Evidence map›Paper›PMID 37624696›Full record

ArticleCell reports2023

Osteopontin drives retinal ganglion cell resiliency in glaucomatous optic neuropathy.

Mengya Zhao, Kenichi Toma, Benyam Kinde, Liang Li, Amit K Patel, Kong-Yan Wu, Matthew R Lum, Chengxi Tan, Jody E Hooper, Arnold R Kriegstein and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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  16. Monocyte Invasion into the Retina Restricts the Regeneration of Neurons from Müller Glia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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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

16 authors at 4 institutions in 1 country.

Mengya ZhaoDepartment of Ophthalmology, University of California San Francisco, San Francisco, CA 94158, USA.
Kenichi TomaDepartment of Ophthalmology, University of California San Francisco, San Francisco, CA 94158, USA.
Benyam KindeDepartment of Ophthalmology, University of California San Francisco, San Francisco, CA 94158, USA. Electronic address: bkinde@gmail.com.
Liang LiDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Amit K PatelViterbi Family Department of Ophthalmology, University of California San Diego, San Diego, CA 92037, USA.
Kong-Yan WuDepartment of Ophthalmology, University of California San Francisco, San Francisco, CA 94158, USA.
Matthew R LumDepartment of Ophthalmology, University of California San Francisco, San Francisco, CA 94158, USA.
Chengxi TanDepartment of Ophthalmology, University of California San Francisco, San Francisco, CA 94158, USA.
Jody E HooperDepartment of Pathology, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Arnold R KriegsteinDepartment of Neurology and The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California San Francisco, San Francisco, CA 94143, USA.
Anna La TorreDepartment of Cell Biology and Human Anatomy, University of California, Davis, Davis, CA 95616, USA.
Yaping Joyce LiaoDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Derek S WelsbieViterbi Family Department of Ophthalmology, University of California San Diego, San Diego, CA 92037, USA.
Yang HuDepartment of Ophthalmology, Stanford University School of Medicine, Palo Alto, CA 94304, USA. Electronic address: huyang@stanford.edu.
Ying HanDepartment of Ophthalmology, University of California San Francisco, San Francisco, CA 94158, USA. Electronic address: ying.han@ucsf.edu.
Xin DuanDepartment of Ophthalmology, University of California San Francisco, San Francisco, CA 94158, USA. Electronic address: xin.duan@ucsf.edu.
University of California, San Francisco · USStanford University · USUniversity of California, San Diego · USUniversity of California, Davis · US

Funding

Rapid-Prototyping and Design CoreP30EY002162 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAMBA, DEEPAK ASHOK · 1985 to 2024
$16.8M
Development and Expansion of the Human Cerebral CortexR35NS097305 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRIEGSTEIN, ARNOLD · 2017 to 2024
$8.5M
Stanford Vision Research CoreP30EY026877 · NEI · STANFORD UNIVERSITY · PI Jeffrey L Goldberg · 2017 to 2026
$8.0M
Elucidating Neuron-Intrinsic Molecular Mechanisms of Optic Nerve RegenerationR01EY024932 · NEI · TEMPLE UNIV OF THE COMMONWEALTH · PI Yang Hu · 2015 to 2026
$4.8M
Neuroprotection by Modulating ER Stress in GlaucomaR01EY023295 · NEI · TEMPLE UNIV OF THE COMMONWEALTH · PI HU, YANG · 2013 to 2022
$3.8M
Mechanisms Underlying Type II Cadherin Guided Assembly of Retinal CircuitsR01EY030138 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Xin Duan · 2020 to 2026
$3.2M
Kinase Multitargeting for Glaucoma NeuroprotectionR01EY029342 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Derek Stuart Welsbie · 2018 to 2026
$3.2M
In Vivo Function and Metabolism Evaluation of Glaucomatous RGCs by Two-Photon Scanning Laser OphthalmologyR01EY034353 · NEI · STANFORD UNIVERSITY · PI Yang Hu, Hao F Zhang · 2023 to 2026
$2.7M
Optineurin dysfunction induces neurodegeneration in normal tension glaucoma by a novel molecular mechanismR01EY032518 · NEI · STANFORD UNIVERSITY · PI Yang Hu · 2022 to 2026
$2.7M
Embryonic Stem Cell Approach to Retinal Ganglion Cell Replacement: an In Vivo StudyR01EY026942 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LA TORRE, ANNA · 2016 to 2020
$2.0M
NEI NIH HHS P30 EY002162NEI NIH HHS P30 EY026877NEI NIH HHS R01 EY023295NEI NIH HHS R01 EY024932NEI NIH HHS R01 EY026942NEI NIH HHS R01 EY029342NEI NIH HHS R01 EY030138NEI NIH HHS R01 EY032518NEI NIH HHS R01 EY034353NINDS NIH HHS R35 NS097305
6 · The paper itself

Abstract

Chronic neurodegeneration and acute injuries lead to neuron losses via diverse processes. We compared retinal ganglion cell (RGC) responses between chronic glaucomatous conditions and the acute injury model. Among major RGC subclasses, αRGCs and intrinsically photosensitive RGCs (ipRGCs) preferentially survive glaucomatous conditions, similar to findings in the retina subject to axotomy. Focusing on an αRGC intrinsic factor, Osteopontin (secreted phosphoprotein 1 [Spp1]), we found an ectopic neuronal expression of Osteopontin (Spp1) in other RGCs subject to glaucomatous conditions. This contrasted with the Spp1 downregulation subject to axotomy. αRGC-specific Spp1 elimination led to significant αRGC loss, diminishing their resiliency. Spp1 overexpression led to robust neuroprotection of susceptible RGC subclasses under glaucomatous conditions. In contrast, Spp1 overexpression did not significantly protect RGCs subject to axotomy. Additionally, SPP1 marked adult human RGC subsets with large somata and SPP1 expression in the aqueous humor correlated with glaucoma severity. Our study reveals Spp1's role in mediating neuronal resiliency in glaucoma.

Indexed as

GlaucomaOptic Nerve DiseasesHumansOptic NerveOsteopontinRetinal Ganglion CellsOsteopontinCP: Neuroscienceglaucomahuman retinaneuronal typesneuroprotectionoptic nerve crushOsteopontinretinal ganglion cell

Identifiers

PMID37624696
PMCPMC10591811
OpenAlexW4386112565

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.