Molecular and cellular characterisation of highly purified stromal stem cells derived from human bone marrow

被引:767
作者
Gronthos, S [1 ]
Zannettino, ACW
Hay, SJ
Shi, ST
Graves, SE
Kortesidis, A
Simmons, PJ
机构
[1] Inst Med & Vet Sci, Div Haematol, Mesenchymal Stem Cell Grp, Adelaide, SA, Australia
[2] Matthew Roberts Fdn Lab, Inst Med & Vet Sci, Myeloma & Mesenchymal Res Grp, Adelaide, SA, Australia
[3] Univ Adelaide, Dept Orthopaed & Trauma, Adelaide, SA, Australia
[4] Natl Inst Dental & Craniofacial Res, Craniofacial & Skeletal Dis Branch, NIH, Bethesda, MD 20892 USA
[5] Royal Melbourne Hosp, Dept Orthopaed, Melbourne, Vic, Australia
[6] Peter MacCallum Canc Inst, Stem Cell Lab, Melbourne, Vic, Australia
关键词
bone marrow stroma; mesenchymal stem cells; STRO-1; bone; cartilage; adipose; CFU-F;
D O I
10.1242/jcs.00369
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Previous studies have provided evidence for the existence of adult human bone marrow stromal stem cells (BMSSCs) or mesenchymal stem cells. Using a combination of cell separation techniques, we have isolated an almost homogeneous population of BMSSCs from adult human bone marrow. Lacking phenotypic characteristics of leukocytes and mature stromal elements, BMSSCs are noncycling and constitutively express telomerase activity in vivo. This mesenchymal stem cell population demonstrates extensive proliferation and retains the capacity for differentiation into bone, cartilage and adipose tissue in vitro. In addition, clonal analysis demonstrated that individual BMSSC colonies exhibit a differential capacity to form new bone in vivo. These data are consistent with the existence of a second population of bone marrow stem cells in addition to those for the hematopoietic system. Our novel selection protocol provides a means to generate purified populations of BMSSCs for use in a range of different tissue engineering and gene therapy strategies.
引用
收藏
页码:1827 / 1835
页数:9
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