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      Regional complexity in enteric neuron wiring reflects diversity of motility patterns in the mouse large intestine

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          Abstract

          The enteric nervous system controls a variety of gastrointestinal functions including intestinal motility. The minimal neuronal circuit necessary to direct peristalsis is well-characterized but several intestinal regions display also other motility patterns for which the underlying circuits and connectivity schemes that coordinate the transition between those patterns are poorly understood. We investigated whether in regions with a richer palette of motility patterns, the underlying nerve circuits reflect this complexity. Using Ca 2+ imaging, we determined the location and response fingerprint of large populations of enteric neurons upon focal network stimulation. Complemented by neuronal tracing and volumetric reconstructions of synaptic contacts, this shows that the multifunctional proximal colon requires specific additional circuit components as compared to the distal colon, where peristalsis is the predominant motility pattern. Our study reveals that motility control is hard-wired in the enteric neural networks and that circuit complexity matches the motor pattern portfolio of specific intestinal regions.

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          Most cited references62

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          Types of neurons in the enteric nervous system.

          This paper, written for the symposium in honour of more than 40 years' contribution to autonomic research by Professor Geoffrey Burnstock, highlights the progress made in understanding the organisation of the enteric nervous system over this time. Forty years ago, the prevailing view was that the neurons within the gut wall were post-ganglionic neurons of parasympathetic pathways. This view was replaced as evidence accrued that the neurons are part of the enteric nervous system and are involved in reflex and integrative activities that can occur even in the absence of neuronal influence from extrinsic sources. Work in Burnstock's laboratory led to the discovery of intrinsic inhibitory neurons with then novel pharmacology of transmission, and precipitated investigation of neuron types in the enteric nervous system. All the types of neurons in the enteric nervous system of the small intestine of the guinea-pig have now been identified in terms of their morphologies, projections, primary neurotransmitters and physiological identification. In this region there are 14 functionally defined neuron types, each with a characteristic combination of morphological, neurochemical and biophysical properties. The nerve circuits underlying effects on motility, blood flow and secretion that are mediated through the enteric nervous system are constructed from these neurons. The circuits for simple motility reflexes are now known, and progress has been made in analysing those involved in local control of blood flow and transmucosal fluid movement in the small intestine.
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            A Cre-dependent GCaMP3 reporter mouse for neuronal imaging in vivo.

            Fluorescent calcium indicator proteins, such as GCaMP3, allow imaging of activity in genetically defined neuronal populations. GCaMP3 can be expressed using various gene delivery methods, such as viral infection or electroporation. However, these methods are invasive and provide inhomogeneous and nonstationary expression. Here, we developed a genetic reporter mouse, Ai38, which expresses GCaMP3 in a Cre-dependent manner from the ROSA26 locus, driven by a strong CAG promoter. Crossing Ai38 with appropriate Cre mice produced robust GCaMP3 expression in defined cell populations in the retina, cortex, and cerebellum. In the primary visual cortex, visually evoked GCaMP3 signals showed normal orientation and direction selectivity. GCaMP3 signals were rapid, compared with virally expressed GCaMP3 and synthetic calcium indicators. In the retina, Ai38 allowed imaging spontaneous calcium waves in starburst amacrine cells during development, and light-evoked responses in ganglion cells in adult tissue. Our results show that the Ai38 reporter mouse provides a flexible method for targeted expression of GCaMP3.
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              Immunohistochemical analysis of neuron types in the mouse small intestine.

