Literature DB >> 18925632

Differential expression of canonical (classical) transient receptor potential channels in guinea pig enteric nervous system.

Sumei Liu1, Mei-Hua Qu, Wei Ren, Hong-Zhen Hu, Na Gao, Guo-Du Wang, Xi-Yu Wang, Guijun Fei, Fei Zuo, Yun Xia, Jackie D Wood.   

Abstract

The canonical transient receptor potential (TRPC) family of ion channels is implicated in many neuronal processes including calcium homeostasis, membrane excitability, synaptic transmission, and axon guidance. TRPC channels are postulated to be important in the functional neurobiology of the enteric nervous system (ENS); nevertheless, details for expression in the ENS are lacking. Reverse transcriptase-polymerase chain reaction, Western blotting, and immunohistochemistry were used to study the expression and localization of TRPC channels. We found mRNA transcripts, protein on Western blots, and immunoreactivity (IR) for TRPC1/3/4/6 expressed in the small intestinal ENS of adult guinea pigs. TRPC1/3/4/6-IR was localized to distinct subpopulations of enteric neurons and was differentially distributed between the myenteric and submucosal divisions of the ENS. TRPC1-IR was widely distributed and localized to neurons with cholinergic, calretinin, and nitrergic neuronal immunochemical codes in the myenteric plexus. It was localized to both cholinergic and noncholinergic secretomotor neurons in the submucosal plexus. TRPC3-IR was found only in the submucosal plexus and was expressed exclusively by neuropeptide Y-IR neurons. TRPC4/6-IR was expressed in only a small population of myenteric neurons, but was abundantly expressed in the submucosal plexus. TRPC4/6-IR was coexpressed with both cholinergic and nitrergic neurochemical codes in the myenteric plexus. In the submucosal plexus, TRPC4/6-IR was expressed exclusively in noncholinergic secretomotor neurons. No TRPC1/3/4/6-IR was found in calbindin-IR neurons. TRPC3/4/6-IR was widely expressed along varicose nerve fibers and colocalized with synaptophysin-IR at putative neurotransmitter release sites. Our results suggest important roles for TRPC channels in ENS physiology and neuronal regulation of gut function.

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Year:  2008        PMID: 18925632      PMCID: PMC2577062          DOI: 10.1002/cne.21874

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  88 in total

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  12 in total

1.  Activation of submucosal 5-HT(3) receptors elicits a somatostatin-dependent inhibition of ion secretion in rat colon.

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Authors:  Peter Holzer
Journal:  Pharmacol Ther       Date:  2011-03-21       Impact factor: 12.310

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Journal:  J Neurosci       Date:  2015-02-04       Impact factor: 6.167

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Journal:  Dig Dis Sci       Date:  2016-07       Impact factor: 3.199

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Authors:  K N Westlund; L P Zhang; F Ma; R Nesemeier; J C Ruiz; E M Ostertag; J S Crawford; K Babinski; M M Marcinkiewicz
Journal:  Neuroscience       Date:  2014-01-03       Impact factor: 3.590

Review 6.  Visceral pain from colon and rectum: the mechanotransduction and biomechanics.

Authors:  Bin Feng; Tiantian Guo
Journal:  J Neural Transm (Vienna)       Date:  2019-10-09       Impact factor: 3.575

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Authors:  Laura A Merriam; Carolyn W Roman; Caitlin N Baran; Beatrice M Girard; Victor May; Rodney L Parsons
Journal:  J Mol Neurosci       Date:  2012-04-14       Impact factor: 3.444

Review 8.  TRP channels in neurogastroenterology: opportunities for therapeutic intervention.

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Journal:  Br J Pharmacol       Date:  2011-01       Impact factor: 8.739

9.  Molecular and functional diversity of GABA-A receptors in the enteric nervous system of the mouse colon.

Authors:  Mohsen Seifi; James F Brown; Jeremy Mills; Pradeep Bhandari; Delia Belelli; Jeremy J Lambert; Uwe Rudolph; Jerome D Swinny
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10.  TRPC1 and TRPC6 channels cooperate with TRPV4 to mediate mechanical hyperalgesia and nociceptor sensitization.

Authors:  Nicole Alessandri-Haber; Olayinka A Dina; Xiaoje Chen; Jon D Levine
Journal:  J Neurosci       Date:  2009-05-13       Impact factor: 6.167

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