Evidence map›Paper›PMID 31362954›Full record

ArticleeNeuro

Blue Light Promotes Neurite Outgrowth of Retinal Explants in Postnatal ChR2 Mice.

Chin-I Lin, Chuan-Chin Chiao

Abstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

2 authors.

Chin-I LinInstitute of Systems Neuroscience, National Tsing Hua University, Hsinchu 30013, Taiwan.ORCID 0000-0002-9170-4403
Chuan-Chin ChiaoInstitute of Systems Neuroscience, National Tsing Hua University, Hsinchu 30013, Taiwan ccchiao@life.nthu.edu.tw.ORCID 0000-0001-9506-0230

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurons in the adult mammalian CNS fails to regenerate after severe injury. However, it is known that an increase in neural activity occurs in mouse retinal ganglion cells (RGCs) after extrinsic stimulation and this can induce axon growth. In the present study, we applied an optogenetic approach using a mouse model, specifically involving channelrhodopsin-2 (ChR2) expression in RGCs. We investigated whether modulation of RGC neural activity exclusively by blue light stimulation is able to promote neurite outgrowth of postnatal retinal explants. The results showed that activation of RGCs expressing ChR2 by 20 Hz blue light for 1 h is a most effective way of enhancing neurite outgrowth in postnatal retinas. This is achieved via gap junctions that spread neural activity across the whole retina. Moreover, we found that activation of intrinsic photosensitive RGCs (ipRGCs) by blue light also contributes significantly to the promotion of neurite outgrowth in the same postnatal retinal explants. Our findings not only demonstrate that a short-term increase in RGC neural activity is sufficient to facilitate the neurite outgrowth of retinal explants, but also highlight the fact that the temporal pattern of neural activity in RGCs is a critical factor in regulating axon regeneration.

Indexed as

AnimalsCells, CulturedChannelrhodopsinsFemaleLightMaleMice, Inbred C57BLMice, TransgenicNeuritesOptogeneticsPhotic StimulationRetinal Ganglion CellsChannelrhodopsinsaxon regenerationchannelrhodopsin-2intrinsic photosensitive retinal ganglion cellslight stimulationretinal ganglion cells

Identifiers

PMID31362954
PMCPMC6712202

What OpenQuestion holds

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LicenceCC BY
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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.