TY - JOUR
T1 - Unique Neural Circuit Connectivity of Mouse Proximal, Middle, and Distal Colon Defines Regional Colonic Motor Patterns
AU - Nestor-Kalinoski, Andrea
AU - Smith-Edwards, Kristen M.
AU - Meerschaert, Kimberly
AU - Margiotta, Joseph F.
AU - Rajwa, Bartek
AU - Davis, Brian M.
AU - Howard, Marthe J.
N1 - Funding Information:
The authors thank Ms Samantha McKee, Dr Kalina Hristova-Venkova, and Dr Alexander Hristov for excellent technical support and animal husbandry. Calca-EGFP, FG104 mice Tg(Calca-EGFP)FG104Gsat, and CGRPA reporter mice were a generous gift from Dr David Ginty (Department of Neurobiology, Harvard Medical School). Tyrosine receptor kinase B CreERT2 mice, originally provided by Dr David Ginty, were crossed with mice containing a fusion protein of channelrhodopsin-2 and EYFP in the Rosa26 locus downstream of a floxed STOP cassette to generate tyrosine receptor kinase B–ChR2–YFP mice; tissues from these mice were generously provided by Dr Richard Koerber (Department of Neurobiology, School of Medicine, University of Pittsburgh). Hu ANNA-1 (HuC/D) was a generous gift from Dr Vanda A. Lennon (Neuroimmunology Laboratory, Mayo Clinic). The RNA sequencing BAM and FastQ files will be available through the National Institutes of Health Stimulating Peripheral Activity to Relieve Conditions Portal (RRID: SCR_017041) under a CC-BY 4.0 license at: https://doi.org/10.26275/sfbw-ax7q. Andrea Nestor-Kalinoski, PhD (Investigation: Equal; Methodology: Supporting; Resources: Equal; Visualization: Equal; Writing – review & editing: Equal), Kristen M Smith-Edwards, PhD (Formal analysis: Supporting; Investigation: Supporting; Methodology: Equal; Resources: Equal; Writing – review & editing: Equal), Kimberly Meerschaert, BS (Investigation: Equal; Methodology: Equal), Joseph F Margiotta, PhD (Data curation: Equal; Formal analysis: Equal; Investigation: Equal; Methodology: Equal; Resources: Equal; Software: Equal; Validation: Equal; Visualization: Equal; Writing – review & editing: Equal), Bartek Rajwa, PhD (Investigation: Supporting; Methodology: Equal; Resources: Supporting; Writing – review & editing: Equal), Brian M Davis, PhD (Investigation: Equal; Methodology: Equal; Resources: Supporting; Supervision: Equal; Writing – review & editing: Equal), Marthe J Howard, Ph.D. (Conceptualization: Lead; Data curation: Lead; Formal analysis: Lead; Funding acquisition: Lead; Investigation: Lead; Methodology: Equal; Project administration: Lead; Resources: Equal; Supervision: Lead; Validation: Equal; Visualization: Lead; Writing – original draft: Lead; Writing – review & editing: Equal). Funding This work was supported by the National Institutes of Health, Stimulating Peripheral Activity to Relieve Conditions (SPARC) program as an Other Transactions award, OT2OD023859 (PI: Marthe J. Howard; Co-Is Joseph F. Margiotta, Andrea Kalinoski, Brian M. Davis and NIBIB U18EB021790 (PI: Marthe J. Howard, and NIH Other Transaction award OT2OD023847 (PI: Bartek Rajwa) and The National Institutes of Health grant NIDDK122798 (PI: Brian M. Davis; CoPI: Marthe J. Howard).
Publisher Copyright:
© 2022 The Authors
PY - 2022/1
Y1 - 2022/1
N2 - Background & Aims: Colonic motor patterns have been described by a number of different groups, but the neural connectivity and ganglion architecture supporting patterned motor activity have not been elucidated. Our goals were to describe quantitatively, by region, the structural architecture of the mouse enteric nervous system and use functional calcium imaging, pharmacology, and electrical stimulation to show regional underpinnings of different motor patterns. Methods: Excised colon segments from mice expressing the calcium indicator GCaMP6f or GCaMP6s were used to examine spontaneous and evoked (pharmacologic or electrical) changes in GCaMP-mediated fluorescence and coupled with assessment of colonic motor activity, immunohistochemistry, and confocal imaging. Three-dimensional image reconstruction and statistical methods were used to describe quantitatively mouse colon myenteric ganglion structure, neural and vascular network patterning, and neural connectivity. Results: In intact colon, regionally specific myenteric ganglion size, architecture, and neural circuit connectivity patterns along with neurotransmitter-receptor expression underlie colonic motor patterns that define functional differences along the colon. Region-specific effects on spontaneous, evoked, and chemically induced neural activity contribute to regional motor patterns, as does intraganglionic functional connectivity. We provide direct evidence of neural circuit structural and functional regional differences that have only been inferred in previous investigations. We include regional comparisons between quantitative measures in mouse and human colon that represent an important advance in showing the usefulness and relevance of the mouse system for translation to the human colon. Conclusions: There are several neural mechanisms dependent on myenteric ganglion architecture and functional connectivity that underlie neurogenic control of patterned motor function in the mouse colon.
AB - Background & Aims: Colonic motor patterns have been described by a number of different groups, but the neural connectivity and ganglion architecture supporting patterned motor activity have not been elucidated. Our goals were to describe quantitatively, by region, the structural architecture of the mouse enteric nervous system and use functional calcium imaging, pharmacology, and electrical stimulation to show regional underpinnings of different motor patterns. Methods: Excised colon segments from mice expressing the calcium indicator GCaMP6f or GCaMP6s were used to examine spontaneous and evoked (pharmacologic or electrical) changes in GCaMP-mediated fluorescence and coupled with assessment of colonic motor activity, immunohistochemistry, and confocal imaging. Three-dimensional image reconstruction and statistical methods were used to describe quantitatively mouse colon myenteric ganglion structure, neural and vascular network patterning, and neural connectivity. Results: In intact colon, regionally specific myenteric ganglion size, architecture, and neural circuit connectivity patterns along with neurotransmitter-receptor expression underlie colonic motor patterns that define functional differences along the colon. Region-specific effects on spontaneous, evoked, and chemically induced neural activity contribute to regional motor patterns, as does intraganglionic functional connectivity. We provide direct evidence of neural circuit structural and functional regional differences that have only been inferred in previous investigations. We include regional comparisons between quantitative measures in mouse and human colon that represent an important advance in showing the usefulness and relevance of the mouse system for translation to the human colon. Conclusions: There are several neural mechanisms dependent on myenteric ganglion architecture and functional connectivity that underlie neurogenic control of patterned motor function in the mouse colon.
KW - Colonic Enteric Nervous System
KW - Functional Neural Circuitry
KW - Gastrointestinal
KW - Quantitative Morphology
UR - http://www.scopus.com/inward/record.url?scp=85119209373&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85119209373&partnerID=8YFLogxK
U2 - 10.1016/j.jcmgh.2021.08.016
DO - 10.1016/j.jcmgh.2021.08.016
M3 - Article
C2 - 34509687
AN - SCOPUS:85119209373
SN - 2352-345X
VL - 13
SP - 309-337.e3
JO - Cellular and Molecular Gastroenterology and Hepatology
JF - Cellular and Molecular Gastroenterology and Hepatology
IS - 1
ER -