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A Systems Level Analysis of Neuronal Network Function in the Olfactory Bulb: Coding, Connectivity, and Modular organization

dc.contributor.advisorSchild, Detlev Prof. Dr. Dr.de
dc.contributor.authorChen, Tsai-Wende
dc.date.accessioned2013-01-22T15:47:52Zde
dc.date.available2013-01-30T23:50:59Zde
dc.date.issued2008-12-15de
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-000D-F166-0de
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-3468
dc.format.mimetypeapplication/pdfde
dc.language.isoengde
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/de
dc.titleA Systems Level Analysis of Neuronal Network Function in the Olfactory Bulb: Coding, Connectivity, and Modular organizationde
dc.typedoctoralThesisde
dc.title.translatedA Systems Level Analysis of Neuronal Network Function in the Olfactory Bulb: Coding, Connectivity, and Modular organizationde
dc.contributor.refereeWolf, Fred Prof. Dr.de
dc.date.examination2008-05-08de
dc.subject.dnb570 Biowissenschaften, Biologiede
dc.subject.gokWCK 000de
dc.subject.gokWA 310de
dc.subject.gokMED 311de
dc.description.abstractengThe olfactory bulb (OB) is the first brain region that receives and processes sensory inputs from the nose. It contains highly specialized neuronal networks organized by individual glomeruli, which are sites of synaptic contacts between olfactory sensory neurons (OSN) and secondary mitral/tufted (M/T) cells in the OB. In this thesis, I explored the neuronal network function of a vertebrate OB system, using a combination of calcium imaging and electrophysiological techniques. In the first part of the thesis, I introduced a number of image processing techniques for analyzing functional calcium imaging data. This facilitates the selection of regions of interest and allows visualizing fine processes of neurons in densely stained brain tissues. In the second part of the thesis, we explored the dynamics of [Ca2+] activity of M/T cell population. This led to the identification of distinct subpopulations of neurons that showed highly synchronous spontaneous [Ca2+] activity. Anatomical reconstruction revealed that these synchronous neurons were invariably connected to the same glomerulus. Furthermore, the odor-induced responses of synchronous neurons were virtually identical, irrespective of whether the responses were excitatory or inhibitory, and irrespective of the distance between them. In the third part of the thesis, we analyzed the mechanism underlying the synchronous responses. We show that synchronous neurons received correlated EPSC inputs and were coupled by gap junctions. Together, these data reveal that odors are represented in the OB by modules of distributed and synchronous M/T cells associated with the same glomeruli. This may allow for parallel input to higher brain centers.de
dc.contributor.coRefereeStühmer, Walter Prof. Dr.de
dc.subject.topicMolecular Biology & Neurosciences Programde
dc.subject.gerCalcium imagingde
dc.subject.gerOlfactory bulbde
dc.subject.gerMitral Cellde
dc.subject.gerSynchronous activityde
dc.subject.gerGlomerulusde
dc.subject.gerNeuronal Networkde
dc.subject.gerImage Processingde
dc.subject.engCalcium imagingde
dc.subject.engOlfactory bulbde
dc.subject.engMitral Cellde
dc.subject.engSynchronous activityde
dc.subject.engGlomerulusde
dc.subject.engNeuronal Networkde
dc.subject.engImage Processingde
dc.subject.bk42.17de
dc.subject.bk42.12de
dc.identifier.urnurn:nbn:de:gbv:7-webdoc-1794-3de
dc.identifier.purlwebdoc-1794de
dc.identifier.ppn596076037de


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