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Research Article

Non-multipotent stroma inhibit the proliferation and differentiation of mesenchymal stromal cells in vitro

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Pages 818-830 | Received 27 Nov 2009, Accepted 24 May 2010, Published online: 22 Jul 2010
 

Abstract

Background aims. The ability to expand and maintain bone marrow (BM)-derived mesenchymal stem cells (MSC) in vitro is an important aspect of their therapeutic potential. Despite this, the exact composition of stromal cell types within these cultures and the potential effects of non-stem cells on the maintenance of MSC are poorly understood. Methods. C57BL/6J BM stroma was investigated as a model to determine the relationship between MSC and non-multipotent cells in vitro. Whole BM and single-cell derived cultures were characterized using flow cytometry and cell sorting combined with multipotent differentiation. Proliferation of individual stromal populations was evaluated using BrdU. Results. At a single-cell level, MSC were distinguished from committed progenitors, and cells lacking differentiation ability, by the expression of CD105 (CD105+). A 3-fold reduction in the percentage of CD105+ cells was detected after prolonged culture and correlated with loss of MSC. Depletion of CD105+ cells coincided with a 10–20% increase in the frequency of proliferating CD105 cells. Removal of CD105 stroma caused increased proliferation in CD105+ cells, which could be diminished by conditioned media from parent cultures. Comparison of the multipotent differentiation potential in purified and non-purified CD105+ cells determined that MSC were detectable for at least 3 weeks longer when cultured in the absence of CD105 cells. Conclusions. This work identifies a simple model for characterizing the different cellular components present in BM stromal cultures and demonstrates that stromal cells lacking multipotent differentiating capacity greatly reduce the longevity of MSC.

Acknowledgements

We would like to acknowledge Paul Oleynik for operation of the MoFlo cell sorter, Dr Catherine Njue and Mr Jun Gao for assistance with statistical analysis, as well as Rudi Mueller and Pascale Bellon-Gagnon for their help with the cryosectioning and analysis of chondrocyte pellets. We would also like to thank Dr Richard Isbrucker, Dr Shiv Prasad and Dr Sean Li for their concise review of the manuscript. As well, we give deepest thanks to Dr Remy Aubin for assistance, guidance and critical comments during the completion of this work.

Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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