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Muscularis macrophage development in the absence of an enteric nervous system.

Marina Avetisyan | Julia E Rood | Silvia Huerta Lopez | Rajarshi Sengupta | Elizabeth Wright-Jin | Joseph D Dougherty | Edward M Behrens | Robert O Heuckeroth
Proceedings of the National Academy of Sciences of the United States of America | 2018

The nervous system of the bowel regulates the inflammatory phenotype of tissue resident muscularis macrophages (MM), and in adult mice, enteric neurons are the main local source of colony stimulating factor 1 (CSF1), a protein required for MM survival. Surprisingly, we find that during development MM colonize the bowel before enteric neurons. This calls into question the requirement for neuron-derived CSF1 for MM colonization of the bowel. To determine if intestinal innervation is required for MM development, we analyzed MM of neonatal Ret-/- (Ret KO) mice that have no enteric nervous system in small bowel or colon. We found normal numbers of well-patterned MM in Ret KO bowel. Similarly, the abundance and distribution of MM in aganglionic human colon obtained from Hirschsprung disease patients was normal. We also identify endothelial cells and interstitial cells of Cajal as the main sources of CSF1 in the developing bowel. Additionally, MM from neonatal Ret KOs do not differ from controls in baseline activation status or cytokine-production in response to lipopolysaccharide. Unexpectedly, these data demonstrate that the enteric nervous system is dispensable for MM colonization and patterning in the bowel, and suggest that modulatory interactions between MM and the bowel nervous system are established postnatally.

Pubmed ID: 29666241

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Associated grants

  • Agency: NIH HHS, United States
    Id: OT2 OD023859
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK050306
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK087715
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS102272

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Rettm1Jmi/Rettm1Jmi (organism)

RRID:MGI:3623107

Allele Detail: Targeted This is a legacy resource.

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