FP6Индивидуална стипендия2008–2010

WDVPT · Role of the Wnt/b-catenin pathway in the dorso-ventral organisation of the telencephalon

6РП — Действия „Мария Кюри“

Период
2008-04-01 → 2010-03-31
Финансиране от ЕС
169 365 €
Участници
1
Схема
EIF

Линиите свързват координатора с партньорите.

Накратко на български

Молекулните пътища, които определят развитието на предния мозък и очите при зелената риба, се анализират чрез конкретни протеини като FoxG1 и dkk1. Резултатитете помагат за по-доброто разбиране на невродегенеративното разстройство синдром на Рет при хората.

Този кратък обзор е генериран от изкуствен интелект

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

Резултати накратко

Final Activity and Management Report Summary - WDVPT (Role of the Wnt/b-catenin pathway in the dorso-ventral organisation of the telencephalon.)

To obtain the diversity of cells present in the human brain, different signalling molecules are repeatedly used to regionalise the central nervous system (CNS). In this work we used the zebrafish as an organism model to find which signal pathways are involved in the anterior brain formation and when do they act. We restrict our research to the dorsal-ventral (DV) axis (back to front) and to two specific regions; the telencephalon, the most anterior part of the CNS, and the eye. In both cases we found that a specific molecule coordinates different signalling pathways that are responsible for the DV axis. In the telencephalon FoxG1 is the molecule that regulates the signalling pathways; dorsally the Wnt and ventrally the Hedgehog pathway. Recently FoxG1 was implicated in the Human Rett syndrome, a neurodegenerative disorder; we believe that our study can contribute to a better understanding of this syndrome. The transmission of the visual information from the eye to the brain is dependent of a correct patterning of the eye. Here we discovered that dorsal-ventral patterning of the eye is dependent of dkk1. In this tissue, dkk1 regulates the establishment of Dorsal and ventral by coordinating the activity of several signalling pathways: Wnt, Fgf and BMP. These projects unravelled two different mechanisms used by different tissues to reach the same goal of establish a distinct dorsal and ventral programme.

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

Цел на проекта

The complexity of the forebrain makes it a challenging task to elucidate how this structure forms during embryonic development. We are beginning to understand how a simple ectodermal sheet gives rise to the functional forebrain. Its most intricate structure is the telencephalon-derived cortex.A crucial step in forming the cortex is the establishment of distinct dorso-ventral (DV) cell identities. This process is regulated by Hedgehog (Hh) signalling as its abrogation prevents formation of ventral telencephalon.However, the DV organisation is restored in the absence of both Hh signalling and its repressor Gli3, indicating that another mechanism is able to establish the DV polarity in this context. Here, we propose that this is achieved via the Wnt/b-catenin signalling pathway.We aim to elucidate- the mechanisms by which this pathway regulates the DV telencephalic patterning and- the nature of the interactions existing between Hh and Wnt/b-catenin signalling in this process.

Оригинален текст от CORDIS (на английски).

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Данни: CORDIS, © Европейски съюз