Neutralizing negative epigenetic regulation by HDAC5 enhances human haematopoietic stem cell homing and engraftment

Nat Commun. 2018 Jul 16;9(1):2741. doi: 10.1038/s41467-018-05178-5.

Abstract

Enhancement of hematopoietic stem cell (HSC) homing and engraftment is clinically critical, especially for cord blood (CB) hematopoietic cell transplantation. Here we report that specific HDAC5 inhibition highly upregulates CXCR4 surface expression in human CB HSCs and progenitor cells (HPCs). This results in enhanced SDF-1/CXCR4-mediated chemotaxis and increased homing to the bone marrow environment, with elevated SCID-repopulating cell (SRC) frequency and enhanced long-term and secondary engraftment in NSG mice. HDAC5 inhibition increases acetylated p65 levels in the nucleus, which is important for CXCR4 transcription. Inhibition of nuclear factor-κB (NF-κB) signaling suppresses HDAC5-mediated CXCR4 upregulation, enhanced HSC homing, and engraftment. Furthermore, activation of the NF-κB signaling pathway via TNFα also results in significantly increased CXCR4 surface expression, enhanced HSC homing, and engraftment. These results demonstrate a previously unknown negative epigenetic regulation of HSC homing and engraftment by HDAC5, and allow for a new and simple translational strategy to enhance HSC transplantation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chemokine CXCL12 / genetics*
  • Chemokine CXCL12 / immunology
  • Chemotaxis
  • Cord Blood Stem Cell Transplantation*
  • Epigenesis, Genetic*
  • Fetal Blood / cytology
  • Fetal Blood / drug effects
  • Fetal Blood / immunology*
  • Graft Survival*
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / immunology
  • Histone Deacetylases / genetics*
  • Histone Deacetylases / immunology
  • Humans
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Primary Cell Culture
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / immunology
  • Signal Transduction
  • Transcription Factor RelA / genetics
  • Transcription Factor RelA / immunology
  • Transplantation, Heterologous
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • CXCL12 protein, human
  • CXCR4 protein, human
  • Chemokine CXCL12
  • RNA, Small Interfering
  • Receptors, CXCR4
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • HDAC5 protein, human
  • Histone Deacetylases