TY - JOUR
T1 - Reconstruction of an in vitro tissue-specific microenvironment to rejuvenate synovium-derived stem cells for cartilage tissue engineering
AU - He, Fan
AU - Chen, Xiaodong
AU - Pei, Ming
PY - 2009/12/1
Y1 - 2009/12/1
N2 - Joint injury results in cartilage lesions that are characterized by a poor repair response. Adult stem cells are immensely appealing for biological joint repair, such as cartilage tissue engineering and regeneration. However, adult stem cells gradually lose their stemness once they are removed from their in vivo niche for plating in plastic flasks. We utilized a tissue-specific stem cell, synovium-derived stem cell (SDSC), as a model to reconstruct an in vitro three-dimensional stem cell niche. After seeding on SDSC-derived extracellular matrix, the initially wide and flat SDSCs became thin and spindle shaped and were arranged in a three-dimensional configuration with typical stem cell phenotypes. A dramatic increase in cell number and a greatly enhanced chondrogenic capacity were observed, though surprisingly the extracellular matrix-treated SDSCs did not display concomitantly improved adipogenic or osteogenic potentials. Thus, we conclude that a tissue-specific stem cell can be used to prepare its own in vitro niche for stem cell proliferation while maintaining and enhancing its lineage-specific stemness. The ability to reconstitute the in vitro stem cell niche will greatly benefit SDSC-based therapy for cartilage defects.
AB - Joint injury results in cartilage lesions that are characterized by a poor repair response. Adult stem cells are immensely appealing for biological joint repair, such as cartilage tissue engineering and regeneration. However, adult stem cells gradually lose their stemness once they are removed from their in vivo niche for plating in plastic flasks. We utilized a tissue-specific stem cell, synovium-derived stem cell (SDSC), as a model to reconstruct an in vitro three-dimensional stem cell niche. After seeding on SDSC-derived extracellular matrix, the initially wide and flat SDSCs became thin and spindle shaped and were arranged in a three-dimensional configuration with typical stem cell phenotypes. A dramatic increase in cell number and a greatly enhanced chondrogenic capacity were observed, though surprisingly the extracellular matrix-treated SDSCs did not display concomitantly improved adipogenic or osteogenic potentials. Thus, we conclude that a tissue-specific stem cell can be used to prepare its own in vitro niche for stem cell proliferation while maintaining and enhancing its lineage-specific stemness. The ability to reconstitute the in vitro stem cell niche will greatly benefit SDSC-based therapy for cartilage defects.
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U2 - 10.1089/ten.tea.2009.0188
DO - 10.1089/ten.tea.2009.0188
M3 - Article
C2 - 19545204
AN - SCOPUS:72049125622
SN - 1937-3341
VL - 15
SP - 3809
EP - 3821
JO - Tissue Engineering - Part A
JF - Tissue Engineering - Part A
IS - 12
ER -