Manipulation of Hematopoietic Stem Cell Fate by Small Molecule Compounds

Stem Cells Dev. 2018 Sep 1;27(17):1175-1190. doi: 10.1089/scd.2018.0091. Epub 2018 Aug 22.

Abstract

Self-renewal and multipotential differentiation are two important features of hematopoietic stem/progenitor cells (HS/PCs) that make them as an ideal source of stem cells for treatment of many hematologic disorders and cancers. Regarding the limited number of cord blood HS/PCs, proper ex vivo expansion can significantly increase the clinical use of cord blood stem cells. Meanwhile, expansion of HS/PCs will be feasible through bypassing the quiescent state of HS/PCs and simultaneously enhancing their proliferative potential and survival while delaying the terminal differentiation and exhaustion. Previous investigations have demonstrated that defined sets of exogenous hematopoietic cytokines/growth factors such as stem cell factor, Flt-3 ligand, and thrombopoietin are able to expand HS/PCs. However, in recent years, small molecule compounds (SMCs) have emerged as a powerful tool for the effective expansion of HS/PCs by modulating multiple cellular processes including different signaling pathways and epigenetics. In this review, recent progress toward the use of SMCs in HS cell research is presented. We focus on the significant applications of SMCs related to HS/PC expansion and discuss the associated mechanism. At the end we present a list of those SMCs which enter to clinical trials.

Keywords: ex vivo expansion; hematopoietic stem/progenitor cells; small molecule compounds; umbilical cord blood.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Cycle / drug effects
  • Cell Cycle / genetics
  • Cell Differentiation / drug effects*
  • Cell Differentiation / genetics
  • Cell Division / drug effects
  • Cell Division / genetics
  • Cell Proliferation / drug effects*
  • Cell Proliferation / genetics
  • Cells, Cultured
  • Gene Expression / drug effects
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / metabolism
  • Humans
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Small Molecule Libraries / classification
  • Small Molecule Libraries / pharmacology*

Substances

  • Small Molecule Libraries