FP7Индивидуална стипендия2008–2010

CELL SHAPE, FLY · Control of cell shape in the peripodial membrane of the wing disc of Drosophila melanogaster

7РП — „Хора“ (Действия „Мария Кюри“)

Период
2008-06-01 → 2010-12-31
Финансиране от ЕС
169 391 €
Участници
1
Схема
MC-IEF

Линиите свързват координатора с партньорите.

Накратко на български

Механизмите за промяна на формата на клетките при формирането на крилото на плодовата муха се анализират чрез наблюдение извън организма. Това помага да се разбере как силите в тъканите превръщат простата клетъчна структура в сложен орган по време на метаморфозата.

Този кратък обзор е генериран от изкуствен интелект

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

Резултати накратко

Control of cell shape in the peripodial membrane of the wing disc of Drosophila melanogaster

Drosophila has been broadly used as a model system for studying development. Their short life cycle and genetic tools has made the fly, an ideal model to approach the complexity of the morphogenetic events. In the last decade, the possibility of imaging the live development of the embryo, using reported green fluorescent protein (GFP)-tagged proteins has allow a deeply understanding of the morphogenetic movements. However, little was known about the development movements involved in the metamorphosis. Metamorphosis is major event in Drosophila life cycle; there is a massive rearrangement of tissues responsible of generating from the larval tissues the adult fly. The high dynamicity of the process and the fact that the tissues involved are buried inside of the larva, has made difficult an approach to study in detail this processes. Experiments in the 1970s describe the composition of the media necessary to produce ex vivo the metamorphosis. The hormone responsible of inducing the process is the ecdysone, also known as moulting hormone. We have reproduced these experiments, focusing in the development of the wing, .We have develop a system that allows us to produce ex vivo the metamorphosis of the wing, dissecting the tissue that will develop the wing, known as wing disc, we are able to film its development using confocal technology. This has allow us to describe in cellular detail the complex movements responsible of folding a relatively simple double epithelium sac, the wing discs into a more complex structure, a wing. We analysed what and where are the forces generated in this epithelium sac, responsible of sculpting the tissue; and what is the cellular response of different epithelial cells once their are stretched by this forces. The high conservation between flies and mammal make us confident that the movements described have a homology with mammal development. This ex-vivo model system will allow further studies of other developmental processes such programmed cell death. The culture technique is versatile and could be extended to other tissues, and will allow live imaging of different processes giving a deeper understanding of them.

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

Цел на проекта

I propose to analyze how epithelial cell shape is controlled, using the Drosophila peripodial membrane as a model system. Drosophila third instar imaginal discs are a composed of two contiguous layers of cells of distinct morphology: a pseudostratified one, called the proper epithelium (PE), and a squamous epithelium, the peripodial membrane (PM). While the PE has been deeply studied, little is known about the PM. The peripodial membrane has the ability to change its shape in response to ecdysone; it is proposed that this change is responsible for the eversion of the disc during metamorphosis. I propose to study the control of cell shape in the PM by two perspectives. First, I will look for the factors involved in specifying and maintaining the shape of the PM cells. Second, I will examine the dynamic process of disc eversion, and analyse what shape changes the cells undergo, and what factors and cellular rearrangements are responsible for this fundamental morphological process. For this purpose I have developed a technique that allows me to watch dissected live discs, and to follow the eversion in vitro using confocal live imaging. Amongst other mechanisms, I am currently analysing the role of myosin II in this process as well as looking for new factors that may be involved.

Оригинален текст от CORDIS (на английски).

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Данни: CORDIS, © Европейски съюз