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  Transmitted light brightfield mosaic microscopy for three-dimensional tracing of single neuron morphology

Oberlaender, M., Bruno, R. M., Sakmann, B., & Broser, P. J. (2007). Transmitted light brightfield mosaic microscopy for three-dimensional tracing of single neuron morphology. Journal of Biomedical Optics, 12(6):, pp. 1-19. doi:10.1117/1.2815693.

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資料種別: 学術論文
その他のタイトル : Transmitted light brightfield mosaic microscopy for three-dimensional tracing of single neuron morphologyneuron morphology

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JBiomedicalOpt_12_2007_064029.pdf (全文テキスト(全般)), 2MB
 
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JBiomedicalOpt_12_2007_064029.pdf
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https://dx.doi.org/10.1117/1.2815693 (全文テキスト(全般))
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 作成者:
Oberlaender, Marcel1, 著者           
Bruno, Randy M.1, 著者           
Sakmann, Bert1, 著者           
Broser, Philip Julian1, 著者           
所属:
1Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society, ou_1497701              

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キーワード: three-dimensional automatic reconstruction; three-dimensional mosaic microscopy; three-dimensional neuron morphology; large data processing; axonal morphology; axons
 要旨: A fundamental challenge in neuroscience is the determination of the three-dimensional (3D) morphology of neurons in the cortex. Here we describe a semiautomated method to trace single biocytin-filled neurons using a transmitted light brightfield microscope. The method includes 3D tracing of dendritic trees and axonal arbors from image stacks of serial 100-microm-thick tangential brain sections. Key functionalities include mosaic scanning and optical sectioning, high-resolution image restoration, and fast, parallel computing for neuron tracing. The mosaic technique compensates for the limited field of view at high magnification, allowing the acquisition of high-resolution image stacks on a scale of millimeters. The image restoration by deconvolution is based on experimentally verified assumptions about the optical system. Restoration yields a significant improvement of signal-to-noise ratio and resolution of neuronal structures in the image stack. Application of local threshold and thinning filters result in a 3D graph representation of dendrites and axons in a section. The reconstructed branches are then manually edited and aligned. Branches from adjacent sections are spliced, resulting in a complete 3D reconstruction of a neuron. A comparison with 3D reconstructions from manually traced neurons shows that the semiautomated system is a fast and reliable alternative to the manual tracing systems currently available.

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言語: eng - English
 日付: 2007-06-192007-04-022007-07-092007-12-282007-12-28
 出版の状態: 出版
 ページ: 19
 出版情報: -
 目次: -
 査読: 査読あり
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出版物 1

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出版物名: Journal of Biomedical Optics
種別: 学術雑誌
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出版社, 出版地: Bellingham, WA : Published by SPIE--the International Society for Optical Engineering in cooperation with International Biomedical Optics Society
ページ: - 巻号: 12 (6) 通巻号: 064029 開始・終了ページ: 1 - 19 識別子(ISBN, ISSN, DOIなど): ISSN: 1083-3668
CoNE: https://pure.mpg.de/cone/journals/resource/954925607859