alexa Three-Dimensional Cell Expansion Substrate for Cartilage Tissue Engineering and Regeneration: A Comparison in Decellularized Matrix Deposited by Synovium-Derived Stem Cells and Chondrocytes
ISSN: 2157-7552

Journal of Tissue Science & Engineering
Open Access

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Research Article

Three-Dimensional Cell Expansion Substrate for Cartilage Tissue Engineering and Regeneration: A Comparison in Decellularized Matrix Deposited by Synovium-Derived Stem Cells and Chondrocytes

M. Pei1,2,3*, F. He1,2 and L. Wei4

1Stem Cell and Tissue Engineering Laboratory, Department of Orthopaedics, West Virginia University, Morgantown, WV 26506

2Division of Exercise Physiology, West Virginia University, Morgantown, WV 26506

3Mechnical and Aerospace Engineering, West Virginia University, Morgantown, WV 26506

4Department of Orthopaedics, Brown Medical School/Rhode Island Hospital, Providence, RI 02903

Corresponding Author:
Dr. Ming Pei, M.D., Ph.D.,
Stem Cell and Tissue Engineering Laboratory
PO Box 9196, Department of Orthopaedics
West Virginia University, One Medical Center Drive
Morgantown, WV 26506-9196, USA
Tel: 304-293- 1072
Fax: 304-293-7070
Email: [email protected]

Received date: June 29, 2011; Accepted date: July 14, 2011; Published date: July 16, 2011

Citation: Pei M, He F, Wei L (2010) Three-Dimensional Cell Expansion Substrate For Cartilage Tissue Engineering And Regeneration: A Comparison In Decellularized Matrix Deposited By Synovium-Derived Stem Cells And Chondrocytes. J Tissue Sci Eng 2:104. doi:10.4172/2157-7552.1000104

Copyright: © 2010 Pei M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Objectives: Synovium-derived stem cells (SDSCs) are tissue-specific stem cells for chondrogenesis. Our aim was to evaluate whether decellularized matrix deposited by SDSCs was superior to chondrocytes in providing a stem cell microenvironment to conduct large scale expansion of high-quality cells for cartilage tissue engineering.
Materials and Methods: We generated two extracellular matrices (ECMs) deposited by either SDSCs (SECM) or chondrocytes (CECM). Passage 4 SDSCs and chondrocytes were expanded separately for two passages on three substrates: conventional plastic flasks (Plastic), SECM, or CECM. Expanded cells were incubated in a pellet culture system supplemented with serum-free chondrogenic medium for 14 days. Histology, biochemistry, real-time PCR, and western blot were used to evaluate expanded cell chondrogenic capacity.
Results: Cell proliferation was greatly improved during expansion on both ECMs, especially on SECM. ECM expansion enhanced cell chondrogenic potential, particularly for cells expanded on SECM. Collagen II and aggrecan were deposited only in CECM while collagen I and decorin existed in both ECMs. High levels of phospho-TGF-β receptor II found in chondrogenically induced cells after expansion on either ECM suggested that enhancement of chondrogenic potential might result from upregulated sensitivity in ECM-expanded cells when they are chondrogenically induced.
Conclusions: SECM is superior to CECM in promoting cell expansion and enhancing expanded cell chondrogenic potential. Decellularized stem cell matrix can serve as a novel cell expansion system for cartilage tissue engineering.

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