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Bone Marrow-Derived Progenitor Cells Mediate Immune Cell Regulation

  • Kisha N. SivanathanEmail author
  • Patrick T. Coates
Protocol
Part of the Methods in Molecular Biology book series (MIMB, volume 2029)

Abstract

Human bone marrow (BM) derived mesenchymal stem cells (MSC) have high capacity to propagate ex vivo with superior reparative, immunosuppressive, and anti-inflammatory properties. Here we describe standardized protocols and culture conditions that enable the isolation, expansion and maintenance of a highly purified and homogenous population of human MSC. These third party-derived off-the-shelf MSC from healthy human bone marrow donors can potently inhibit mitogenically or allogeneically activated human T cells in proliferation assays. The standard operating procedures described in this chapter can be applied to researchers aiming to enhance MSC immunosuppressive properties and defining MSC mechanisms of action. Importantly, these assays can be incorporated into clinical protocols where the safety and efficacy of human BM MSC can be verified in diseases that are modulated by T cell responses.

Key words

Mesenchymal stem cells Bone marrow T cells Peripheral blood mononuclear cells Bone marrow Proliferation assays Mixed lymphocyte reactions Mitogen Differentiation Immunophenotyping 

Notes

Acknowledgments

We thank all bone marrow donors and the Royal Adelaide Hospital, Adelaide, South Australia as well as the Australian Red Cross Blood Service for all the buffy coats. We would like to specially thank and acknowledge Svjetlana Kireta and Julie Johnston for their expertise, invaluable input throughout their long-term service in our laboratory at the University of Adelaide and Royal Adelaide Hospital and for proof-reading the manuscript. We thank the Australian Government and the National Health and Medical Council (NHMRC) for K.N.S CJ Martin Biomedical Postdoctoral Early Career Fellowship.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Faculty of Health and Medical Sciences, School of MedicineUniversity of AdelaideAdelaideAustralia
  2. 2.Evergrande Center for Immunologic DiseasesHarvard Medical School and Brigham and Women’s HospitalBostonUSA
  3. 3.Central Northern Adelaide Renal Transplantation ServiceRoyal Adelaide HospitalAdelaideAustralia

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