The CD34-like protein PODXL and α6-integrin (CD49f) identify early progenitor MSCs with increased clonogenicity and migration to infarcted heart in mice

被引:149
作者
Lee, Ryang Hwa [1 ]
Seo, Min Jeong [1 ]
Pulin, Andrey A. [1 ]
Gregory, Carl A. [1 ]
Ylostalo, Joni [1 ]
Prockop, Darwin J. [1 ]
机构
[1] Tulane Univ, Hlth Sci Ctr, Ctr Gene Therapy, New Orleans, LA 70118 USA
基金
美国国家卫生研究院;
关键词
MESENCHYMAL STEM-CELLS; MARROW STROMAL CELLS; HUMAN-BONE-MARROW; HEMATOPOIETIC STEM; GROWTH-FACTOR; MONOCLONAL-ANTIBODIES; CLINICAL-TRIALS; CANCER-CELLS; IN-VITRO; IDENTIFICATION;
D O I
10.1182/blood-2007-12-128702
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We screened for surface proteins expressed only by the early progenitor cells present in low-passage, low-density cultures of the adult stem/progenitor cells from bone marrow referred to as mesenchymal stem cells or multipotent stromal cells (MSCs). Six proteins were identified that were selectively expressed in the early progenitors: podocalyxin-like protein (PODXL), alpha 6-integrin (CD49f), alpha 4-integrin (CD49d), c-Met, CXCR4, and CX3CR1. All were previously shown to be involved in cell trafficking or tumor progression. Antibodies to CD49f and PODXL, a sialomucin in the CD34 family, were the most robust for FACScan assays. PODXLhi/CD49f(hi) MSCs were more clonogenic and differentiated more effi-than PODXLlo/CD49f(lo) cells. Inhibition of expression of PODXL with RNA interference caused aggregation of the cells. Furthermore, PODXLhi/CD49f(hi) MSCs were less prone to produce lethal pulmonary emboli, and larger numbers were recovered in heart and kidney after intravenous infusion into mice with myocardial infarcts. (Blood. 2009;113:816-826)
引用
收藏
页码:816 / 826
页数:11
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