              The definition of the nerve cell types of the myenteric plexus of the mouse small intestine has become important, as more researchers turn to the use of mice with genetic mutations to analyze roles of specific genes and their products in enteric nervous system function and to investigate animal models of disease. We have used a suite of antibodies to define neurons by their shapes, sizes, and neurochemistry in the myenteric plexus. Anti-Hu antibodies were used to reveal all nerve cells, and the major subpopulations were defined in relation to the Hu-positive neurons. Morphological Type II neurons, revealed by anti-neurofilament and anti-calcitonin gene-related peptide antibodies, represented 26% of neurons. The axons of the Type II neurons projected through the circular muscle and submucosa to the mucosa. The cell bodies were immunoreactive for choline acetyltransferase (ChAT), and their terminals were immunoreactive for vesicular acetylcholine transporter (VAChT). Nitric oxide synthase (NOS) occurred in 29% of nerve cells. Most were also immunoreactive for vasoactive intestinal peptide, but they were not tachykinin (TK)-immunoreactive, and only 10% were ChAT-immunoreactive. Numerous NOS terminals occurred in the circular muscle. We deduced that 90% of NOS neurons were inhibitory motor neurons to the muscle (26% of all neurons) and 10% (3% of all neurons) were interneurons. Calretinin immunoreactivity was found in a high proportion of neurons (52%). Many of these had TK immunoreactivity. Small calretinin neurons were identified as excitatory neurons to the longitudinal muscle (about 20% of neurons, with ChAT/calretinin/+/- TK chemical coding). Excitatory neurons to the circular muscle (about 10% of neurons) had the same coding. Calretinin immunoreactivity also occurred in a proportion of Type II neurons. Thus, over 90% of neurons in the myenteric plexus of the mouse small intestine can be currently identified by their neurochemistry and shape.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                12 February 2019
                2019
                : 8
                : e42914
                Affiliations
                [1 ]deptLaboratory for Enteric NeuroScience (LENS), Translational Research Center for Gastrointestinal Disorders (TARGID) University of Leuven LeuvenBelgium
                [2 ]deptDepartment of Anatomy and Neuroscience University of Melbourne MelbourneAustralia
                [3 ]deptLaboratory for Neurobiology and Gene Therapy, Department of Neurosciences KU Leuven LeuvenBelgium
                [4 ]deptLeuven Viral Vector Core KU Leuven LeuvenBelgium
                [5 ]deptDepartment of Pathology, GROW-School for Oncology and Developmental Biology Maastricht University Medical Center MaastrichtThe Netherlands
                [6 ]deptBiomedical Research Institute (BIOMED) Hasselt University HasseltBelgium
                Harvard Medical School United States
                Brandeis University United States
                Harvard Medical School United States
                United States
                Author information
                http://orcid.org/0000-0002-3888-971X
                http://orcid.org/0000-0002-9701-8252
                http://orcid.org/0000-0001-8966-2921
                http://orcid.org/0000-0002-2426-0451
                http://orcid.org/0000-0002-0009-2094
                Article
                42914
                10.7554/eLife.42914
                6391068
                30747710
                01364aeb-bb9c-4a75-9507-6a6a58ec9e2c
                © 2019, Li et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 17 October 2018
                : 11 February 2019
                Funding
                Funded by: Chinese Scholarship Council;
                Award ID: 201408370078
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000925, National Health and Medical Research Council;
                Award ID: APP1655567
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100003130, Fonds Wetenschappelijk Onderzoek;
                Award ID: 12G1214N
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004040, KU Leuven;
                Award ID: C32/15/031
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100003130, Fonds Wetenschappelijk Onderzoek;
                Award ID: SBO/S006617N
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100003130, Fonds Wetenschappelijk Onderzoek;
                Award ID: G.0921.15
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100012220, Hercules Foundation;
                Award ID: AKUL/15/37
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100012220, Hercules Foundation;
                Award ID: AKUL/11/37
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100012220, Hercules Foundation;
                Award ID: AKUL/13/37
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002661, Belgian National Fund for Scientific Research;
                Award ID: G.0921.15 SBO/S006617N
                Award Recipient :
                Funded by: Instituut voor Innovatie door Wetenschap en Technologie;
                Award ID: SBO/130065
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Neuroscience
                Custom metadata
                Calcium response profiling of large populations of enteric neurons reveals hard-wired neural circuits that reflect the motility program portfolio of the intestinal region they occupy.

                Life sciences
                calcium imaging,enteric nervous system,neurocircuitry,motility,neural tracing,intestine,mouse

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