SYNAPSE FORMATION · The role of filopodia in synapse formation in absence of dendritic spines
6РП — Действия „Мария Кюри“
- Период
- 2007-05-01 → 2009-04-30
- Финансиране от ЕС
- 148 588 €
- Участници
- 1
- Схема
- EIF
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
Синапсите, чрез които невроните комуникират, се формират по различен начин в зависимост от това дали пренасят възбуждащи или инхибиращи сигнали (като GABA). Разбирането на тези процеси помага да се разбере как мозъкът се адаптира към околната среда и функционира стабилно.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Final Activity Report Summary - SYNAPSE FORMATION (The role of filopodia in synapse formation in absence of dendritic spines)
Chemical synapses are the key connective elements in neuronal networks. They are not only crucial for information processing but their plasticity also endows the brain with its outstanding capacity for adaptation to the environment. Understanding synapses, and how they are formed, is therefore a fundamentally important task in neuroscience. So far, most studies have focused on the formation of glutamatergic synapses while the formation of the other major type of synapses in the brain, which use the inhibitory transmitter GABA, remains less examined, in spite of the fact that GABAergic synapses form 10-20 % of all synapses in the brain and are indispensable for proper and stable functioning of in the brain. Glutamatergic synapses on excitatory neurons in the hippocampus are almost exclusively located on dendritic spines. It has been shown that dendrites play an active role in the formation of new glutamatergic synapses by growing out small protrusions which make contact with presynaptic axons and boutons. In contrast to glutamatergic synapses, GABAergic synapses are usually not located on spines, but directly on the dendritic shaft. We used high-resolution two-photon imaging to examine the formation of GABAergic synapses in the CA1 area of organotypical hippocampal cultures. We made use of GAD65-GFP mice, in which a subset of GABAergic interneurons expresses GFP. CA1 pyramidal neurons were filled with Alexa Fluor 594 through a patch pipette. We found that GABAergic synapses are formed via a fundamentally different process than glutamatergic spine synapses. Outgrowing dendritic protrusions can distinguish between potential presynaptic partners. Whereas contacts with glutamatergic boutons could be long-lasting, contacts with GABAergic boutons were always short-lived and resulted in retraction of the dendritic protrusions. Similarly, contacts made by GABAergic axonal protrusions were always transient. This strongly suggests that axonal and dendritic protrusions do not mediate the formation of GABAergic synapses. New GABAergic contacts were formed exclusively at locations where GABAergic axons and postsynaptic dendrite are already in close proximity: by the appearance of new boutons at preexisting axon-dendrite crossings. These findings imply that GABAergic axons in a mature network can make new synapses only with postsynaptic partners that are in their immediate neighborhood, which is in marked contrast to the way glutamatergic synapses are made. This puts significant structural constraints on the generation and plasticity of GABAergic and glutamatergic synapses which will be important to be kept in mind when trying to understand development and plasticity of the intricate neural networks of the brain.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
One of the fundamental questions in neurobiology is how synapses are formed. Dendritic filopodia are thought to play an important role in the generation of excitatory synapses on dendritic spines.They find and make initial contact with an appropriate axon and then retract to the dendrite and become spines. Much less is known about the role of filopodia - if any - in the generation of synapses on the dendritic shaft.The aim of the proposed project is to elucidate this process by following the formation of shaft synapses using two-photon laser scanning microscopy. Most studies on synapse formation have concentrated on excitatory synapses, but I will examine inhibitory synapses, which never occur on spines.Postsynaptic dendrites of pyramidal cells and GABAergic axons will be visualized with different fluorescent labels in hippocampal slice cultures by filling individual neurons and/or by using transgenic mice that express Green Fluorescent Protein (GFP) in a specific subset of neurons.I will follow the morphological changes of the axon and dendrite at locations where they make contact. The formation of functional synapses will be verified by FM1-43 labelling, which marks presynaptic terminals that recycle vesicles. Once the initial events in GABAergic synapse formation under control conditions have been established, I will assess the regulation of these events by factors that are known to have an effect on GABAergic synapse formation.Such factors could be pharmacological agents such as TTX, bicuculline and BDN F, or postsynaptic Cl- concentration. The results of the proposed experiments will lead to a better understanding of the initial steps in GABAergic synapse formation and factors influencing this process.This will contribute to the understanding how neuron al networks are formed during development and how they can continue to remodel during learning and adaptation.
Оригинален текст от CORDIS (на английски).
Участници
- MAX PLANCK INSTITUTE FOR NEUROBIOLOGY · MARTINSRIEDКоординаторНиво градГермания
Връзки
Данни: CORDIS, © Европейски съюз
