Muscularis macrophage development in the absence of an enteric nervous system

被引:63
|
作者
Avetisyan, Marina [1 ,2 ,3 ]
Rood, Julia E. [4 ,5 ]
Lopez, Silvia Huerta [1 ,2 ]
Sengupta, Rajarshi [1 ,2 ]
Wright-Jin, Elizabeth [6 ]
Dougherty, Joseph D. [7 ,8 ]
Behrens, Edward M. [4 ,5 ]
Heuckeroth, Robert O. [1 ,2 ]
机构
[1] Childrens Hosp Philadelphia, Res Inst, Abramson Res Ctr, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[4] Childrens Hosp Philadelphia, Abramson Res Ctr, Div Rheumatol, Philadelphia, PA 19104 USA
[5] Univ Penn, Perelman Sch Med, Inst Immunol, Philadelphia, PA 19104 USA
[6] Washington Univ, Sch Med, Dept Pediat Neurol, St Louis, MO 63110 USA
[7] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[8] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
关键词
muscularis macrophages; enteric nervous system; neuroimmunology; Hirschsprung disease; Ret; MOUSE SMALL-INTESTINE; NEURAL CREST; POSTNATAL-DEVELOPMENT; HIRSCHSPRUNG DISEASE; GASTROINTESTINAL MOTILITY; DIABETIC GASTROPARESIS; INTERSTITIAL-CELLS; RET; EXTERNA; NEURONS;
D O I
10.1073/pnas.1802490115
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:4696 / 4701
页数:6
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