Isolation of senescent cells by iodixanol (OptiPrep) density gradient-based separation

被引:15
|
作者
Kovacovicova, Kristina [1 ]
Vinciguerra, Manlio [1 ]
机构
[1] Int Clin Res Ctr FNUSA ICRC, Ctr Translat Med, Brno, Czech Republic
关键词
CELLULAR SENESCENCE; IDENTIFICATION; CHEMOTHERAPY; DOXORUBICIN; MECHANISMS;
D O I
10.1111/cpr.12674
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objectives Chemotherapeutic drugs induce senescence in cancer cells but, unlike replicative senescence or oncogene-induced senescence, do so rather inefficiently and depending on DNA damage. A thorough understanding of the biology of chemotherapy-induced senescent cells requires their isolation from a mixed population of adjacent senescent and non-senescent cancer cells. Materials and methods We have developed and optimized a rapid iodixanol (OptiPrep)-based gradient centrifugation system to identify, isolate and characterize doxorubicin (DXR)-induced senescent hepatocellular carcinoma (HCC) cells (HepG2 and Huh-7) in vitro. Results After cellular exposure to DXR, we used iodixanol gradient-based centrifugation to isolate and re-plate cells on collagen-coated flasks, despite their low or null proliferative capacity. The isolated cell populations were enriched for DXR-induced senescent HCC cells, as confirmed by proliferation arrest assay, and beta-galactosidase and DNA damage-dependent gamma H2A.X staining. Conclusions Analysing pure cultures of chemotherapy-induced senescent versus non-responsive cancer cells will increase our knowledge on chemotherapeutic mechanisms of action, and help refine current therapeutic strategies.
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页数:9
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