Hematopoietic cells from bone marrow have the potential to differentiate into cardiomyocytes in vitro

被引:38
作者
Eisenberg, LM [1 ]
Burns, L [1 ]
Eisenberg, CA [1 ]
机构
[1] Med Univ S Carolina, Dept Cell Biol & Anat, Charleston, SC 29425 USA
来源
ANATOMICAL RECORD PART A-DISCOVERIES IN MOLECULAR CELLULAR AND EVOLUTIONARY BIOLOGY | 2003年 / 274A卷 / 01期
关键词
cardiac; stem cells; differentiation; blood; macrophages;
D O I
10.1002/ar.a.10106
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Recent studies have indicated that hematopoietic progenitor cells (HPCs) have the capacity to form cardiomyocytes. In the present study, we further examined the cardiac competence of HPCs by asking whether these cells by themselves can be provoked to undergo cardiac differentiation. Our data indicate that in response to growth factor treatment, HPCs from avian bone marrow (BM) can undergo cardiac differentiation, as indicated by their expression of multiple cardiac transcription factors and sarcomeric proteins. Furthermore, coculture experiments with adult mouse BM cells and embryonic heart tissue confirmed that HPCs are able to both integrate into cardiac tissue and differentiate into cardiomyocytes. In an additional set of experiments, we investigated whether other hematopoietic populations might possess cardiac potential by examining whether blood cells that normally are recruited to damaged tissue might act as a source of newly generated cardiomyocytes. Remarkably, macrophages cocultured with cardiac explants also demonstrated an ability to integrate into contractile heart tissue and undergo cardiac differentiation. Thus, our data suggest that the capacity of blood cells to transdifferentiate into cardiomyocytes is not limited to classically defined hematopoietic progenitors. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:870 / 882
页数:13
相关论文
共 52 条
[31]   Combined BMP-2 and FGP-4, but neither factor alone, induces cardiogenesis in non-precardiac embryonic mesoderm [J].
Lough, J ;
Barron, M ;
Brogley, M ;
Sugi, Y ;
Bolender, DL ;
Zhu, XL .
DEVELOPMENTAL BIOLOGY, 1996, 178 (01) :198-202
[32]   Treatment of traumatic brain injury in female rats with intravenous administration of bone marrow stromal cells [J].
Mahmood, A ;
Lu, D ;
Wang, L ;
Li, Y ;
Lu, M ;
Chopp, M .
NEUROSURGERY, 2001, 49 (05) :1196-1203
[33]   Regeneration of the urodele limb: A review [J].
Nye, HLD ;
Cameron, JA ;
Chernoff, EAG ;
Stocum, DL .
DEVELOPMENTAL DYNAMICS, 2003, 226 (02) :280-294
[34]   Mobilized bone marrow cells repair the infarcted heart, improving function and survival [J].
Orlic, D ;
Kajstura, J ;
Chimenti, S ;
Limana, F ;
Jakoniuk, I ;
Quaini, F ;
Nadal-Ginard, B ;
Bodine, DM ;
Leri, A ;
Anversa, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) :10344-10349
[35]   Bone marrow cells regenerate infarcted myocardium [J].
Orlic, D ;
Kajstura, J ;
Chimenti, S ;
Jakoniuk, I ;
Anderson, SM ;
Li, BS ;
Pickel, J ;
McKay, R ;
Nadal-Ginard, B ;
Bodine, DM ;
Leri, A ;
Anversa, P .
NATURE, 2001, 410 (6829) :701-705
[36]   Chimerism of the transplanted heart (Publication with Expression of Concern. See vol. 379, pg. 1870, 2018) [J].
Quaini, F ;
Urbanek, K ;
Beltrami, AP ;
Finato, N ;
Beltrami, CA ;
Nadal-Ginard, B ;
Kajstura, J ;
Leri, A ;
Anversa, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (01) :5-15
[37]   Flt-1, vascular endothelial growth factor receptor 1, is a novel cell surface marker for the lineage of monocyte-macrophages in humans [J].
Sawano, A ;
Iwai, S ;
Sakurai, Y ;
Ito, M ;
Shitara, K ;
Nakahata, T ;
Shibuya, M .
BLOOD, 2001, 97 (03) :785-791
[38]   BMP2 is required for early heart development during a distinct time period [J].
Schlange, T ;
Andrée, B ;
Arnold, HH ;
Brand, T .
MECHANISMS OF DEVELOPMENT, 2000, 91 (1-2) :259-270
[39]  
Schultheiss TM, 1995, DEVELOPMENT, V121, P4203
[40]   HAND proteins: Molecular mediators of cardiac development and congenital heart disease [J].
Srivastava, D .
TRENDS IN CARDIOVASCULAR MEDICINE, 1999, 9 (1-2) :11-18