Literature DB >> 23792946

SeeDB: a simple and morphology-preserving optical clearing agent for neuronal circuit reconstruction.

Meng-Tsen Ke1, Satoshi Fujimoto, Takeshi Imai.   

Abstract

We report a water-based optical clearing agent, SeeDB, which clears fixed brain samples in a few days without quenching many types of fluorescent dyes, including fluorescent proteins and lipophilic neuronal tracers. Our method maintained a constant sample volume during the clearing procedure, an important factor for keeping cellular morphology intact, and facilitated the quantitative reconstruction of neuronal circuits. Combined with two-photon microscopy and an optimized objective lens, we were able to image the mouse brain from the dorsal to the ventral side. We used SeeDB to describe the near-complete wiring diagram of sister mitral cells associated with a common glomerulus in the mouse olfactory bulb. We found the diversity of dendrite wiring patterns among sister mitral cells, and our results provide an anatomical basis for non-redundant odor coding by these neurons. Our simple and efficient method is useful for imaging intact morphological architecture at large scales in both the adult and developing brains.

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Year:  2013        PMID: 23792946     DOI: 10.1038/nn.3447

Source DB:  PubMed          Journal:  Nat Neurosci        ISSN: 1097-6256            Impact factor:   24.884


  47 in total

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Journal:  Nat Methods       Date:  2007-03-25       Impact factor: 28.547

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6.  Non-redundant odor coding by sister mitral cells revealed by light addressable glomeruli in the mouse.

Authors:  Ashesh K Dhawale; Akari Hagiwara; Upinder S Bhalla; Venkatesh N Murthy; Dinu F Albeanu
Journal:  Nat Neurosci       Date:  2010-10-17       Impact factor: 24.884

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Review 6.  Viral vector-based tools advance knowledge of basal ganglia anatomy and physiology.

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Review 8.  Extracting structural and functional features of widely distributed biological circuits with single cell resolution via tissue clearing and delivery vectors.

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10.  Neural crest defects in ephrin-B2 mutant mice are non-autonomous and originate from defects in the vasculature.

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