Selection of Cell Source for Ligament Tissue Engineering
Use of appropriate types of cells could potentially improve the functionality and structure of tissue engineered constructs, but little is known about the optimal cell source for ligament tissue engineering. The object of this study was to determine the optimal cell source for anterior cruciate liga...
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2005-09-01
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Series: | Cell Transplantation |
Online Access: | https://doi.org/10.3727/000000005783982819 |
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doaj-9d27ef18210e446ca1b03c8ed6b5933c2020-11-25T02:48:08ZengSAGE PublishingCell Transplantation0963-68971555-38922005-09-011410.3727/000000005783982819Selection of Cell Source for Ligament Tissue EngineeringZigang Ge0James Cho Hong Goh Ph.D.1Eng Hin Lee2Department of Orthopaedic Surgery, National University of Singapore, Singapore, 119260Division of Bioengineering, National University of Singapore, Singapore, 119260Department of Orthopaedic Surgery, National University of Singapore, Singapore, 119260Use of appropriate types of cells could potentially improve the functionality and structure of tissue engineered constructs, but little is known about the optimal cell source for ligament tissue engineering. The object of this study was to determine the optimal cell source for anterior cruciate ligament (ACL) tissue engineering. Fibroblasts isolated from anterior cruciate ligament, medial collateral ligament (MCL), as well as bone marrow mesenchymal stem cells (MSC) were compared using the following parameters: proliferation rate, collagen excretion, expression of collagen type I, II, and III, as well as α-smooth muscle actin. Green fluorescent protein (GFP) transfected MSCs were used to trace their fate in the knee joints. MSC, ACL, and MCL fibroblasts were all highly stained with antibodies for collagen types I and III and α-smooth muscle actin while negatively stained with collagen type II. Proliferation rate and collagen excretion of MSCs were higher than ACL and MCL fibroblasts (p < 0.05), and MSCs could survive for at least 6 weeks in knee joints. In summary, MSC is potentially a better cell source than ACL and MCL fibroblasts for anterior cruciate ligament tissue engineering.https://doi.org/10.3727/000000005783982819 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zigang Ge James Cho Hong Goh Ph.D. Eng Hin Lee |
spellingShingle |
Zigang Ge James Cho Hong Goh Ph.D. Eng Hin Lee Selection of Cell Source for Ligament Tissue Engineering Cell Transplantation |
author_facet |
Zigang Ge James Cho Hong Goh Ph.D. Eng Hin Lee |
author_sort |
Zigang Ge |
title |
Selection of Cell Source for Ligament Tissue Engineering |
title_short |
Selection of Cell Source for Ligament Tissue Engineering |
title_full |
Selection of Cell Source for Ligament Tissue Engineering |
title_fullStr |
Selection of Cell Source for Ligament Tissue Engineering |
title_full_unstemmed |
Selection of Cell Source for Ligament Tissue Engineering |
title_sort |
selection of cell source for ligament tissue engineering |
publisher |
SAGE Publishing |
series |
Cell Transplantation |
issn |
0963-6897 1555-3892 |
publishDate |
2005-09-01 |
description |
Use of appropriate types of cells could potentially improve the functionality and structure of tissue engineered constructs, but little is known about the optimal cell source for ligament tissue engineering. The object of this study was to determine the optimal cell source for anterior cruciate ligament (ACL) tissue engineering. Fibroblasts isolated from anterior cruciate ligament, medial collateral ligament (MCL), as well as bone marrow mesenchymal stem cells (MSC) were compared using the following parameters: proliferation rate, collagen excretion, expression of collagen type I, II, and III, as well as α-smooth muscle actin. Green fluorescent protein (GFP) transfected MSCs were used to trace their fate in the knee joints. MSC, ACL, and MCL fibroblasts were all highly stained with antibodies for collagen types I and III and α-smooth muscle actin while negatively stained with collagen type II. Proliferation rate and collagen excretion of MSCs were higher than ACL and MCL fibroblasts (p < 0.05), and MSCs could survive for at least 6 weeks in knee joints. In summary, MSC is potentially a better cell source than ACL and MCL fibroblasts for anterior cruciate ligament tissue engineering. |
url |
https://doi.org/10.3727/000000005783982819 |
work_keys_str_mv |
AT zigangge selectionofcellsourceforligamenttissueengineering AT jameschohonggohphd selectionofcellsourceforligamenttissueengineering AT enghinlee selectionofcellsourceforligamenttissueengineering |
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