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Blood:调控造血干细胞的信号通路
发布时间:2007-11-3 15:22:04 来源:生命科学动态 共点击0
10月的《血液》(Blood)杂志报道了,瑞典隆德(Lund)大学医院干细胞研究中心人员最新总结的调控造血干细胞的多条信号通路。  

    造血干细胞(HSCs)是能自我更新、有较强分化发育和再生能力、可以产生各种类型血细胞的始祖细胞。HSCs是目前研究最为透彻的人类干细胞。多年来,造血干细胞一直作为干细胞生物学研究的基本模型。虽然,已能明确HSCs的功能,并且可以进行纯化,但调控HSCs自我更新和分化的分子机制和信号通路仍然是个谜。  

    近来,Notch、Wnt、Sonic  hedgehog  (Shh)  和Smad信号通路的研究推进了对HSCs调控的了解。HSCs存在于复杂的骨髓环境中,有着自我更新和分化信号最佳的微环境。这些信号通路使我们能更好地了解HSCs调控、骨髓微环境及外在因素作用于HSCs内部等。  

    由此,研究者高度关注最新调控造血干细胞信号通路的进展。(医学空间)

原始出处:

Blood First Edition Paper, prepublished online October 3, 2007; DOI 10.1182/blood-2007-07-075168.

Submitted July 22, 2007
Accepted September 30, 2007

Signaling pathways governing stem cell fate

Ulrika Blank, Goran Karlsson, and Stefan Karlsson*

Molecular Med. & Gene Therapy, Inst. of Laboratory Med., & The Lund Strategic Research Center for Stem Cell Biology & Cell Therapy, Lund University Hospital, Lund, Sweden

* Corresponding author; email: stefan.karlsson@med.lu.se .

Hematopoietic stem cells (HSCs) are historically the most thoroughly characterized type of adult stem cell, and the hematopoietic system has served as a principal model structure of stem cell biology for several decades. However, paradoxically, while HSCs can be defined by function and even purified to near-homogeneity, the intricate molecular machinery and the signaling mechanisms regulating fate events such as self-renewal and differentiation have remained elusive. Recently, several developmentally conserved signaling pathways have emerged as important control devices of HSC fate, including Notch, Wnt, Sonic hedgehog (Shh) and Smad pathways. HSCs reside in a complex environment in the bone marrow (BM), providing a niche that optimally balances signals that control self-renewal and differentiation. These signaling circuits provide a valuable structure for our understanding of how HSC regulation occurs, concomitantly with providing information of how the BM microenvironment couples and integrates extrinsic with intrinsic HSC fate determinants. It is the focus of this review to highlight some of the most recent developments concerning signaling pathways governing HSC fate.

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