Effect of various oxygen concentrations on biological function of human bone marrow hematopoietic stem/progenitor cells.
- Author:
Yi-Wen HAO
1
;
Da-Ye CHENG
;
Wen-Ling ZHOU
;
Yi-Ran MA
;
Yu-Ting WANG
Author Information
1. Department of Blood Transfusion, China Medical University First Hospital, Shenyang, 110001, Liaoning Province, China. hyw82666@163.com
- Publication Type:Journal Article
- MeSH:
Bone Marrow Cells;
cytology;
drug effects;
Bone Marrow Transplantation;
Cell Hypoxia;
Cells, Cultured;
Hematopoietic Stem Cell Transplantation;
Hematopoietic Stem Cells;
cytology;
drug effects;
Humans;
Oxygen;
administration & dosage;
pharmacology
- From:
Journal of Experimental Hematology
2010;18(4):997-1001
- CountryChina
- Language:Chinese
-
Abstract:
Hypoxia in bone marrow is suitable for the perfect preservation of biological functions of bone marrow hematopoietic stem cells (BM HSC). It is deserved to study whether the biological functions of BM HSC are influenced when being exposed to environment of oxygen at various concentration during amplification of BM HSCs in normal oxygen condition in vitro and process of peripheral blood hematopoietic stem cell transplantation (PBSCT). This study was purposed to investigate the effects of various oxygen concentrations on biological functions of human BM HSCs. The BM HSCs were amplified in vitro, the amplification level of CD34(+) HSCs and CD34(+)AC133(+) HSCs were detected by flow cytometry, the apoptosis and cell cycle distribution of CD34(+) HSCs amplified in various oxygen concentrations were assayed by flow cytometry with Annexin V/PI double staining as well as PI and Ki-67 antibody, respectively, the differentiation of amplified CD34(+) HSCs in vitro was determined by direction differentiation assay, the migration ability of amplified CD34(+)AC133(+) HSCs was measured by migration test. The results indicated that the oxygen environment below normal oxygen, especially hypoxia, could amplify more primitive CD34(+)AC133(+) HSCs and CD34(+) HSCs with activity, arrest more HSCs in G₀/G₁ phase, promote the generation of BFU-E, CFU-GM, CFU-GEMM, and better preserve the migration ability of HSCs. While the above functional indicators of BM HSCs were poor when HSCs exposed to normoxia, oxygen-unstable and oxygen-severe changeable environments. It is concluded that the biological functions of BM HSCs in PBSCT are related with oxygen concentration and its stability, the culture of BM HSCs in lower oxygen environment may be more beneficial for PBSCT.
