Targeted delivery of progenitor cells for cartilage repair

被引:55
|
作者
Dennis, JE
Cohen, N
Goldberg, VM
Caplan, AI
机构
[1] Case Western Reserve Univ, Dept Biol, Skeletal Res Ctr, Cleveland, OH 44106 USA
[2] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[3] Dept Orthopaed, IL-63455 Tel Aviv, Israel
[4] Case Western Reserve Univ, Dept Orthopaed, Skeletal Res Ctr, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
cartilage; progenitor cells; targeting; repair;
D O I
10.1016/j.orthres.2003.12.002
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
An approach for promoting the adherence of chondrogenic progenitor cells to specific matrix molecules has been tested in a cartilage defect model. Culture-expanded pre-chondrocytes fluorescently labeled with a vital dye were coated by a two-step method wherein lipidated protein G was first allowed to intercalate into cell membranes, and a second incubation in a solution of antibodies to cartilage matrix antigens allowed the binding of the antibodies to the protein G, on the external surface of the cell. The coating technique (termed "cell painting") does not effect cell viability or inhibit growth and chondrogenic potential. Painted cells were then added to rabbit cartilage explants that had a partial-thickness defect, washed, and prepared for histological examination and for confocal microscopy. The histological observations and the confocal observations and fluorescent intensity quantification consistently demonstrated that progenitor cells painted with multiple antibodies were capable of preferential binding to the exposed cartilage matrix within the defect. These results demonstrate that painting cell membranes with antibodies to matrix molecules is an effective method for promoting the adherence of stem or progenitor cells to a cartilage injury site. (C) 2003 Orthopaedic Research Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:735 / 741
页数:7
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