Experimental Hematology
Volume 38, Issue 7 , Pages 581-592, July 2010

Stem cell plasticity revisited: The continuum marrow model and phenotypic changes mediated by microvesicles

  • Peter J. Quesenberry

      Affiliations

    • Division of Hematology and Oncology, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI., USA
  • ,
  • Mark S. Dooner

      Affiliations

    • Division of Hematology and Oncology, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI., USA
  • ,
  • Jason M. Aliotta

      Affiliations

    • Division of Hematology and Oncology, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI., USA
    • Division of Pulmonary, Sleep and Critical Care Medicine, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI., USA
    • Corresponding Author InformationOffprint requests to: Jason M. Aliotta, M.D., Division of Hematology/Oncology, Rhode Island Hospital, 3rd Floor George Building, 593 Eddy Street, Providence, RI 02903

Received 27 February 2010; received in revised form 27 February 2010; accepted 31 March 2010. published online 12 April 2010.

The phenotype of marrow hematopoietic stem cells is determined by cell-cycle state and microvesicle entry into the stem cells. The stem cell population is continually changing based on cell-cycle transit and can only be defined on a population basis. Purification of marrow stem cells only addresses the heterogeneity of these populations. When whole marrow is studied, the long-term repopulating stem cells are in active cell cycle. However, with some variability, when highly purified stem cells are studied, the cells appear to be dormant. Thus, the study of purified stem cells is intrinsically misleading. Tissue-derived microvesicles enhanced by injury effect the phenotype of different cell classes. We propose that previously described stem cell plasticity is due to microvesicle modulation. We further propose a stem cell population model in which the individual cell phenotypes continually change, but the population phenotype is relatively stable. This, in turn, is modulated by microvesicle and microenvironmental influences.

 

PII: S0301-472X(10)00143-8

doi:10.1016/j.exphem.2010.03.021

Experimental Hematology
Volume 38, Issue 7 , Pages 581-592, July 2010