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

被引:0
作者
K K Hirschi
M A Goodell
机构
[1] Children's Nutrition Research Center,Departments of Pediatrics and Molecular and Cellular Biology
[2] Baylor College of Medicine,Department of Pediatrics
[3] Center for Cell and Gene Therapy,undefined
[4] Immunology and Human and Molecular Genetics,undefined
[5] Baylor College of Medicine,undefined
[6] Center for Cell and Gene Therapy,undefined
来源
Gene Therapy | 2002年 / 9卷
关键词
bone marrow; hematopoietic stem cells; vascular progenitors; muscle progenitors; stem cell plasticity;
D O I
暂无
中图分类号
学科分类号
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:4
相关论文
共 87 条
[1]  
Ferrari G(1998)Muscle regeneration by bone marrow-derived myogenic progenitors Science 279 1528-1530
[2]  
Bittner RE(1999)Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice Anat Embryol (Berl) 199 391-396
[3]  
Shi Q(1998)Evidence for circulating bone marrow-derived endothelial cells Blood 92 362-367
[4]  
Horwitz EM(1999)Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta Nat Med 5 309-313
[5]  
Petersen BE(1999)Bone marrow as a potential source of hepatic oval cells Science 284 1168-1170
[6]  
Theise ND(2000)Derivation of hepatocytes from bone marrow cells in mice after radiation-induced myeloablation Hepatology 31 235-240
[7]  
Theise ND(2000)Liver from bone marrow in humans Hepatology 32 11-16
[8]  
Brazelton TR(2000)From marrow to brain: expression of neuronal phenotypes in adult mice Science 290 1775-1779
[9]  
Rossi FM(2000)Turning blood into brain: cells bearing neuronal antigens generated in vivo from bone marrow Science 290 1779-1782
[10]  
Keshet GI(1997)Hematopoietic cells differentiate into both microglia and macroglia in the brains of adult mice Proc Natl Acad Sci USA 94 4080-4085