Downregulation of GATA-2 and overexpression of adipogenic gene-PPARγ in mesenchymal stem cells from patients with aplastic anemia

被引:59
作者
Xu, Yinyan
Takahashi, Yoshiyuki
Wang, Yue [2 ]
Hama, Asahito
Nishio, Nobuhiro
Muramatsu, Hideki
Tanaka, Makito
Yoshida, Nao
Villalobos, Itzel Bustos
Yagasaki, Hiroshi
Kojima, Seiji [1 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Pediat, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Jilin Univ, Dept Pediat, Hosp 1, Changchun 130023, Jilin, Peoples R China
关键词
TRANSCRIPTION FACTOR GATA-2; MARROW STROMAL CELLS; EXPRESSION;
D O I
10.1016/j.exphem.2009.09.005
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Aplastic anemia (AA) is characterized by a reduced number of hematopoietic stem cells and fatty replacement in the bone marrow. Transcriptional factor GATA-2 plays several important roles in both hematopoiesis and adipogenesis. Decreased levels of GATA-2 compromise the proliferation and survival of hematopoietic stem cells. GATA-2 suppresses adipocyte differentiation through direct inhibition of adipogenic factors, including peroxisome proliferator-activated receptor-gamma (PPAR gamma). Previous studies have shown that expression of GATA-2 is decreased in marrow CD34-positive cells in AA. To elucidate the mechanisms of fatty marrow replacement, we evaluated the mRNA expression for GATA-2 and PPAR gamma in mesenchymal stem cells (MSCs) from patients with AA by quantitative real-time polymerase chain reaction. GATA-2 expression by MSCs from AA patients was significantly lower than in normal subjects. Conversely, expression of PPAR gamma was significantly higher in AA patients. Western blot analysis demonstrated that protein levels of GATA-2 were lower in AA patients than those in normal subjects. Moreover, incubation with interferon-gamma induced downregulation of GATA-2 levels in MSCs from normal subjects. These findings indicate that fatty marrow replacement in AA patients can be explained by downregulation of GATA-2 and overexpression of PPAR gamma in MSCs. Decreased expression of GATA-2 might be responsible for the pathogenesis and development of the clinical features of the disease. (C) 2009 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc.
引用
收藏
页码:1393 / 1399
页数:7
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