Diabetic pre-programming of myelopoiesis impairs tissue repair

J Pathol. 2020 Mar;250(3):245-247. doi: 10.1002/path.5370. Epub 2020 Jan 12.

Abstract

Bone marrow-derived monocyte-macrophages promote healing of injured tissue cooperatively with vasculogenic hematopoietic stem/progenitor cells. However, diabetes dysregulates hematopoiesis and attenuates bone marrow-derived tissue-reparative responses. In a recent issue of The Journal of Pathology, Barman et al extensively characterized myelopoietic responses in bone marrow following skin wounding in a type 2 model of diabetes. The study demonstrated that accumulation of monocyte-macrophages in the peripheral tissues is increased due to diabetic myelopoiesis that would oppose the reparative process following tissue injury. Interestingly, in this model, pathological myelopoiesis is independent of IL-1β. The potential prophylactic and therapeutic implications of these data are discussed in terms of paracrine signaling, macrophage polarization, and hematopoietic stem cell mobilization/retention. © 2019 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Keywords: diabetes; hematopoietic stem cells; myelopoiesis; tissue injury; vascular regeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Comment

MeSH terms

  • Diabetes Mellitus*
  • Hematopoiesis
  • Hematopoietic Stem Cells
  • Humans
  • Myelopoiesis*
  • United Kingdom