Minimally invasive multimode optical fiber microendoscope for deep brain fluorescence imaging

A major open challenge in neuroscience is the ability to measure and perturb neural activity in vivo from well defined neural sub-populations at cellular resolution anywhere in the brain. However, limitations posed by scattering and absorption prohibit non-invasive multi-photon approaches for deep (...

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Bibliographic Details
Main Authors: Ohayon, Shay (Author), DiCarlo, James (Author)
Other Authors: McGovern Institute for Brain Research at MIT (Contributor), Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences (Contributor)
Format: Article
Language:English
Published: The Optical Society, 2020-08-20T11:16:55Z.
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Online Access:Get fulltext
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001 126696
042 |a dc 
100 1 0 |a Ohayon, Shay  |e author 
100 1 0 |a McGovern Institute for Brain Research at MIT  |e contributor 
100 1 0 |a Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences  |e contributor 
700 1 0 |a DiCarlo, James  |e author 
245 0 0 |a Minimally invasive multimode optical fiber microendoscope for deep brain fluorescence imaging 
260 |b The Optical Society,   |c 2020-08-20T11:16:55Z. 
856 |z Get fulltext  |u https://hdl.handle.net/1721.1/126696 
520 |a A major open challenge in neuroscience is the ability to measure and perturb neural activity in vivo from well defined neural sub-populations at cellular resolution anywhere in the brain. However, limitations posed by scattering and absorption prohibit non-invasive multi-photon approaches for deep (>2mm) structures, while gradient refractive index (GRIN) endoscopes are relatively thick and can cause significant damage upon insertion. Here, we present a novel micro-endoscope design to image neural activity at arbitrary depths via an ultra-thin multi-mode optical fiber (MMF) probe that has 5-10X thinner diameter than commercially available microendoscopes. We demonstrate micron-scale resolution, multi-spectral and volumetric imaging. In contrast to previous approaches, we show that this method has an improved acquisition speed that is sufficient to capture rapid neuronal dynamics in-vivo in rodents expressing a genetically encoded calcium indicator (GCaMP). Our results emphasize the potential of this technology in neuroscience applications and open up possibilities for cellular resolution imaging in previously unreachable brain regions. 
520 |a National Institutes of Health (U.S.) (Grant (REY026436A) 
546 |a en 
655 7 |a Article 
773 |t 10.1364/BOE.9.001492 
773 |t Biomedical optics express