Expression of microRNA-451 in normal and thalassemic erythropoiesis

被引:51
作者
Svasti, Saovaros [2 ,3 ]
Masaki, Shizuka [1 ]
Penglong, Tipparat [2 ]
Abe, Yasunobu [4 ]
Winichagoon, Pranee [2 ]
Fucharoen, Suthat [2 ]
Umemura, Tsukuru [1 ]
机构
[1] Kyushu Univ, Dept Hlth Sci, Fac Med Sci, Higashi Ku, Fukuoka 8128582, Japan
[2] Mahidol Univ, Thalassemia Res Ctr, Inst Mol Biosci, Salaya, Nakornpathom, Thailand
[3] Mahidol Univ, Dept Biochem, Fac Sci, Bangkok 10700, Thailand
[4] Kyushu Univ, Fac Med Sci, Fukuoka 812, Japan
基金
日本学术振兴会;
关键词
Thalassemia; miRNA; Erythropoiesis; BETA-THALASSEMIA; ERYTHROID-DIFFERENTIATION; CANCER-CELLS; APOPTOSIS; GENE; PRECURSORS; DIAGNOSIS; MIR-451; RNAS;
D O I
10.1007/s00277-010-0980-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
MicroRNAs (miRNAs) are negative regulators of gene expression that play an important role in hematopoiesis. Thalassemia, a defective globin synthesis leading to precipitate of excess unbound globins in red blood cell precursors, results in defective erythroid precursors and ineffective erythropoiesis. Expression pattern of miR-451, an erythroid-specific miRNA, was analyzed during differentiation of erythroid progenitors derived from normal and thalassemic peripheral blood CD34-positive cells, after 14 days of culture. A biphasic expression with transient up-regulation of miRNA-451 on day 3 of cultures was observed during thalassemic erythroid differentiation. In contrast, the expression pattern of the miR-451 in erythroid cells obtained from the other extravascular hemolytic anemia, i.e., hereditary spherocytosis patients showed no transient up-regulation of miR-451 on day 3 of cultures. Our results suggest that early erythroid progenitors in beta-thalassemia have a dysregulated miRNA-451 expression program, and analysis of microRNA is a relevant approach to determine abnormalities of erythropoiesis.
引用
收藏
页码:953 / 958
页数:6
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