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Engineered cartilage tissue from biodegradable Poly(ε-caprolactone) scaffold and human umbilical cord derived mesenchymal stem cells

Phuc Dang-Ngoc Nguyen 1
Ngoc Bich Vu 1, 2, * ORCID logo
Ha Thi-Ngan Le 1, 2
Thuy Thi-Thanh Dao 1, 2
Long Xuan Gia 3
Phuc Van Pham 1, 2, 4 ORCID logo
  1. Stem Cell Institute, University of Science, VNUHCM, Ho Chi Minh City, Vietnam
  2. Laboratory of Stem Cell Research and Application, University of Science, VNUHCM, Ho Chi Minh City, Vietnam
  3. Institute of Applied Mechanics and Informatics - Vietnam Academy of Science and Technology, Viet Nam
  4. Faculty of Biology and Biotechnology, University of Science, VNUHCM, Ho Chi Minh city, Vietnam
Correspondence to: Ngoc Bich Vu, Stem Cell Institute, University of Science, VNUHCM, Ho Chi Minh City, Vietnam; Laboratory of Stem Cell Research and Application, University of Science, VNUHCM, Ho Chi Minh City, Vietnam. ORCID: https://orcid.org/0000-0003-4447-9212. Email: ngocvu@sci.edu.vn.
Volume & Issue: Vol. 5 No. 02 (2018) | Page No.: 2000-2012 | DOI: 10.15419/bmrat.v5i02.414
Published: 2018-02-26

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This article is published with open access by BioMedPress. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. 

Abstract

Introduction: Cartilage injury is the most common injury among orthopedic diseases. The predominant treatment for this condition is cartilage transplantation. Therefore, production of cartilage for treatment is an important strategy in regenerative medicine of cartilage to provide surgeons with an additional option for treatment of cartilage defects. This study aimed to produce in vitro engineered cartilage tissue by culturing and differentiating umbilical cord derived mesenchymal stem cells on biodegradable Poly(ε-caprolactone) (PCL) scaffold.

Methods: Human umbilical cord derived mesenchymal stem cells (UCMSCs) were isolated and expanded according to previous published protocols. UCMSCs were labeled with CD90 APC‑conjugated monoclonal antibody (CD90-APC) and then seeded onto porous PCL scaffolds. Cell adhesion and proliferation on PCL scaffolds were evaluated based on the strength/signal of APC, MTT assays, and scanning electron microscopy (SEM). The chondrogenic differentiation of UCMSCs on scaffolds was detected by Alcian Blue and Safranin O staining.

Results: The results showed that UCMSCs successfully adhered, proliferated and differentiated into chondroblasts and chondrocytes on PCL scaffolds. The chondrocyte scaffolds were positive for some markers of cartilage, as indicated by Alcian Blue and Safranin O staining.

Conclusion: In conclusion, this study showed successful production of cartilage tissues from UCMSCs on PCL scaffolds.

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