Evidence map›Paper›PMID 33008127›Full record

ArticleInternational journal of molecular sciences2020

Pigment Epithelium-Derived Factor (PEDF) Fragments Prevent Mouse Cone Photoreceptor Cell Loss Induced by Focal Phototoxicity In Vivo.

Francisco J Valiente-Soriano, Johnny Di Pierdomenico, Diego García-Ayuso, Arturo Ortín-Martínez, Juan A Miralles de Imperial-Ollero, Alejandro Gallego-Ortega, Manuel Jiménez-López, M Paz Villegas-Pérez, S Patricia Becerra, Manuel Vidal-Sanz

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Pigment Epithelium-Derived Factor (PEDF)-Based Therapy Induced Photoreceptor Survival by Stabilizing Choroidal Neovessels in a VEGF Overexpression CNV Rat Model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  17. Delivery Systems of Retinoprotective Proteins in the Retina.International journal of molecular sciences · 2021
    Review
  18. 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 at 3 institutions in 3 countries.

Francisco J Valiente-SorianoDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.
Johnny Di PierdomenicoDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.ORCID 0000-0001-9124-9247
Diego García-AyusoDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.ORCID 0000-0002-7639-5366
Arturo Ortín-MartínezDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.ORCID 0000-0003-0492-6604
Juan A Miralles de Imperial-OlleroDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.
Alejandro Gallego-OrtegaDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.
Manuel Jiménez-LópezDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.
M Paz Villegas-PérezDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.ORCID 0000-0002-5734-482X
S Patricia BecerraSection of Protein Structure and Function, NEI-NIH, Bethesda, MD 20892-0608, USA.ORCID 0000-0001-8004-4983
Manuel Vidal-SanzDepartamento de Oftalmología, Facultad de Medicina, Universidad de Murcia, e Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca (IMIB-Arrixaca), 30.120 Murcia, Spain.ORCID 0000-0002-9216-1615
Instituto Murciano de Investigación Biosanitaria · ESNational Institutes of Health · USUniversity Health Network · CA

Funding

Fundación Séneca, Agencia de Ciencia y Tecnología Región de Murcia 19881/GERM/15Intramural Research Program of the National Eye Institute, NIH, U.S.A. #EY000306Spanish Ministry of Economy and Competitiveness, Instituto de Salud Carlos III, Fondo Europeo de Desarrollo Regional "Una manera de hacer Europa" PI19/00203Spanish Ministry of Economy and Competitiveness, Instituto de Salud Carlos III, Fondo Europeo de Desarrollo Regional "Una manera de hacer Europa" RD16/0008/0026Spanish Ministry of Economy and Competitiveness, Instituto de Salud Carlos III, Fondo Europeo de Desarrollo Regional "Una manera de hacer Europa" SAF2015-67643-P
6 · The paper itself

Abstract

Here, we evaluated the effects of PEDF (pigment epithelium-derived factor) and PEDF peptides on cone-photoreceptor cell damage in a mouse model of focal LED-induced phototoxicity (LIP) in vivo. Swiss mice were dark-adapted overnight, anesthetized, and their left eyes were exposed to a blue LED placed over the cornea. Immediately after, intravitreal injection of PEDF, PEDF-peptide fragments 17-mer, 17-mer[H105A] or 17-mer[R99A] (all at 10 pmol) were administered into the left eye of each animal. BDNF (92 pmol) and bFGF (27 pmol) injections were positive controls, and vehicle negative control. After 7 days, LIP resulted in a consistent circular lesion located in the supratemporal quadrant and the number of S-cones were counted within an area centered on the lesion. Retinas treated with effectors had significantly greater S-cone numbers (PEDF (60%), 17-mer (56%), 17-mer [H105A] (57%), BDNF (64%) or bFGF (60%)) relative to their corresponding vehicle groups (≈42%). The 17-mer[R99A] with no PEDF receptor binding and no neurotrophic activity, PEDF combined with a molar excess of the PEDF receptor blocker P1 peptide, or with a PEDF-R enzymatic inhibitor had undetectable effects in S-cone survival. The findings demonstrated that the cone survival effects were mediated via interactions between the 17-mer region of the PEDF molecule and its PEDF-R receptor.

Indexed as

AnimalsCorneaDermatitis, PhototoxicDisease Models, AnimalEye ProteinsHumansMiceNerve Growth FactorsPeptide FragmentsPeptidesPhotoperiodPigment Epithelium-Derived FactorReceptors, NeuropeptideRetinaRetinal Cone Photoreceptor CellsSerpinsEye ProteinsNerve Growth FactorsPeptide FragmentsPeptidesPigment Epithelium-Derived Factorpigment epithelium-derived factor receptorReceptors, NeuropeptideSerpinsadult miceBDNFbFGFcone-photoreceptorin vivo neuroprotectionin vivo phototoxicity modelPEDFPEDF fragment 17-merPEDF fragment 17-mer[H105A]

Identifiers

PMID33008127
PMCPMC7582775
OpenAlexW3090669454

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.