H2020Индивидуална стипендия2018–2020

LEVADAPT · Identification of new regulators of Acetylcholine receptor using the nematode Caenorhabditis elegans

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период
2018-05-01 → 2020-05-11
Финансиране от ЕС
185 076 €
Участници
1
Схема
MSCA-IF

Линиите свързват координатора с партньорите.

Накратко на български

Регулаторите на ацетилхолиновите рецептори се проучват чрез наблюдение на червеи C. elegans и тяхната реакция към веществото левамизол. Това помага за разбирането на механизмите при невродегенеративни заболявания като Алцхаймер и Паркинсон, както и при мускулни болести като миастения гравис.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Identification of new regulators of Acetylcholine receptor using the nematode Caenorhabditis elegans

Nicotinic acetylcholine receptors (nAChRs) are pentameric ligand-gated ion channels that have been highly conserved throughout evolution and play key roles in numerous physiological and pathological processes in humans. In the central nervous system, nAChRs have important roles in diverse processes including learning, memory and attention. Alterations of nAChR-related signalling contribute to neurodegenerative disorders such as Alzheimer’s or Parkinson’s disease. In the peripheral nervous system, nAChRs are responsible for the fast-excitatory neurotransmission at neuromuscular junctions. At the neuromuscular junction, AChRs are localized at the surface of the muscles where they are activated by the release of acetylcholine from motoneuron. Activation of AChRs eventually trigger muscle contraction and then malfunction of AChRs lead to severe neuromuscular diseases such as myasthenia gravis or congenital myasthenic syndrome. The free-living nematode worm Caenorhabditis elegans is a powerful model organism to study neuromuscular system and AChR function. In C. elegans, as in mammals, acetylcholine is the neurotransmitter used to trigger muscle contraction. A subclass of AChR present at the neuromuscluar junction has been well studied due to its sensitivity to levamisole, a nematode-specific agonist . Prolonged exposure to levamisole causes hyperactivation of AChR and then hypercontraction of C. elegans muscles leading to paralysis and eventually death of worms. However, mutations in genes regulating AChR biosynthesis, activity or clustering modify the response of the worms to levamisole. As wild-type worms, the mutant worms initially paralysed when exposed to levamisole but after several hours they remain hypercontracted and start to move again. At the molecular level, this hypercontraction of adapting worms is characterized by a sustained elevated level of calcium in the muscle which is not observed in wild-type animals. This project aimed to characterize the mechanisms that allow adapting worms to overcome the stress induced by sustained hypercontraction of muscle cells and to recover locomotion in a such situation. More generally, the goal is to study the mechanisms underlying the adaptation of striated muscle cells to the stress triggered by muscle hyperactivity.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Acetylcholine receptor is an essential component of central and peripheral nervous systems which plays a key role in numerous physiological and pathological processes. In particular, acetylcholine receptor is responsible for the coupling between nervous and muscular system at the neuromuscular junction as they are activated following acetylcholine release from neurons to triggers muscle contraction. Despite extensive work to decipher the molecular properties of the receptor itself, how the activity of the receptor and the signal following its activation are modulated is still poorly understood. This is yet an important question to address as impairment in acetylcholine receptor-associated signalling is involved in neuromuscular pathologies such as myasthenia gravis or congenital myasthenic syndrome. Here, we propose to use the genetic animal model Caenorhabditis elegans to study the dynamic regulation of acetylcholine receptors. This nematode is a powerful tool to study acetylcholine receptor as this animal also uses acetylcholine as an excitatory neurotransmitter at the neuromuscular junction. In nematode, acetylcholine receptors are sensitive to levamisole, a specific agonist. Prolonged exposure to levamisole leads to hypercontraction of the worms and finally to their paralysis. However, mutations in genes associated to acetylcholine receptor activity or biosynthesis enable the worms to adapt to levamisole. In this project, using proteomic and genetic approaches based on levamisole adaptation, we will identify several new regulators of acetylcholine receptor and of the associated signalling pathway. Deeper functional characterization will be performed on the new regulators evolutionary conserved that then may be involved in some neuromuscular pathologies. This research will give new insights into functional dynamic of acetylcholine receptor and may then shed a new light on the cause of impaired functioning of acetylcholine receptor in diseases.

Оригинален текст от CORDIS (на английски).

Участници

  • UNIVERSITE LYON 1 CLAUDE BERNARD · Villeurbanne CedexКоординаторФранция

Връзки

Данни: CORDIS, © Европейски съюз