Anaerobic Glycolysis and HIF1α Expression in Haematopoietic Stem Cells Explains Its Quiescence Nature.

Q4 Biochemistry, Genetics and Molecular Biology
Journal of Stem Cells Pub Date : 2015-01-01
Lokanathan Srikanth, Manne Mudhu Sunitha, Katari Venkatesh, Pasupuleti Santhosh Kumar, Chodimella Chandrasekhar, Bhuma Vengamma, Potukuchi Venkata Gurunadha Krishna Sarma
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Abstract

Metabolic alteration that a stem cell undergoes during proliferation and quiescence are decisive. These cells survive in extreme hypoxic environment that prevails in bone marrow. The present study is aimed to understand this nature in hematopoietic stem cells. These stem cells were mobilized from bone marrow into peripheral blood by giving G-CSF at a concentration of 5 μg/Kg/d and the cells were isolated by apheresis technique. The morphological analysis of these cells using Giemsa stain and SEM showed presence of only single type of cells with conspicuous nuclei, the hematopoietic nature was assessed by the presence of CD34, a glycoprotein using anti-CD34 monoclonal antibodies. The ICC results revealed presence of CD34 marker further; pure population of CD34+ stem cells was described by FACS. These cells were cultured separately in DMEM having 5.5mM, 11.1mM and 25mM glucose respectively. In these cells GK, PK and L-LDH enzyme activities were estimated which showed increased activities at 5.5mM glucose concentration and further elevation of glucose concentration the activities were fallen considerably. Similarly, qPCR analysis of HIF1α and GAPDH genes showed very high expression of HIF1α at 5.5mM glucose concentration which reduced with increased glucose concentration. While GAPDH gene expression enhanced on elevation of glucose concentration. Thus, these results indicate high HIF1α expression in low glucose condition with improved anaerobic glycolysis seems to be one of the key factors in maintaining the quiescent state of CD34+ stem cells.

造血干细胞的无氧糖酵解和HIF1α表达解释其休眠性质。
干细胞在增殖和静止期间所经历的代谢改变是决定性的。这些细胞在骨髓中普遍存在的极度缺氧环境中存活。本研究旨在了解造血干细胞的这种性质。用浓度为5 μg/Kg/d的G-CSF将这些干细胞从骨髓中动员到外周血中,并采用离心分离法分离细胞。利用吉氏染色和扫描电镜对这些细胞进行形态学分析,发现只有一种类型的细胞具有明显的细胞核,使用抗CD34单克隆抗体通过CD34(一种糖蛋白)的存在来评估造血性质。ICC结果进一步显示CD34标记的存在;用流式细胞仪描述CD34+干细胞的纯群体。将这些细胞分别培养在含5.5mM、11.1mM和25mM葡萄糖的DMEM中。测定细胞中GK、PK和L-LDH酶活性,葡萄糖浓度为5.5mM时活性升高,葡萄糖浓度进一步升高后活性明显下降。同样,对HIF1α和GAPDH基因的qPCR分析显示,在5.5mM葡萄糖浓度下,HIF1α的表达量非常高,并随着葡萄糖浓度的增加而降低。GAPDH基因表达随葡萄糖浓度升高而增强。因此,这些结果表明,在低糖条件下高表达HIF1α并改善厌氧糖酵解可能是维持CD34+干细胞静止状态的关键因素之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Stem Cells
Journal of Stem Cells Medicine-Transplantation
CiteScore
0.10
自引率
0.00%
发文量
1
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