Abstract:OBJECTIVE: To explore the relationship of telomerase RNA component (hTERC) and the telomerase reverse transcriptase (hTERT) with telomerase activity in the marrow hemopoietic stem cells of children with aplastic anemia (AA). METHODS: Fifty-two children with chronic AA, 13 children with acute AA and 21 normal controls were enrolled in the study. Telomerase activity and the expression of mRNA of hTERT and hTERC were detected by Telomeric Repeat Amplification Protocol (TRAP) with silver staining and real-time Q-PCR respectively. RESULTS: Levels of telomerase activity in both the chronic and acute AA groups were higher than in the control group (P<0.01). The AA groups had significantly higher expression of hTERT mRNA than the control group (P<0.01). The chronic AA group had higher expression of hTERT mRNA and telomerase activity than the acute AA group (P<0.05). There was no significant difference in the expression of hTERC mRNA among the three groups (P=0.812). There was a significant correlation between the expression of hTERT mRNA and telomerase activity (r=0.660, P<0.01). CONCLUSIONS: Expression of telomerase activity may be involved in the pathophysiology and development of AA, and hTERT plays a crucial role in expression of telomerase activity.
WANG Xi-Ge,ZHOU Yu-Jie,WANG Dan-Feng et al. Expression of telomerase activity and its related genes in the marrow hemopoietic stem cells of children with aplastic anemia[J]. CJCP, 2013, 15(1): 25-28.
[8]Abdellah BM, Haack-Sorensen M, Burns JS, Elsnab B, Jakob F, Hokland P, et al. Maintenance of differentiation potential of human bone marrow mesenchymal stem cells immoratalized by human telomerase reverse transeriptase gene despite extensive proliferation[J].Biochem Biophys Res Commun, 2005, 326(3): 527-538.
[9]Mitchell JR, Wood E, Collins K. A telomerase component is defective in the human disease dyskeratosis congenital[J]. Nature, 1999, 402(6761): 551-555.
[13]Zhao YM, Li JY, Lan JP, Lai XY, Luo Y, Sun J, et al. Cell cycle dependent telomere regulation by telomerase in human bone marrow mesenchymal stem cells[J]. Biochemi Biophys Res Commu, 2008, 369(4): 1114-1119.
[4]Kamikozuru K, Fukunaga K, Hirota S, Hida N, Ohda Y, Yoshida K, et al. The expression profile of functional regulatory T cells,CD4+CD25high+/forkhead box protein P3+, in patients with ulcerative colitis during active and quiescent disease[J]. Clin Exp Immunol, 2009, 156(2): 320-327.
[5]王西阁,曹祎明,王晓格. CD4+CD25int /highCD127low调节性 T 细胞在再生障碍性贫血患儿中的检测及意义[J].中国当代儿科杂志,2011,13(4): 292-293.
[8]Abdellah BM, Haack-Sorensen M, Burns JS, Elsnab B, Jakob F, Hokland P, et al. Maintenance of differentiation potential of human bone marrow mesenchymal stem cells immoratalized by human telomerase reverse transeriptase gene despite extensive proliferation[J].Biochem Biophys Res Commun, 2005, 326(3): 527-538.
[9]Mitchell JR, Wood E, Collins K. A telomerase component is defective in the human disease dyskeratosis congenital[J]. Nature, 1999, 402(6761): 551-555.
[10]Brummendorf TH, Maciejewski JP, Mak J, Young NS, Lansdorp PM. Telomere length in leukocyte subpopulations of patients with aplastie anemia[J].Blood, 2001, 97(4): 895-900.
[13]Zhao YM, Li JY, Lan JP, Lai XY, Luo Y, Sun J, et al. Cell cycle dependent telomere regulation by telomerase in human bone marrow mesenchymal stem cells[J]. Biochemi Biophys Res Commu, 2008, 369(4): 1114-1119.