Nociceptive nerves regulate haematopoietic stem cell mobilization

Nature. 2021 Jan;589(7843):591-596. doi: 10.1038/s41586-020-03057-y. Epub 2020 Dec 23.

Abstract

Haematopoietic stem cells (HSCs) reside in specialized microenvironments in the bone marrow-often referred to as 'niches'-that represent complex regulatory milieux influenced by multiple cellular constituents, including nerves1,2. Although sympathetic nerves are known to regulate the HSC niche3-6, the contribution of nociceptive neurons in the bone marrow remains unclear. Here we show that nociceptive nerves are required for enforced HSC mobilization and that they collaborate with sympathetic nerves to maintain HSCs in the bone marrow. Nociceptor neurons drive granulocyte colony-stimulating factor (G-CSF)-induced HSC mobilization via the secretion of calcitonin gene-related peptide (CGRP). Unlike sympathetic nerves, which regulate HSCs indirectly via the niche3,4,6, CGRP acts directly on HSCs via receptor activity modifying protein 1 (RAMP1) and the calcitonin receptor-like receptor (CALCRL) to promote egress by activating the Gαs/adenylyl cyclase/cAMP pathway. The ingestion of food containing capsaicin-a natural component of chili peppers that can trigger the activation of nociceptive neurons-significantly enhanced HSC mobilization in mice. Targeting the nociceptive nervous system could therefore represent a strategy to improve the yield of HSCs for stem cell-based therapeutic agents.

Publication types

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

MeSH terms

  • Adenylyl Cyclases / metabolism
  • Animals
  • Autonomic Pathways* / drug effects
  • Calcitonin Gene-Related Peptide / metabolism
  • Calcitonin Receptor-Like Protein / metabolism
  • Capsaicin / pharmacology
  • Cell Movement* / drug effects
  • Cyclic AMP / metabolism
  • Female
  • GTP-Binding Protein alpha Subunits, Gs / metabolism
  • Granulocyte Colony-Stimulating Factor / metabolism
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nociception / drug effects
  • Nociception / physiology*
  • Nociceptors / drug effects
  • Nociceptors / physiology*
  • Receptor Activity-Modifying Protein 1 / metabolism
  • Signal Transduction / drug effects
  • Stem Cell Niche
  • Sympathetic Nervous System / cytology*
  • Sympathetic Nervous System / drug effects

Substances

  • Calcitonin Receptor-Like Protein
  • Calcrl protein, mouse
  • Ramp1 protein, mouse
  • Receptor Activity-Modifying Protein 1
  • Granulocyte Colony-Stimulating Factor
  • Cyclic AMP
  • GTP-Binding Protein alpha Subunits, Gs
  • Adenylyl Cyclases
  • Calcitonin Gene-Related Peptide
  • Capsaicin