Hypersensitivity response has negligible impact on Hematopoietic Stem Cells

Stem Cell Reports. 2021 Aug 10;16(8):1884-1893. doi: 10.1016/j.stemcr.2021.06.013. Epub 2021 Jul 22.

Abstract

Immune cells are generated from hematopoietic stem cells (HSCs) in the bone marrow (BM). Immune stimulation can rapidly activate HSCs out of their quiescent state to accelerate the generation of immune cells. HSCs' activation follows various viral or bacterial stimuli, and we sought to investigate the hypersensitivity immune response. Surprisingly, the Ova-induced hypersensitivity peritonitis model finds no significant changes in BM HSCs. HSC markers cKIT, SCA1, CD48, CD150, and the Fgd5-mCherry reporter showed no significant difference from control. Functionally, hypersensitivity did not alter HSCs' potency, as assayed by transplantation. We further characterized the possible impact of hypersensitivity using RNA-sequencing of HSCs, finding minor changes at the transcriptome level. Moreover, hypersensitivity induced no significant change in the proliferative state of HSCs. Therefore, this study suggests that, in contrast to other immune stimuli, hypersensitivity has no impact on HSCs.

Keywords: dormancy; hematopoietic stem cells; hypersensitivity; immune response; quiescence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptive Immunity / immunology*
  • Animals
  • Ataxin-1 / genetics
  • Ataxin-1 / immunology
  • Ataxin-1 / metabolism
  • Bone Marrow Cells / immunology*
  • Bone Marrow Cells / metabolism
  • CD48 Antigen / genetics
  • CD48 Antigen / immunology
  • CD48 Antigen / metabolism
  • Cell Differentiation / genetics
  • Cell Differentiation / immunology
  • Hematopoietic Stem Cell Transplantation / methods
  • Hematopoietic Stem Cells / immunology*
  • Hematopoietic Stem Cells / metabolism
  • Hypersensitivity / immunology*
  • Mice
  • Mice, Congenic
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Proto-Oncogene Proteins c-kit / genetics
  • Proto-Oncogene Proteins c-kit / immunology
  • Proto-Oncogene Proteins c-kit / metabolism
  • RNA-Seq / methods
  • Transcriptome / genetics
  • Transcriptome / immunology*

Substances

  • Ataxin-1
  • Atxn1 protein, mouse
  • CD48 Antigen
  • Cd48 protein, mouse
  • Kit protein, mouse
  • Proto-Oncogene Proteins c-kit