Evidence map›Paper›PMID 31105708›Full record

ArticleFrontiers in immunology2019

Microglia Mediate Synaptic Material Clearance at the Early Stage of Rats With Retinitis Pigmentosa.

Juncai He, Congjian Zhao, Jiaman Dai, Chuan Huang Weng, Bai Shi Jiao Bian, Yu Gong, Lingling Ge, Yajie Fang, Hui Liu, Haiwei Xu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
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

23 citing papers in PubMed, 30 citations in OpenAlex.

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  18. Engulfed by Glia: Glial Pruning in Development, Function, and Injury across Species.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
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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

11 authors at 2 institutions in 1 country.

Juncai HeSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Congjian ZhaoSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Jiaman DaiSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Chuan Huang WengSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Bai Shi Jiao BianSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Yu GongSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Lingling GeSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Yajie FangSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Hui LiuSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Haiwei XuSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Zheng Qin YinSouthwest Hospital/Southwest Eye Hospital, Third Military Medical University (Amy Medical University), Chongqing, China.
Southwest Hospital · CNArmy Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resident microglia are the main immune cells in the retina and play a key role in the pathogenesis of retinitis pigmentosa (RP). Many previous studies on the roles of microglia mainly focused on the neurotoxicity or neuroprotection of photoreceptors, while their contributions to synaptic remodeling of neuronal circuits in the retina of early RP remained unclarified. In the present study, we used Royal College of Surgeons (RCS) rats, a classic RP model characterized by progressive microglia activation and synapse loss, to investigate the constitutive effects of microglia on the synaptic lesions and ectopic neuritogenesis. Rod degeneration resulted in synapse disruption and loss in the outer plexiform layer (OPL) at the early stage of RP. Coincidentally, the resident microglia in the OPL increased phagocytosis and mainly engaged in phagocytic engulfment of postsynaptic mGluR6 of rod bipolar cells (RBCs). Complement pathway might be involved in clearance of postsynaptic elements of RBCs by microglia. We pharmacologically deleted microglia using a CSF1 receptor (CSF1R) inhibitor to confirm this finding, and found that it caused the accumulation of postsynaptic mGluR6 levels and increased the number and length of ectopic dendrites in the RBCs. Interestingly, the numbers of presynaptic sites expressing CtBP2 and colocalized puncta in the OPL of RCS rats were not affected by microglia elimination. However, sustained microglial depletion led to progressive functional deterioration in the retinal responses to light in RCS rats. Based on our results, microglia mediated the remodeling of RBCs by phagocytosing postsynaptic materials and inhibiting ectopic neuritogenesis, contributing to delay the deterioration of vision at the early stage of RP.

Indexed as

AnimalsDisease Models, AnimalEye ProteinsMicrogliaRatsReceptors, Granulocyte-Macrophage Colony-Stimulating FactorReceptors, Metabotropic GlutamateRetinaRetinal Photoreceptor Cell Outer SegmentRetinitis PigmentosaSynapsesCtbp2 protein, ratEye Proteinsmetabotropic glutamate receptor 6Receptors, Granulocyte-Macrophage Colony-Stimulating FactorReceptors, Metabotropic Glutamateectopic neuritogenesismicrogliaretinitis pigmentosarod bipolar cellsynapse

Identifiers

PMID31105708
PMCPMC6499027
OpenAlexW2942240528

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.