Megakaryocytic differentiation of CD133+ hematopoietic stem cells by down-regulation of microRNA-10a

被引：20

作者：

Zarif, M. Nikougoftar ^{[1
]}

Soleimani, M. ^{[2
]}

Abolghasemi, H. ^{[1
]}

Amirizade, N. ^{[1
]}

Arefian, E. ^{[3
]}

Rahimian, A. ^{[3
]}

机构：

[1] High Inst Res & Educ Transfus Med, Blood Transfus Res Ctr, Tehran, Iran

[2] Tarbiat Modares Univ, Dept Hematol, Sch Med Sci, Tehran 14115331, Iran

[3] Stem Cell Technol Res Ctr, Dept Mol Biol & Genet Engn, Tehran, Iran

来源：

HEMATOLOGY | 2013年 / 18卷 / 02期

关键词：

MicroRNA-10a; Megakaryocyte differentiation; CD133+cells; HOXA1; CORD BLOOD-CELLS; EXPRESSION; MECHANISMS; PATTERNS; GENOME; WORLD;

D O I：

10.1179/1607845412Y.0000000047

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

MicroRNAs (miRNA), as a class of non-coding RNAs, play a crucial role in normal hematopoiesis. Recent studies on miRNA profiling during hematopoiesis showed miR-10a down-regulation in megakaryocytic differentiation. Here we investigated whether decrease in miR-10a can differentiate umbilical cord blood CD133+ cells to megakaryocytic series. We ectopically induced miR-10a down-regulation by locked nucleic acid anti-miR-10a transfection of CD133+ cells. The megakaryocytic differentiation was evaluated by CD42/CD61 and CD41 surface expression and colonogenic capacity in Megacult media. In addition, real-time polymerase chain reaction was done for detection of miR-10a and its target HoxA1 mRNA. HOXA1 protein expression was detected by flow cytometry as mean fluorescent intensity that shows the antibody reaction proteins. Our findings showed megakaryocytic differentiation of about 28% of umbilical cord blood CD133+ stem cells with bright expression of CD42/CD61 and CD41 in parallel with increase in HoxA1 mRNA and protein level. Colony forming of CD61+ cells in Megacult demonstrated the colonogenic capacity of differentiated progenitor cells. In conclusion, MiR-10a has a role in megakaryocyte differentiation of stem cells via HOXA1 transcription factor targeting.

引用

页码：93 / 100

页数：8

共 35 条

[1] The functions of animal microRNAs [J].

Ambros, V .

NATURE, 2004, 431 (7006) :350-355

[2] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].

Bartel, David P. .

CELL, 2007, 131 (04) :11-29

[3] RNA silencing in plants [J].

Baulcombe, D .

NATURE, 2004, 431 (7006) :356-363

[4] Aberrant expression of microRNA in polycythemia vera [J].

Bruchova, Hana ;

Merkerova, Michaela ;

Prchal, Josef T. .

HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 (07) :1009-1016

[5]

Bruno S, 2003, HAEMATOLOGICA, V88, P379

[6] MicroRNAs as regulators of mammalian hematopoiesis [J].

Chen, CZ ;

Lodish, HF .

SEMINARS IN IMMUNOLOGY, 2005, 17 (02) :155-165

[7] MicroRNAs modulate hematopoietic lineage differentiation [J].

Chen, CZ ;

Li, L ;

Lodish, HF ;

Bartel, DP .

SCIENCE, 2004, 303 (5654) :83-86

[8] MicroRNA expression profiling during human cord blood-derived CD34 cell erythropoiesis [J].

Choong, Meng Ling ;

Yang, Henry He ;

McNiece, Ian .

EXPERIMENTAL HEMATOLOGY, 2007, 35 (04) :551-564

[9] The role of HOX genes in malignant myeloid disease [J].

Eklund, Elizabeth A. .

CURRENT OPINION IN HEMATOLOGY, 2007, 14 (02) :85-89

[10] MicroRNAs 221 and 222 inhibit normal erythropoiesis and erythroleukemic cell growth via kit receptor down-modulation [J].

Felli, N ;

Fontana, L ;

Pelosi, E ;

Botta, R ;

Bonci, D ;

Facchiano, F ;

Liuzzi, F ;

Lulli, V ;

Morsilli, O ;

Santoro, S ;

Valtieri, M ;

Calin, GA ;

Liu, CG ;

Sorrentino, A ;

Croce, CM ;

Peschle, C .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (50) :18081-18086

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