FP7Индивидуална стипендия2009–2011

MICE SPINAL CORD CM · Neuronal circuitry and plasticity of the spinal cord using in-vivo electrophysiology in transgenic mice

7РП — „Хора“ (Действия „Мария Кюри“)

Период
2009-12-01 → 2011-11-30
Финансиране от ЕС
203 818 €
Участници
1
Схема
MC-IEF

Линиите свързват координатора с партньорите.

Накратко на български

Невронните връзки в гръбначния стълб на мишки се анализират чрез измерване на електрическата активност на двигателните неврони. Това помага за разбирането на нормалните функции на гръбнака и причините за тяхното нарушаване при заболявания като амиотрофична латерална склероза (ALS).

Този кратък обзор е генериран от изкуствен интелект

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

Резултати накратко

Neuronal circuitry and plasticity of the spinal cord using in-vivo electrophysiology in transgenic mice

Project context and objectives The project had the following aims: - to develop the techniques for intracellular recordings of spinal neurones previously used in larger animals (e.g. a cat) for the adult mouse in vivo; - to describe the intrinsic properties of mouse motoneurones and to compare those properties with those described in the cat and the rat; - to investigate differences in various transgenic strains. Work performed Larger animals have traditionally been used for in vivo intracellular recording in the adult spinal cord due to the stability needed for intracellular penetrations with fine electrodes and the robustness of the preparation to withstand the surgical procedures. To be able to take advantage of the developments in transgenic mice so as to understand both normal spinal function and its dysfunction in disease, it is necessary to adapt previous techniques used in the larger animals and transfer them to the mouse. Main results We successfully developed a laboratory capable of intracellular recording from identified spinal motoneurones in the adult mouse in vivo. Using these adapted techniques, we identified key intrinsic properties of the motoneurones. We then extended the model to include a decerebrate preparation and compared these results with those obtained using different anaesthesias. Using the decerebrate in vivo model we also demonstrated that is it possible to pharmacologically activate spinal 'central pattern generators', such as locomotion, simultaneously with intracellular recording. By applying the model to transgenic models of human disorders, we explored the hypothesis of an increased level of excitability in a transgenic mouse model of the human motoneurone disease, Amyotrophic Lateral Sclerosis (ALS), demonstrating that the increased excitability seen in the neonatal in vitro preparations extends into adulthood. These results have been disseminated in the form of published manuscripts in peer reviewed journals (three so far) and in abstract form at various international meetings. The work has also been covered by Insight Publishers / Projects 27, pp 54-56 in an article named 'Mice models build a bridge' (see www.projectsmagazine.eu.com for more detail). This grant has allowed us to establish a laboratory here in Europe, which is currently one of a handful worldwide that are capable of conducting such experiments in the adult mouse spinal cord in vivo. This has culminated in a number of potentially high profile international collaborations. In the coming years we will use the in-vivo model to study transgenic mice with specific manipulations that affect the development of spinal neuronal circuitry and those that have genetic mutations similar to those underlying neurological disorders in humans. Project website: http://www.cph-ncm.ku.dk/about/transgenicmice

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

Цел на проекта

The development of transgenic mice affecting development of spinal cord circuitry or mimicking hereditary neurological motor disorders has necessitated the development of in-vivo adult mouse preparations for electrophysiology to bridge molecular biology with the pathophysiology of phenotypes. The first goal is the development and refinement of a “mouse in-vivo spinal cord preparation” for intracellular recordings and analysis of spinal circuitry in “acute experiments” and a preparation for chronic recording of EMG and kinematics. These will be used to identify specific patterns of inputs to motoneurones in the mouse including the Ia monosynaptic EPSP, presynaptic inhibition, reciprocal inhibition, recurrent inhibition, propioceptive and exteroceptive polysynaptic inputs as well as the intrinsic properties of motoneurones. The data will not only characterise synaptic connectively in the mouse which can be compared to other species but will serve as control data for the rest of the project. The second goal is the use of the preparations to study transgenic mice with specific manipulations affecting the development of spinal neuronal circuitry. 2 mice mutants developed by Thomas Jessell (New York) and Silvia Arber (Basel) will be used. In the Er81 mutant mouse lack of a transcription factor causes Ia propioceptive afferents to terminate prematurely in the intermediate spinal cord. The second mutant model lacks the presynaptic GABAergic terminals on Ia afferent inputs to motoneurones. The researcher will investigate the plasticity occurring as a consequence. The third goal is to use the preparations to study transgenic mice with genetic mutations similar to those underlying neurological disorders in humans. For this the researcher will investigate plasticity in mice with a mutation affecting the glycine receptor, mimicking hyperekplexia in humans. SOD-1 mutants, models of ALS will also be used to investigate excitability changes at central part of motoneurone

Оригинален текст от CORDIS (на английски).

Участници

  • KOBENHAVNS UNIVERSITET · KOBENHAVNКоординаторДания

Връзки

Данни: CORDIS, © Европейски съюз