Acidic stress induced G1 cell cycle arrest and intrinsic apoptotic pathway in Jurkat T-lymphocytes

被引:6
|
作者
Kim, Jee Young [1 ]
Cheng, Xinlai [1 ]
Woelfl, Stefan [1 ]
机构
[1] Heidelberg Univ, Inst Pharm & Mol Biotechnol, Pharmaceut Biol, Neuenheimer Feld 364, D-69120 Heidelberg, Germany
关键词
Jurkat T-Iymphocyte; Acidic stress; Apoptosis; Caspase-9; G1; phase; Alkaline phosphatase (AP); ACUTE LYMPHOBLASTIC-LEUKEMIA; ALKALINE-PHOSPHATASE ACTIVITY; INTRACELLULAR PH; CANCER-THERAPY; GROWTH; MICROENVIRONMENT; DIFFERENTIATION; ENVIRONMENTS; FIBROBLASTS; MODULATION;
D O I
10.1016/j.yexcr.2016.11.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Low extracellular pH (pH(e)) is a common hallmark of tumor microenvironment, which will also affect pH sensitive T-lymphocytes in this environment. Due to the growing interest on T-cell mediated cancer therapies, acidic stress induced consequences on this lymphocyte deserves through investigations. Results: In line with our previous study [Kim et al., Biochem. Biophys. Res. Commun. 2016; 472(4): 585-91.], we applied sub-lethal acidic stress (pH 3.3, 37 C for 25 min) to Jurkat T-lymphocytes. Progression from early apoptosis into late apoptosis was clearly observed by flow cytometry within 3 days. Treatment led to onset of G1 arrest in the first 24 h and cell cycling data corresponded to survival of an invasive alkaline phosphatase (AP) positive population. Concerning the massive cell death observed after 72 h, both mRNA level (qRT-PCR) and protein level (western blotting) data indicate programmed cell death through p53-p21 independent signaling. Conclusion: Taken together, the results obtained suggest that the majority of Jurkat cells exposed to short but intense acidic stress conditions, as used here, undergo intrinsic apoptosis, while invasion and AP activation only occurred in a small surviving cell population.
引用
收藏
页码:140 / 146
页数:7
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