Abstract

The enteric nervous system plays a critical role in the regulation of gastrointestinal tract functions and is often referred to as the 'second brain' because it shares many features with the central nervous system. These similarities include among others a large panel of neurotransmitters, a large population of glial cells and a susceptibility to neurodegeneration. This close homology between the central and enteric nervous systems suggests that a disease process affecting the central nervous system could also involve its enteric counterpart. This was already documented in Parkinson's disease, the most common synucleinopathy, in which alpha-synuclein deposits are reported in the enteric nervous system in the vast majority of patients. Tau is another key protein involved in neurodegenerative disorders of the brain. Whether changes in tau also occur in the enteric nervous system during gut or brain disorders has just begun to be explored. The scope of the present article is therefore to review existing studies on the expression and phosphorylation pattern of tau in the enteric nervous system under physiological and pathological conditions and to discuss the possible occurrence of 'enteric tauopathies'.

Highlights

  • Tau was one of the first microtubule-associated proteins (MAPs) to be characterised (Weingarten et al 1975) and cloned (Goedert et al 1989)

  • Western Blot analyses confirmed that the tau banding pattern was markedly different between human brain and gut but we identified 1N3R and 0N4R as being the two main tau isoforms expressed in in both the myenteric and submucosal plexus of human adult colon (Lionnet et al 2018) (Figure 2 and 3)

  • Using primary cultures of rat enteric nervous system (ENS), we have shown that foetal rat enteric neurons express five isoforms of tau, including the three 3R isoforms, in sharp contrast to central nervous system (CNS) neurons cultured for similar periods of time (Lionnet et al 2018)

Read more

Summary

Running title Tau in the ENS

List of abbreviations AD: Alzheimer’s disease CBD: corticobasal degeneration CNS: central nervous system EGC: enteric glial cells ENS: enteric nervous system GI: gastrointestinal MAP: microtubule-associated proteins Nrf: nuclear factor erythroid 2–related factor 2 PSP: progressive supranuclear palsy

Introduction
Legends to figure
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call