Skeletal development, bone remodeling, and hematopoiesis

被引:69
作者
Aguila, HL
Rowe, DW
机构
[1] Univ Connecticut, Ctr Hlth, Dept Immunol, Farmington, CT 06030 USA
[2] Univ Connecticut, Ctr Hlth, Dept Genet & Dev Biol, Farmington, CT 06030 USA
关键词
D O I
10.1111/j.0105-2896.2005.00333.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In adult mammals, the bone marrow microenvironment is defined by close interactions between cells derived from mesenchymal progenitors and cells derived from hematopoietic progenitors. The influence that one population of cells has over the other has been a matter of intense study since it was established that hematopoietic stem cells (HSCs) require support of stromal elements to engraft, self-renew, and progress towards lineage commitment. Within the stromal components, cells of the osteoblastic lineage have the ability to interact with HSCs, and it has been proposed that they could be one of the main cell types responsible for the generation and maintenance of hematopoietic niches. Possible molecular mechanisms involved in the interaction between osteoblastic and hematopoietic cells have been described. However, understanding the relative importance of each one of them, their production by defined cells, and their kinetics of appearance have been limited by the lack of in vivo models allowing the physical and/or temporal dissection of the components of the osteoblastic lineage. Here, we provide a summary of the evidence that have established the importance of osteoblasts in hematopoiesis, and we propose new experimental strategies that could help to define the nature of these interactions.
引用
收藏
页码:7 / 18
页数:12
相关论文
共 93 条
  • [1] Cotransplantation of human stromal cell progenitors into preimmune fetal sheep results in early appearance of human donor cells in circulation and boosts cell levels in bone marrow at later time points after transplantation
    Almeida-Porada, G
    Porada, CD
    Tran, N
    Zanjani, ED
    [J]. BLOOD, 2000, 95 (11) : 3620 - 3627
  • [2] Cotransplantation of human mesenchymal stem cells enhances human myelopoiesis and megakaryocytopoiesis in NOD/SCID mice
    Angelopoulou, M
    Novelli, E
    Grove, JE
    Rinder, HM
    Civin, C
    Cheng, LZ
    Krause, DS
    [J]. EXPERIMENTAL HEMATOLOGY, 2003, 31 (05) : 413 - 420
  • [3] ENGRAFTMENT OF A CLONAL BONE-MARROW STROMAL CELL-LINE INVIVO STIMULATES HEMATOPOIETIC RECOVERY FROM TOTAL-BODY IRRADIATION
    ANKLESARIA, P
    KASE, K
    GLOWACKI, J
    HOLLAND, CA
    SAKAKEENY, MA
    WRIGHT, JA
    FITZGERALD, TJ
    LEE, CY
    GREENBERGER, JS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) : 7681 - 7685
  • [4] Tie2/angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche
    Arai, F
    Hirao, A
    Ohmura, M
    Sato, H
    Matsuoka, S
    Takubo, K
    Ito, K
    Koh, GY
    Suda, T
    [J]. CELL, 2004, 118 (02) : 149 - 161
  • [5] ASHTON BA, 1980, CLIN ORTHOP RELAT R, P294
  • [6] BLAZSEK I, 1995, EXP HEMATOL, V23, P309
  • [7] Ontogenic emergence of the hematon, a morphogenetic stromal unit that supports multipotential hematopoietic progenitors in mouse bone marrow
    Blazsek, I
    Chagraoui, J
    Péault, B
    [J]. BLOOD, 2000, 96 (12) : 3763 - 3771
  • [8] Mesenchymal progenitor self-renewal deficiency leads to age-dependent osteoporosis in Sca-1/Ly-6A null mice
    Bonyadi, M
    Waldman, SD
    Liu, DM
    Aubin, JE
    Grynpas, MD
    Stanford, WL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (10) : 5840 - 5845
  • [9] Osteoblastic cells regulate the haematopoietic stem cell niche
    Calvi, LM
    Adams, GB
    Weibrecht, KW
    Weber, JM
    Olson, DP
    Knight, MC
    Martin, RP
    Schipani, E
    Divieti, P
    Bringhurst, FR
    Milner, LA
    Kronenberg, HM
    Scadden, DT
    [J]. NATURE, 2003, 425 (6960) : 841 - 846
  • [10] Carlevaro MF, 2000, J CELL SCI, V113, P59