Mesenchymal progenitor cells localize within hematopoietic sites throughout ontogeny

被引:120
作者
Mendes, SC [1 ]
Robin, C [1 ]
Dzierzak, E [1 ]
机构
[1] Erasmus Univ, Ctr Med, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
来源
DEVELOPMENT | 2005年 / 132卷 / 05期
关键词
mesenchyme; hematopoiesis; AGM; development; embryo;
D O I
10.1242/dev.01615
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mesenchymal stem cells (MSCs) have great clinical potential for the replacement and regeneration of diseased or damaged tissue. They are especially important in the production of the hematopoietic microenvironment, which regulates the maintenance and differentiation of hematopoietic stem cells (HSCs). In the adult, MSCs and their differentiating progeny are found predominantly in the bone marrow (BM). However, it is as yet unknown in which embryonic tissues MSCs reside and whether there is a localized association of these cells within hematopoietic sites during development. To investigate the embryonic origins of these cells, we performed anatomical mapping and frequency analysis of mesenchymal progenitors at several stages of mouse ontogeny. We report here the presence of mesenchymal progenitors, with the potential to differentiate into cells of the osteogenic, adipogenic and chondrogenic lineages, in most of the sites harboring hematopoietic cells. They first appear in the aorta-gonadmesonephros (AGM) region at the time of HSC emergence. However, at this developmental stage, their presence is independent of HSC activity. They increase numerically during development to a plateau level found in adult BM. Additionally, mesenchymal progenitors are found in the embryonic circulation. Taken together, these data show a co-localization of mesenchymal progenitor/stem cells to the major hematopoietic territories, suggesting that, as development proceeds, mesenchymal progenitors expand within these potent hematopoietic sites.
引用
收藏
页码:1127 / 1136
页数:10
相关论文
共 51 条
[31]   Definitive hematopoiesis is autonomously initiated by the AGM region [J].
Medvinsky, A ;
Dzierzak, E .
CELL, 1996, 86 (06) :897-906
[32]  
Minasi MG, 2002, DEVELOPMENT, V129, P2773
[33]   In vitro maintenance of highly purified, transplantable hematopoietic stem cells [J].
Moore, KA ;
Ema, H ;
Lemischka, IR .
BLOOD, 1997, 89 (12) :4337-4347
[34]   THE PURIFICATION AND CHARACTERIZATION OF FETAL LIVER HEMATOPOIETIC STEM-CELLS [J].
MORRISON, SJ ;
HEMMATI, HD ;
WANDYCZ, AM ;
WEISSMAN, IL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (22) :10302-10306
[35]   DEVELOPMENT OF HEMATOPOIETIC STEM-CELL ACTIVITY IN THE MOUSE EMBRYO [J].
MULLER, AM ;
MEDVINSKY, A ;
STROUBOULIS, J ;
GROSVELD, F ;
DZIERZAK, E .
IMMUNITY, 1994, 1 (04) :291-301
[36]  
North T, 1999, DEVELOPMENT, V126, P2563
[37]  
Oostendorp RAJ, 2002, J CELL SCI, V115, P2099
[38]   Stromal cell lines from mouse aorta-gonads-mesonephros subregions are potent supporters of hematopoietic stem cell activity [J].
Oostendorp, RAJ ;
Harvey, KN ;
Kusadasi, N ;
de Bruijn, MFTR ;
Saris, C ;
Ploemacher, RE ;
Medvinsky, AL ;
Dzierzak, EA .
BLOOD, 2002, 99 (04) :1183-1189
[39]  
OWEN ME, 1987, J CELL SCI, V87, P731
[40]   Isolation and characterization of human clonogenic osteoblast progenitors immunoselected from fetal bone marrow stroma using STRO-1 monoclonal antibody [J].
Oyajobi, BO ;
Lomri, A ;
Hott, M ;
Marie, PJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (03) :351-361