Human embryonic stem cells:: lessons from stem cell niches in vivo

被引:16
作者
Bendall, Sean C. [1 ,2 ,3 ]
Stewart, Morag H. [1 ,2 ]
Bhatia, Mickie [1 ,2 ]
机构
[1] McMaster Univ, McMaster Stem Cell & Canc Res Inst, Michael G DeGroote Sch Med, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Dept Biochem, Hamilton, ON L8N 3Z5, Canada
[3] Univ Western Ontario, Dept Biochem, Dan Rix Prot Identificat Eacil, Schulich Sch Med & Dent, London, ON N6A 5C1, Canada
关键词
cell-based therapy; differentiation; embroid body; hdF; hESC; human embryonic stem cells; microenvironment; niche; pluripotency; regenerative medicine; self-renewal;
D O I
10.2217/17460751.3.3.365
中图分类号
Q813 [细胞工程];
学科分类号
摘要
In vivo the stem cell niche is an essential component in controlling and maintaining the stem cells' ability to survive and respond to injury. Human embryonic stem cells (hESCS) appear to be an exception to this rule as they can be removed from their blastocytic microenvironment and maintained indefinitely in vitro. However, recent observations reveal the existence of an autonomously derived in vitro hESC niche. This provides a previously unappreciated mechanism to control hESC expansion and differentiation. Recognizing this, it may now be possible to take aspects of in vivo stem cell niches, namely extracellular matrices, paracrine signals and accessory cell types, and exploit them in order to gain fidelity in directed hESC differentiation. In doing so, routine customization of hESC lines and their application in regenerative therapies may be further enhanced using unique hESC niche-based approaches.
引用
收藏
页码:365 / 376
页数:12
相关论文
共 83 条
[1]   Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture [J].
Amit, M ;
Carpenter, MK ;
Inokuma, MS ;
Chiu, CP ;
Harris, CP ;
Waknitz, MA ;
Itskovitz-Eldor, J ;
Thomson, JA .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :271-278
[2]   Nanoliter-scale synthesis of arrayed biomaterials and application to human embryonic stem cells [J].
Anderson, DG ;
Levenberg, S ;
Langer, R .
NATURE BIOTECHNOLOGY, 2004, 22 (07) :863-866
[3]   From teratocarcinomas to embryonic stem cells [J].
Andrews, PW .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2002, 357 (1420) :405-417
[4]   Identification of stem cells in small intestine and colon by marker gene Lgr5 [J].
Barker, Nick ;
van Es, Johan H. ;
Kuipers, Jeroen ;
Kujala, Pekka ;
van den Born, Maaike ;
Cozijnsen, Miranda ;
Haegebarth, Andrea ;
Korving, Jeroen ;
Begthel, Harry ;
Peters, Peter J. ;
Clevers, Hans .
NATURE, 2007, 449 (7165) :1003-U1
[5]   Activin A maintains pluripotency of human embryonic stem cells in the absence of feeder layers [J].
Beattie, GM ;
Lopez, AD ;
Bucay, N ;
Hinton, A ;
Firpo, MT ;
King, CC ;
Hayek, A .
STEM CELLS, 2005, 23 (04) :489-495
[6]   CYTOLOGICAL DEMONSTRATION OF CLONAL NATURE OF SPLEEN COLONIES DERIVED FROM TRANSPLANTED MOUSE MARROW CELLS [J].
BECKER, AJ ;
TILL, JE ;
MCCULLOCH, EA .
NATURE, 1963, 197 (486) :452-&
[7]   IGF and FGF cooperatively establish the regulatory stem cell niche of pluripotent human cells in vitro [J].
Bendall, Sean C. ;
Stewart, Morag H. ;
Menendez, Pablo ;
George, Dustin ;
Vijayaragavan, Kausalia ;
Werbowetski-Ogilvie, Tamra ;
Ramos-Mejia, Veronica ;
Rouleau, Anne ;
Yang, Jiabi ;
Bosse, Marc ;
Lajoie, Gilles ;
Bhatia, Mickie .
NATURE, 2007, 448 (7157) :1015-U3
[8]   Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice [J].
Bhatia, M ;
Wang, JCY ;
Kapp, U ;
Bonnet, D ;
Dick, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5320-5325
[9]   Hematopoiesis from human embryonic stem cells [J].
Bhatia, Mickie .
HEMATOPOIETIC STEM CELLS VI, 2007, 1106 :219-222
[10]   Bone marrow stromal stem cells: Nature, biology, and potential applications [J].
Bianco, P ;
Riminucci, M ;
Gronthos, S ;
Robey, PG .
STEM CELLS, 2001, 19 (03) :180-192