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Mesenchymal Stromal Cells

Impaired differentiation potential of human trabecular bone mesenchymal stromal cells from elderly patients

, , , , , , , & show all
Pages 584-594 | Published online: 16 Sep 2009
 

Abstract

Background aims

Advances in bone tissue engineering with mesenchymal stromal cells (MSC) as an alternative to conventional orthopedic procedures has opened new horizons for the treatment of large bone defects. Bone marrow (BM) and trabecular bone are both sources of MSC. Regarding clinical use, we tested the potency of MSC from different sources.

Methods

We obtained MSC from 17 donors (mean age 64.6 years) by extensive washing of trabecular bone from the femoral head and trochanter, as well as BM aspirates of the iliac crest and trochanter. The starting material was evaluated by histologic analysis and assessment of colony-forming unit–fibroblasts (CFU-F). The MSC populations were compared for proliferation and differentiation potential, at RNA and morphologic levels.

Results

MSC proliferation potential and immunophenotype (expression of CD49a, CD73, CD90, CD105, CD146 and Stro-1) were similar whatever the starting material. However, the differentiation potential of MSC obtained by bone washing was impaired compared with aspiration; culture-amplified cells showed few Oil Red O-positive adipocytes and few mineralized areas and formed inconsistent Alcian blue-positive high-density micropellets after growth under adipogenic, osteogenic and chondrogenic conditions, respectively. MSC cultured with 1 ng/mL fibroblast growth factor 2 (FGF-2) showed better differentiation potential.

Conclusions

Trabecular bone MSC from elderly patients is not good starting material for use in cell therapy for bone repair and regeneration, unless cultured in the presence of FGF-2.

Acknowledgements

This research was supported by the integrated project Genostem of the European Commission FP6 research funding program and by grant number 2004-08 from the Etablissement Français du Sang. The authors thank Jean-Louis Brémond for histologic analysis of bone marrow biopsies and James E. Dennis for a critical review of the manuscript.

Declaration of interest: No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article.

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