A Molecular Basis for Macrophage Control of Enteric Nervous System Function

dc.contributor.advisorReese, Tiffany A.en
dc.contributor.committeeMemberHooper, Lora V.en
dc.contributor.committeeMemberKliewer, Steven A.en
dc.contributor.committeeMemberChen, Zhijian J.en
dc.creatorPendse, Mihir Vidyadharen
dc.creator.orcid0000-0002-7810-6791
dc.date.accessioned2024-06-07T19:15:15Z
dc.date.available2024-06-07T19:15:15Z
dc.date.created2022-05
dc.date.issued2022-05
dc.date.submittedMay 2022
dc.date.updated2024-06-07T19:15:15Z
dc.description.abstractPeristaltic movement of the intestine propels food down the length of the gastrointestinal tract to promote nutrient absorption. Interactions between intestinal macrophages and the enteric nervous system regulate gastrointestinal motility, yet we have an incomplete understanding of the molecular mediators of this crosstalk. Here we identify complement component 1q (C1q) as a macrophage product that regulates gut motility. Macrophages were the predominant source of C1q in the mouse intestine and most extraintestinal tissues. Although C1q mediates complement-mediated killing of bacteria in the bloodstream, we found that C1q was not essential for immune defense of the intestine. Instead, C1q-expressing macrophages were localized to the intestinal submucosal plexus where they closely associated with enteric neurons and expressed surface markers characteristic of nerve-adjacent macrophages in other tissues. Mice with a macrophage-specific deletion of C1qa showed changes in enteric neuronal gene expression, increased peristaltic activity, and accelerated intestinal transit. Our findings identify C1q as a key regulator of gastrointestinal motility and provide enhanced insight into the crosstalk between macrophages and the enteric nervous system.en
dc.format.mimetypeapplication/pdfen
dc.identifier.oclc1438579290
dc.identifier.urihttps://hdl.handle.net/2152.5/10303
dc.language.isoenen
dc.subjectComplement C1qen
dc.subjectEnteric Nervous Systemen
dc.subjectMacrophagesen
dc.titleA Molecular Basis for Macrophage Control of Enteric Nervous System Functionen
dc.typeThesisen
dc.type.materialtexten
local.embargo.lift2024-06-01
local.embargo.terms2024-06-01
thesis.degree.departmentGraduate School of Biomedical Sciencesen
thesis.degree.disciplineImmunologyen
thesis.degree.grantorUT Southwestern Medical Centeren
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophyen

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