On signaling pathways: hematopoietic stem cell specification from hemogenic endothelium

被引:7
作者
Long Yan [1 ]
Huang He [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Bone Marrow Transplantat Ctr, Hangzhou 310003, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
HSCs; hemogenic endothelium; signaling pathways; FATE; WNT;
D O I
10.1007/s11427-015-4976-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hematopoietic stem cells (HSCs) are specified and generated during the embryonic development and have remarkable potential to replenish the full set of blood cell lineages. Researchers have long been interested in clarifying the molecular events involved in HSC specification. Many studies have reported the development of methods for generating functional hematopoietic cells from pluripotent stem cells (PSCs-embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs)) for decades. However, the generation of HSCs with robust long-term repopulation potential remains a swingeing challenge, of which a major factor contributing to this failure is the difficulty to define the intraembryonic signals related to the specification of HSCs. Since HSCs directly derive from hemogenic endothelium, in this review, we summarize both in vivo and in vitro studies on conserved signaling pathways that control the specification of HSCs from hemogenic endothelial cells.
引用
收藏
页码:1256 / 1261
页数:6
相关论文
共 65 条
  • [1] Biomechanical forces promote embryonic haematopoiesis
    Adamo, Luigi
    Naveiras, Olaia
    Wenzel, Pamela L.
    McKinney-Freeman, Shannon
    Mack, Peter J.
    Gracia-Sancho, Jorge
    Suchy-Dicey, Astrid
    Yoshimoto, Momoko
    Lensch, M. William
    Yoder, Mervin C.
    Garcia-Cardena, Guillermo
    Daley, George Q.
    [J]. NATURE, 2009, 459 (7250) : 1131 - U120
  • [2] Notch signaling: Cell fate control and signal integration in development
    Artavanis-Tsakonas, S
    Rand, MD
    Lake, RJ
    [J]. SCIENCE, 1999, 284 (5415) : 770 - 776
  • [3] Notch signaling distinguishes 2 waves of definitive hematopoiesis in the zebrafish embryo
    Bertrand, Julien Y.
    Cisson, Jennifer L.
    Stachura, David L.
    Traver, David
    [J]. BLOOD, 2010, 115 (14) : 2777 - 2783
  • [4] Haematopoietic stem cells derive directly from aortic endothelium during development
    Bertrand, Julien Y.
    Chi, Neil C.
    Santoso, Buyung
    Teng, Shutian
    Stainier, Didier Y. R.
    Traver, David
    [J]. NATURE, 2010, 464 (7285) : 108 - U120
  • [5] An in vivo reporter of BMP signaling in organogenesis reveals targets in the developing kidney
    Blank, Ulrika
    Seto, Marianne L.
    Adams, Derek C.
    Wojchowski, Don M.
    Karolak, Michele J.
    Oxburgh, Leif
    [J]. BMC DEVELOPMENTAL BIOLOGY, 2008, 8
  • [6] In vivo imaging of haematopoietic cells emerging from the mouse aortic endothelium
    Boisset, Jean-Charles
    van Cappellen, Wiggert
    Andrieu-Soler, Charlotte
    Galjart, Niels
    Dzierzak, Elaine
    Robin, Catherine
    [J]. NATURE, 2010, 464 (7285) : 116 - U131
  • [7] Hematopoietic stem cell fate is established by the Notch-Runx pathway
    Burns, CE
    Traver, D
    Mayhall, E
    Shepard, JL
    Zon, LI
    [J]. GENES & DEVELOPMENT, 2005, 19 (19) : 2331 - 2342
  • [8] Erythroid/Myeloid Progenitors and Hematopoietic Stem Cells Originate from Distinct Populations of Endothelial Cells
    Chen, Michael J.
    Li, Yan
    De Obaldia, Maria Elena
    Yang, Qi
    Yzaguirre, Amanda D.
    Yamada-Inagawa, Tomoko
    Vink, Chris S.
    Bhandoola, Avinash
    Dzierzak, Elaine
    Speck, Nancy A.
    [J]. CELL STEM CELL, 2011, 9 (06) : 541 - 552
  • [9] Choi K, 1998, DEVELOPMENT, V125, P725
  • [10] Signalling pathways that control vertebrate haematopoietic stem cell specification
    Clements, Wilson K.
    Traver, David
    [J]. NATURE REVIEWS IMMUNOLOGY, 2013, 13 (05) : 336 - 348