Abstract

Aim:Mesenchymal stromal cells (MSC) are a promising tool for cellular therapy and regenerative medicine. One major difficulty in establishing a MSC expansion protocol is the large volume of bone marrow (BM) required. We studied whether cells trapped within a collection bag and filter system could be considered as a source of MSC.Results:From the 20 BM collection bag and filter systems, we recovered an average of 1.68 × 108 mononuclear cells, which is the equivalent to 60 ml of filtered BM. Mononuclear cells were expanded ex vivo to 17 × 106 MSC, with purity shown by a CD44+, CD105+, CD90+ and CD73+ immunophenotype, a reduction of 20% proliferating cells in a mixed lymphocyte reaction and also the ability of adipocyte differentiation.Conclusion:Long-term MSC cultures were established from the usually discarded BM collection bag and filter, maintaining an appropriate phenotype and function, being suitable for both investigation and clinical settings.

Highlights

  • Mesenchymal stromal cells (MSC) are a promising tool for both cellular therapy and regenerative medicine. Their ability to modulate the immune system in a HLA-independent manner makes every MSC donor a universal match

  • We describe here for the first time an alternative adipogenic media, relying on hospital pharmacy-available drugs capable of inducing adipogenesis

  • The routine recovery of such cells in reference HSCT centers could, in a way similar to a public cord-blood bank, benefit the scientific community

Read more

Summary

Objectives

Mesenchymal stromal cells (MSC) are a promising tool for cellular therapy and regenerative medicine. We aim to evaluate whether MNC can be isolated from the BM collection bag/filter and expanded ex vivo into functional MSC, with potential for post-transplant cellular therapy. We aim to expand MSC from the MNC recovered from the collection bag/filter system with an optimized protocol under GMP conditions and fully characterize the final product, performing trilineage differentiation and proliferation assays, in order to validate this as a source of MSC

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call