FP6Реинтеграция2005–2007

NEURONAL DEATH IN PD · Molecular mechanisms of neurodegeneration: targeting programmed cell death as a new therapeutic strategy for Parkinson's disease

6РП — Действия „Мария Кюри“

Период
2005-12-01 → 2007-11-30
Финансиране от ЕС
80 000 €
Участници
2
Схема
IRG

Линиите свързват координатора с партньорите. За проекти отпреди 2014 г. CORDIS не винаги дава точни координати. Тези точки са на ниво град или държава.

Накратко на български

Молекулярните механизми, които активират протеина Bax и водят до програмирана смърт на допаминовите неврони, се анализират чрез модел с токсина MPTP. Разбирането на тези процеси помага за разработването на нови терапевтични стратегии при болестта на Паркинсон.

Този кратък обзор е генериран от изкуствен интелект

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

Цел на проекта

This proposal is designed to pursue our studies of the pathogenesis of Parkinson's disease (PD). Pertinent to this goal, it has been found that 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), a toxin that kills dopaminergic (DA) neurons of the substan tia nigra pars compacta as seen in PD, can execute these neurons by the molecularly regulated form of cell death termed programmed cell death (PCD).However, at present there are no molecular tools of potential therapeutic significance to interfere with this process. In keeping with this, we have previously demonstrated that activation of Bax, a potent pro-cell death protein, governs the PCD of DA neurons in this PD model, and it has been shown that Bax is also activated in PD human brain tissues. However, it is not known what controls the conversion of Bax from the inactive to the active conformation. Recent evidence indicates that activation of Bax requires interaction with the small BH3-only proteins of the Bcl-2 family.Accordingly, Specific Aim I (SA-I) will define the role of BH3-only molecules Puma and Noxa in MPTP-related Bax activation and DA neurodegeneration and its dependency on the transcription factor p53. SA-II will determine the occurrence of a transcription-independent role for p53 at the level of the mitochondria on MPTP-related Bax activation and DA neurodegeneration. SA-III will determine the role of BH3-only molecule Bim in MPTP-induced Bax activation and DA neurodegeneration and its dependency on the c-Jun N-terminal kinase (JNK) pathway.Finally, SA-IV will assess the effect of two new molecules that interfere with Bax activation as potential therapeutic tools for PD-related DA neurodegeneration. Overall, this proposal should (i) lay the ground for the development of novel therapeutic strategies for PD and (ii) allow my professional integration to European research by providing substantial funding to develop my own research group in Spain.

Оригинален текст от CORDIS (на английски).

Участници

  • INSTITUT DE RECERCA HOSPITAL UNIVERSITARI VALL D'HEBRON · BARCELONAКоординаторИспания
  • INSTITUT D'INVESTIGACIONS BIOMEDIQUES AUGUST PI-SUNYER' · BARCELONAНиво градИспания

Връзки

Данни: CORDIS, © Европейски съюз