周期后达到2至3倍的平台期。分选细胞表现出中等但稳定的多药耐药表型。由于该过程涉及细胞与药物的最小暴露,分离出的细胞很可能与天然存在的(内在的)多药耐药细胞有关。

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