Gene and miRNA Expression Profiles of Hematopoietic Progenitor Cells Vary Depending on Their Origin

被引:13
作者
Baez, Alicia [1 ]
Martin-Antonio, Beatriz [2 ,3 ]
Piruat, Jose I. [1 ]
Victoria Barbado, Maria [1 ]
Prats, Concepcion [1 ]
Alvarez-Laderas, Isabel [1 ]
Carmona, Magdalena [1 ]
Antonio Perez-Simon, Jose [1 ]
Urbano-Ispizua, Alvaro [2 ,3 ]
机构
[1] IBIS CSIC Univ Seville, Inst Biomed Sevilla, Dept Hematol, Hosp Univ Virgen del Rocio, Seville, Spain
[2] Univ Barcelona, Dept Hematol, Hosp Clin IDIBAPS, E-08007 Barcelona, Spain
[3] Univ Barcelona, Inst Res Josep Carreras, E-08007 Barcelona, Spain
关键词
Hematopoietic progenitor cell; miRNA; Gene expression; VERSUS-HOST-DISEASE; PERIPHERAL-BLOOD; BONE-MARROW; CORD BLOOD; STEM-CELLS; DIFFERENTIATION; MICRORNAS; PROLIFERATION; RECEPTOR; PLAY;
D O I
10.1016/j.bbmt.2014.01.022
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hematopoietic progenitor cells (HPCs) from granulocyte colony-stimulating factor (G-CSF) mobilized peripheral blood (G-PB), bone marrow (BM), or umbilical cord blood (CB) have differing biological properties and differing kinetics of engraftment post-transplantation, which might be explained, at least in part, by differing gene and miRNA expression patterns. To assess the differences in gene and miRNA expression, we analyzed whole genome expression profiles as well as the expression of 384 miRNAs in CD34(+) cells isolated from 18 healthy individuals (6 individuals per subtype of HPC source). We identified 43 genes and 36 miRNAs differentially expressed in the various CD34(+) cell sources. We observed that CD34(+) cells from CB and BM showed similar gene and miRNA expression profiles, whereas CD34(+) cells from G-PB had a very different expression pattern. Remarkably, 20 of the differentially expressed genes are targets of the differentially expressed miRNAs. Of note, the majority of genes differentially expressed in CD34(+) cells from G-PB are involved in cell cycle regulation, promoting the process of proliferation, survival, hematopoiesis, and cell signaling, and are targets of overexpressed and underexpressed miRNAs in CD34(+) cells from the same source. These data suggest significant differences in gene and miRNA expression among the various HPC sources used in transplantation. We hypothesize that the differentially expressed genes and miRNAs involved in cell cycle and proliferation might explain the differing kinetics of engraftment observed after transplantation of hematopoietic stem cells obtained from these different sources. (c) 2014 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:630 / 639
页数:10
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