Cartilage regeneration by chondrogenic induced adult stem cells in osteoarthritic sheep model.

PLoS One

Tissue Engineering Centre, Universiti Kebangsaan Malaysia Medical Centre, Cheras, Selangor, Malaysia; Department of Physiology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Selangor, Malaysia.

Published: June 2015

AI Article Synopsis

  • The study explored the use of adipose stem cells (ADSC) and bone marrow stem cells (BMSC) for regenerating cartilage in a sheep model with surgically induced osteoarthritis.
  • After inducing osteoarthritis in sheep, the researchers injected chondrogenically induced stem cells into the affected knee joints, while control sheep received culture medium.
  • Results showed that both cell types promoted cartilage regeneration, with ADSCs proliferating faster but BMSCs exhibiting stronger gene expression for cartilage formation, indicating their potential for treating osteoarthritis.

Article Abstract

Objectives: In this study, Adipose stem cells (ADSC) and bone marrow stem cells (BMSC), multipotent adult cells with the potentials for cartilage regenerations were induced to chondrogenic lineage and used for cartilage regenerations in surgically induced osteoarthritis in sheep model.

Methods: Osteoarthritis was induced at the right knee of sheep by complete resection of the anterior cruciate ligament and medial meniscus following a 3-weeks exercise regimen. Stem cells from experimental sheep were culture expanded and induced to chondrogenic lineage. Test sheep received a single dose of 2 × 10(7) autologous PKH26-labelled, chondrogenically induced ADSCs or BMSCs as 5 mls injection, while controls received 5 mls culture medium.

Results: The proliferation rate of ADSCs 34.4 ± 1.6 hr was significantly higher than that of the BMSCs 48.8 ± 5.3 hr (P = 0.008). Chondrogenic induced BMSCs had significantly higher expressions of chondrogenic specific genes (Collagen II, SOX9 and Aggrecan) compared to chondrogenic ADSCs (P = 0.031, 0.010 and 0.013). Grossly, the treated knee joints showed regenerated de novo cartilages within 6 weeks post-treatment. On the International Cartilage Repair Society grade scores, chondrogenically induced ADSCs and BMSCs groups had significantly lower scores than controls (P = 0.0001 and 0.0001). Fluorescence of the tracking dye (PKH26) in the injected cells showed that they had populated the damaged area of cartilage. Histological staining revealed loosely packed matrixes of de novo cartilages and immunostaining demonstrated the presence of cartilage specific proteins, Collagen II and SOX9.

Conclusion: Autologous chondrogenically induced ADSCs and BMSCs could be promising cell sources for cartilage regeneration in osteoarthritis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049590PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0098770PLOS

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