Evidence map›Paper›PMID 31533018›Full record

ArticleJournal of neurophysiology2019

Increasing the expression level of ChR2 enhances the optogenetic excitability of cochlear neurons.

Xiankai Meng, Swetha Murali, Yen-Fu Cheng, Jingrong Lu, Ariel E Hight, Vivek V Kanumuri, M Christian Brown, Jeffrey R Holt, Daniel J Lee, Albert S B Edge

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Overexpression of enhanced yellow fluorescent protein fused with Channelrhodopsin-2 causes contractile dysfunction in skeletal muscle.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  3. Article
  4. Auditory hair cells and spiral ganglion neurons regenerate synapses with refined release properties in vitro.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Functional Connectome Analysis of the Striatum with Optogenetics.Advances in experimental medicine and biology · 2021
    Article
  9. Optical stimulation of neural tissue.Healthcare technology letters · 2020
    Article
  10. Frequency-Specific Optogenetic Deep Brain Stimulation of Subthalamic Nucleus Improves Parkinsonian Motor Behaviors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Xiankai MengEaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts.ORCID 0000-0001-8936-887X
Swetha MuraliDepartment of Otolaryngology, F.M. Kirby Neurobiology Center, Boston Children's Hospital/Harvard Medical School, Boston, Massachusetts.
Yen-Fu ChengEaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts.
Jingrong LuEaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts.
Ariel E HightEaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts.
Vivek V KanumuriEaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts.
M Christian BrownEaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts.
Jeffrey R HoltDepartment of Otolaryngology, Harvard Medical School, Boston, Massachusetts.
Daniel J LeeEaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts.
Albert S B EdgeEaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, Massachusetts.

Funding

Cellular therapy for the inner earR01DC007174 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI EDGE, ALBERT · 2005 to 2017
$4.6M
Delivery of Channel Rhodopsin for Optogenetic Control of Neurons in the CochleaR21DC012422 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI LEE, DANIEL J. · 2012 to 2013
$436k
NIDCD NIH HHS R01 DC007174NIDCD NIH HHS R21 DC012422
6 · The paper itself

Abstract

Optogenetics comprise a promising alternative to electrical stimulation for characterization of neural circuits and for the next generation of neural prostheses. Optogenetic stimulation relies on expression of photosensitive microbial proteins in animal cells to initiate a flow of ions into the cells in response to visible light. Here, we generated a novel transgenic mouse model in which we studied the optogenetic activation of spiral ganglion neurons, the primary afferent neurons of the auditory system, and showed a strong optogenetic response, with a similar amplitude as the acoustically evoked response. A twofold increase in the level of channelrhodopsin expression significantly increased the photosensitivity at both the single cell and organismal levels but also partially compromised the native electrophysiological properties of the neurons. The importance of channelrhodopsin expression level to optogenetic stimulation, revealed by these quantitative measurements, will be significant for the characterization of neural circuitry and for the use of optogenetics in neural prostheses.

Indexed as

Electrophysiological PhenomenaOptogeneticsAnimalsChannelrhodopsinsCochleaEvoked Potentials, Auditory, Brain StemMiceMice, TransgenicModels, AnimalNeurons, AfferentSpiral GanglionChannelrhodopsinsauditory brainstem responseChR2 expression leveloptogenetic stimulationspiral ganglion neuron

Identifiers

PMID31533018
PMCPMC6879948

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.