## Abstract The purpose of this study was the assessment of clinical, biochemical, and histologic effects of intraarticular administered adiposeโderived stromal vascular fraction or bone marrowโderived mesenchymal stem cells for treatment of osteoarthritis. Osteoarthritis was induced arthroscopical
Biologic properties of mesenchymal stem cells derived from bone marrow and adipose tissue
โ Scribed by Reza Izadpanah; Cynthia Trygg; Bindiya Patel; Christopher Kriedt; Jason Dufour; Jeffery M. Gimble; Bruce A. Bunnell
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 377 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
The biologic characteristics of mesenchymal stem cells (MSCs) isolated from two distinct tissues, bone marrow and adipose tissue were evaluated in these studies. MSCs derived from human and nonโhuman primate (rhesus monkey) tissue sources were compared. The data indicate that MSCs isolated from rhesus bone marrow (rBMSCs) and human adipose tissue (hASCs) had more similar biologic properties than MSCs of rhesus adipose tissue (rASCs) and human bone marrow MSCs (hBMSCs). Analyses of in vitro growth kinetics revealed shorter doubling time for rBMSCs and hASCs. rBMSCs and hASCs underwent significantly more population doublings than the other MSCs. MSCs from all sources showed a marked decrease in telomerase activity over extended culture; however, they maintained their mean telomere length. All of the MSCs expressed embryonic stem cell markers, Octโ4, Rexโ1, and Soxโ2 for at least 10 passages. Early populations of MSCs types showed similar multilineage differentiation capability. However, only the rBMSCs and hASCs retain greater differentiation efficiency at higher passages. Overall in vitro characterization of MSCs from these two species and tissue sources revealed a high level of common biologic properties. However, the results demonstrate clear biologic distinctions, as well. J. Cell. Biochem. 99: 1285โ1297, 2006. ยฉ 2006 WileyโLiss, Inc.
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