Chondrogenic differentiation of amniotic fluid-derived stem cells

被引:0
作者
Yash M. Kolambkar
Alexandra Peister
Shay Soker
Anthony Atala
Robert E. Guldberg
机构
[1] Georgia Institute of Technology,Wallace H. Coulter Department of Biomedical Engineering
[2] Emory University,Parker H. Petit Institute for Bioengineering and Bioscience
[3] Georgia Institute of Technology,Wake Forest Institute for Regenerative Medicine
[4] Wake Forest University School of Medicine,George W. Woodruff School of Mechanical Engineering
[5] Georgia Institute of Technology,undefined
来源
Journal of Molecular Histology | 2007年 / 38卷
关键词
Cartilage repair; Chondrogenic differentiation; Amniotic fluid stem cells; Mesenchymal stem cells; Pellet culture; Transforming growth factor-beta;
D O I
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中图分类号
学科分类号
摘要
For regenerating damaged articular cartilage, it is necessary to identify an appropriate cell source that is easily accessible, can be expanded to large numbers, and has chondrogenic potential. Amniotic fluid-derived stem (AFS) cells have recently been isolated from human and rodent amniotic fluid and shown to be highly proliferative and broadly pluripotent. The purpose of this study was to investigate the chondrogenic potential of human AFS cells in pellet and alginate hydrogel cultures. Human AFS cells were expanded in various media conditions, and cultured for three weeks with growth factor supplementation. There was increased production of sulfated glycosaminoglycan (sGAG) and type II collagen in response to transforming growth factor-β (TGF-β) supplementation, with TGF-β1 producing greater increases than TGF-β3. Modification of expansion media supplements and addition of insulin-like growth factor-1 during pellet culture further increased sGAG/DNA over TGF-β1 supplementation alone. Compared to bone marrow-derived mesenchymal stem cells, the AFS cells produced less cartilaginous matrix after three weeks of TGF-β1 supplementation in pellet culture. Even so, this study demonstrates that AFS cells have the potential to differentiate along the chondrogenic lineage, thus establishing the feasibility of using these cells for cartilage repair applications.
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页码:405 / 413
页数:8
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