Thioredoxin-Interacting Protein Regulates Hematopoietic Stem Cell Quiescence and Mobilization under Stress Conditions

被引:41
作者
Jeong, Mira [1 ,2 ]
Piao, Zheng-Hao [1 ]
Kim, Mi Sun [1 ]
Lee, Suk Hyung [1 ,2 ]
Yun, Sohyun [1 ]
Sun, Hu-nan [1 ]
Yoon, Suk Ran [1 ]
Chung, Jin Woong [1 ,3 ]
Kim, Tae-Don [1 ]
Jeon, Jun Ho [1 ]
Lee, Jiwon [1 ,2 ]
Kim, Hyun-Nam [4 ]
Choi, Je-Yong [4 ]
Choi, Inpyo [1 ,2 ]
机构
[1] Korea Res Inst Biosci & Biotechnol, Cell Therapy Res Ctr, Taejon 305333, South Korea
[2] Univ Sci & Technol, Dept Funct Genom, Taejon, South Korea
[3] Dong A Univ, Dept Biol Sci, Pusan, South Korea
[4] Kyungpook Natl Univ, Sch Med, Dept Biochem, Taegu, South Korea
关键词
SELF-RENEWAL; BONE-MARROW; GROWTH-FACTOR; BETA-CATENIN; NICHE; VDUP1; MAINTENANCE; ACTIVATION; PATHWAY; POOL;
D O I
10.4049/jimmunol.0804221
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hematopoietic stem cells (HSCs) are maintained in a quiescent state in bone marrow (BM) niches by intrinsic and extrinsic signals. The mechanisms regulating the quiescence and mobilization of HSCs, however, remain unclear. In this study, we report that the expression of thioredoxin-interacting protein (TXNIP) is decreased during HSC activation. In Txnip(-/-) mice, the long-term reconstituting HSC population is decreased and exhausted, and its capacity to repopulate is rapidly lost. These effects are associated with hyperactive Wnt signaling, an active cell cycle, and reduced p21 expression under conditions of stress. TXNIP deficiency reduced the CXCL12- and osteopontin-mediated interaction between HSCs and the bone marrow, and impaired homing and retention in the osteoblastic niche, resulting in mobilized HSCs. Therefore, we propose that TXNIP is essential for maintaining HSC quiescence and the interaction between HSCs and the BM niche. The Journal of Immunology, 2009, 183: 2495-2505.
引用
收藏
页码:2495 / 2505
页数:11
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