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Published Online: 30 June 2011

Stem Cells, Nitrogen-Rich Plasma-Polymerized Culture Surfaces, and Type X Collagen Suppression

Publication: Tissue Engineering Part A
Volume 17, Issue Number 19-20

Abstract

Mesenchymal stem cells (MSCs) are multipotent cells that can differentiate into chondrocytes, osteoblasts, myocytes, adipocytes, and a variety of other cell types. Several studies have been directed toward using MSCs from patients with osteoarthritis (OA) for cartilage repair, not only because these are the ones that will require a source of autologous stem cells if biological repair of cartilage lesions is to be a therapeutic option, but also to further an understanding of stem cell differentiation. Previous studies have shown that a major drawback of current cartilage and intervertebral disc tissue repair is that human MSCs from OA patients express type X collagen (COL X). COL X, a marker of late-stage chondrocyte hypertrophy, is implicated in endochondral ossification. However, those studies also revealed that a novel plasma-polymerized thin film material, named nitrogen-rich plasma-polymerized ethylene (PPE:N), was able to inhibit COL X expression in committed MSCs. The specific aim of this present study was to determine if the suppression of COL X by PPE:N is maintained when MSCs are transferred to pellet cultures in serum-free media. Our results confirmed the potential of two different types of PPE:N surfaces (low-pressure-PPE:N [L-PPE:N] and high-pressure-PPE:N [H-PPE:N]) in suppressing COL X expression, more so on the latter. Interestingly, when MSCs were transferred to pellet cultures, the expression level of COL X was further decreased by preincubation on H-PPE:N, suggesting that these kinds of coatings show promise for tissue engineering of cartilage and disc tissues. Further studies are needed to assess the relative importance of surface-chemistry versus surface-morphology in the mechanism of COL X suppression.

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cover image Tissue Engineering Part A
Tissue Engineering Part A
Volume 17Issue Number 19-20October 2011
Pages: 2551 - 2560
PubMed: 21599539

History

Published in print: October 2011
Published ahead of print: 5 July 2011
Published online: 30 June 2011
Published ahead of production: 20 May 2011
Accepted: 19 May 2011
Received: 15 December 2010

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Sonia Rampersad
Lady Davis Institute for Medical Research, SMBD-Jewish General Hospital, Montreal, Québec, Canada.
Division of Orthopaedic Surgery, McGill University, Montreal, Québec, Canada.
Juan-Carlos Ruiz
Department of Engineering Physics, École Polytechnique, Montreal, Québec, Canada.
Alain Petit
Lady Davis Institute for Medical Research, SMBD-Jewish General Hospital, Montreal, Québec, Canada.
Sophie Lerouge
Laboratory of Endovascular Biomaterials, Research Centre of the University of Montreal Hospital Centre (CRCHUM), Montreal, Québec, Canada.
John Antoniou
Lady Davis Institute for Medical Research, SMBD-Jewish General Hospital, Montreal, Québec, Canada.
Division of Orthopaedic Surgery, McGill University, Montreal, Québec, Canada.
Michael R. Wertheimer
Department of Engineering Physics, École Polytechnique, Montreal, Québec, Canada.
Fackson Mwale
Lady Davis Institute for Medical Research, SMBD-Jewish General Hospital, Montreal, Québec, Canada.
Division of Orthopaedic Surgery, McGill University, Montreal, Québec, Canada.

Notes

Address correspondence to:Fackson Mwale, Ph.D.Lady Davis Institute for Medical ResearchSMBD-Jewish General Hospital3755 Cote Ste-Catherine RoadMontrealQuébecCanada H3T 1E2
E-mail: [email protected]

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No competing financial interests exist.

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