Hematopoietic vascular and cardiac fates of bone marrow-derived stem cells

被引:84
作者
Hirschi, KK
Goodell, MA
机构
[1] Baylor Coll Med, Ctr Cell & Gene Therapy, Childrens Nutr Res Ctr, Dept Pediat, Houston, TX 77030 USA
[2] Baylor Coll Med, Ctr Cell & Gene Therapy, Childrens Nutr Res Ctr, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Pediat Immunol & Human & Mol Genet, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
关键词
bone marrow; hematopoietic stem cells; vascular progenitors; muscle progenitors; stem cell plasticity;
D O I
10.1038/sj.gt.3301722
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bone marrow contains many cell types, including stroma, vascular cells, adipocytes, osteoblasts and osteoclasts, as well as mesenchymal stem cells and hematopoietic stem cells. It was previously thought that cells within bone marrow solely functioned to regenerate cells within the marrow, as well as all circulating hematopoietic cells in peripheral blood. Recent reports, however, suggest that marrow-derived cells can also regenerate other cell types, including cardiac muscle, liver cell types, neuronal and non-neuronal cell types of the brain, as well as endothelial cells and osteoblasts. These multiple cell types could have originated from either of the stem cell populations within bone marrow or potentially other precursors. Therefore, it is not entirely clear whether each of these distinct cell lineages has a true progenitor within marrow or whether the marrow contains a multipotent population of cells that has been set aside during embryogenesis for postnatal repair and remodeling of a variety of tissues. It is clear, however, that directing the fate of bone marrow-derived progenitors (ie toward hematopoietic, vascular or cardiac cell fates) can only be accomplished if the phenotype of the stem cells is defined, and their homing and differentiation programs are elucidated. Much work is focused on these issues, wherein lie the key to harnessing the potential of adult stem cells for autologous cell and gene therapy.
引用
收藏
页码:648 / 652
页数:5
相关论文
共 51 条
  • [21] Human embryonic stem cells can differentiate into myocytes with structural and functional properties of cardiomyocytes
    Kehat, I
    Kenyagin-Karsenti, D
    Snir, M
    Segev, H
    Amit, M
    Gepstein, A
    Livne, E
    Binah, O
    Itskovitz-Eldor, J
    Gepstein, L
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (03) : 407 - 414
  • [22] Keller G, 2001, COLD SPRING HARBOR M, P329
  • [23] Genetically selected cardiomyocytes from differentiating embryonic stem cells form stable intracardiac grafts
    Klug, MG
    Soonpaa, MH
    Koh, GY
    Field, LJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (01) : 216 - 224
  • [24] Neovascularization of ischemic myocardium by human bone-marrow-derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function
    Kocher, AA
    Schuster, MD
    Szabolcs, MJ
    Takuma, S
    Burkhoff, D
    Wang, J
    Homma, S
    Edwards, NM
    Itescu, S
    [J]. NATURE MEDICINE, 2001, 7 (04) : 430 - 436
  • [25] STABLE FETAL CARDIOMYOCYTE GRAFTS IN THE HEARTS OF DYSTROPHIC MICE AND DOGS
    KOH, GY
    SOONPAA, MH
    KLUG, MG
    PRIDE, HP
    COOPER, BJ
    ZIPES, DP
    FIELD, LJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (04) : 2034 - 2042
  • [26] DEVELOPMENTAL POTENTIAL AND DYNAMIC BEHAVIOR OF HEMATOPOIETIC STEM-CELLS
    LEMISCHKA, IR
    RAULET, DH
    MULLIGAN, RC
    [J]. CELL, 1986, 45 (06) : 917 - 927
  • [27] Origins of circulating endothelial cells and endothelial outgrowth from blood
    Lin, Y
    Weisdorf, D
    Solovey, A
    Hebbel, RP
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (01) : 71 - 77
  • [28] Endothelial-perivascular cell signaling in vascular development:: lessons from knockout mice
    Lindahl, P
    Hellström, M
    Kalén, M
    Betsholtz, C
    [J]. CURRENT OPINION IN LIPIDOLOGY, 1998, 9 (05) : 407 - 411
  • [29] MCCLANAHAN T, 1993, BLOOD, V81, P2903
  • [30] Turning blood into brain:: Cells bearing neuronal antigens generated in vivo from bone marrow
    Mezey, É
    Chandross, KJ
    Harta, G
    Maki, RA
    McKercher, SR
    [J]. SCIENCE, 2000, 290 (5497) : 1779 - 1782