Li Xihong, Qu Yi, Mao Meng, Yu Fan, Li Qiang, Hua Yimin, Mu Dezhi
Department of Pediatrics, West China Second University Hospital, Sichuan University, Sichuan, China.
Transfusion. 2008 Aug;48(8):1627-33. doi: 10.1111/j.1537-2995.2008.01724.x. Epub 2008 May 2.
Normal stem cells usually express a low level of telomerase activity that serves to stabilize the chromosomes during cell division and helps prevent cell senescence. Human telomerase reverse transcriptase (hTERT) is a rate-limiting enzyme that dictates the activity of human telomerase and thus decides the life span of cells. The expression of hTERT and its roles in beta-thalassemia major are unclear, however.
hTERT mRNA expression in bone marrow (BM) CD34+ cells from 25 children with beta-thalassemia major and 15 control subjects was investigated using real-time reverse transcription polymerase chain reaction (RT-PCR) analysis. The serum erythropoietin (sEPO) and hemoglobin (Hb) levels in peripheral blood were also determined. The relationship between hTERT and sEPO as well as Hb was then examined.
It was found that hTERT mRNA expression was significantly up regulated in BM CD34+ cells from patients with beta-thalassemia major. Furthermore, a significantly positive correlation was found between hTERT mRNA and sEPO (r = 0.771, p < 0.001). A significantly inverse correlation, however, was found between hTERT mRNA and Hb concentration (r = -0.929, p < 0.001).
Our findings suggest that severe anemia with low Hb concentration might up regulate hTERT expression of BM CD34+ cells and sEPO levels in patients with beta-thalassemia major.
正常干细胞通常表达低水平的端粒酶活性,该活性在细胞分裂过程中稳定染色体并有助于防止细胞衰老。人端粒酶逆转录酶(hTERT)是一种限速酶,它决定人端粒酶的活性,从而决定细胞的寿命。然而,hTERT在重型β地中海贫血中的表达及其作用尚不清楚。
采用实时逆转录聚合酶链反应(RT-PCR)分析,研究25例重型β地中海贫血患儿和15例对照者骨髓(BM)CD34+细胞中hTERT mRNA的表达。同时测定外周血血清促红细胞生成素(sEPO)和血红蛋白(Hb)水平。然后检测hTERT与sEPO以及Hb之间的关系。
发现重型β地中海贫血患者骨髓CD34+细胞中hTERT mRNA表达显著上调。此外,hTERT mRNA与sEPO之间存在显著正相关(r = 0.771,p < 0.001)。然而,hTERT mRNA与Hb浓度之间存在显著负相关(r = -0.929,p < 0.001)。
我们的研究结果表明,低Hb浓度的严重贫血可能上调重型β地中海贫血患者骨髓CD34+细胞的hTERT表达和sEPO水平。