Regulation of Drosophila hematopoietic sites by Activin-β from active sensory neurons

Nat Commun. 2017 Jul 27:8:15990. doi: 10.1038/ncomms15990.

Abstract

An outstanding question in animal development, tissue homeostasis and disease is how cell populations adapt to sensory inputs. During Drosophila larval development, hematopoietic sites are in direct contact with sensory neuron clusters of the peripheral nervous system (PNS), and blood cells (hemocytes) require the PNS for their survival and recruitment to these microenvironments, known as Hematopoietic Pockets. Here we report that Activin-β, a TGF-β family ligand, is expressed by sensory neurons of the PNS and regulates the proliferation and adhesion of hemocytes. These hemocyte responses depend on PNS activity, as shown by agonist treatment and transient silencing of sensory neurons. Activin-β has a key role in this regulation, which is apparent from reporter expression and mutant analyses. This mechanism of local sensory neurons controlling blood cell adaptation invites evolutionary parallels with vertebrate hematopoietic progenitors and the independent myeloid system of tissue macrophages, whose regulation by local microenvironments remain undefined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbachol / pharmacology
  • Cell Survival
  • Cellular Microenvironment
  • Cholinergic Agonists / pharmacology
  • Drosophila Proteins / drug effects
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / drug effects
  • Drosophila melanogaster / growth & development*
  • Drosophila melanogaster / metabolism
  • Hematopoiesis*
  • Hematopoietic System / drug effects
  • Hematopoietic System / metabolism*
  • Hemocytes / drug effects
  • Hemocytes / metabolism*
  • Inhibin-beta Subunits / metabolism*
  • Larva / drug effects
  • Larva / growth & development*
  • Larva / metabolism
  • Peripheral Nervous System / drug effects
  • Peripheral Nervous System / metabolism
  • Sensory Receptor Cells / drug effects
  • Sensory Receptor Cells / metabolism*

Substances

  • Cholinergic Agonists
  • Drosophila Proteins
  • Carbachol
  • Inhibin-beta Subunits