Evidence map›Paper›PMID 32232350›Full record

ArticleInvestigative ophthalmology & visual science2020

Utility of LysM-cre and Cdh5-cre Driver Mice in Retinal and Brain Research: An Imaging Study Using tdTomato Reporter Mouse.

Abdelrahman Y Fouda, Zhimin Xu, S Priya Narayanan, R William Caldwell, Ruth B Caldwell

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. The neuroimmune interface in retinal regeneration.Progress in retinal and eye research · 2025
    Review
  3. Rescue of cochlear vascular pathology prevents sensory hair cell loss in Norrie disease.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Article
  5. Article
  6. SOCS3 regulates pathological retinal angiogenesis through modulating SPP1 expression in microglia and macrophages.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Deletion of Socs3 in LysMMolecular neurodegeneration · 2021
    Article
  16. Article
  17. Arginase 1 Insufficiency Precipitates Amyloid-Frontiers in immunology · 2020
    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

5 authors at 3 institutions in 1 country.

Abdelrahman Y Fouda, Augusta University, Augusta, Georgia.
Zhimin Xu, Augusta University, Augusta, Georgia.
S Priya Narayanan, Augusta University, Augusta, Georgia.
R William Caldwell, Augusta University, Augusta, Georgia.
Ruth B Caldwell, Augusta University, Augusta, Georgia.
Augusta University Health · USCharlie Norwood VA Medical Center · USDiscovery Institute · US

Funding

Cellular Mechanisms of Retinopathy: Role of ArginaseR01EY011766 · NEI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI CALDWELL, ROBERT WILLIAM, CALDWELL, RUTH B · 1998 to 2021
$6.7M
Myeloid glycolysis in pathological ocular angiogenesisR01EY030500 · NEI · AUGUSTA UNIVERSITY · PI CALDWELL, RUTH B, HUO, YUQING · 2019 to 2023
$2.6M
Mechanisms of neurodegeneration in diabetic retinopathy: Role of spermine oxidaseR01EY028569 · NEI · UNIVERSITY OF GEORGIA · PI NARAYANAN, PRIYA · 2018 to 2023
$1.8M
Role of Arginase 1 in Retinal Ischemia-Reperfusion InjuryK99EY029373 · NEI · AUGUSTA UNIVERSITY · PI FOUDA, ABDELRAHMAN · 2019 to 2020
$233k
Mechanisms of Diabetic Retinopathy: Oxidative Stress and InflammationI01BX001233 · VA · CHARLIE NORWOOD VA MEDICAL CENTER · PI CALDWELL, RUTH B · 2012 to 2015
–
BLR&D Research Career Scientist Award ApplicationIK6BX005228 · VA · CHARLIE NORWOOD VA MEDICAL CENTER · PI CALDWELL, RUTH B · 2020 to 2021
–
Mechanisms of Traumatic Retinal Injury: Targeting the Arginase PathwayI01BX003221 · VA · CHARLIE NORWOOD VA MEDICAL CENTER · PI CALDWELL, RUTH B · 2016 to 2019
–
BLRD VA I01 BX001233BLRD VA I01 BX003221BLRD VA IK6 BX005228NEI NIH HHS K99 EY029373NEI NIH HHS R01 EY011766NEI NIH HHS R01 EY028569NEI NIH HHS R01 EY030500
6 · The paper itself

Abstract

Purpose: The lysozyme 2 (Lyz2 or LysM) cre mouse is extensively used to achieve genetic manipulation in myeloid cells and it has been widely employed in retinal research. However, LysM has been recently described to be expressed in brain neurons and there is a debate on whether it is also expressed by resident microglia in addition to infiltrating macrophages. Methods: We examined LysM-cre recombination in retinal tissue using a LysM-cre/tdTomato reporter mouse together with immunolabeling for several retinal cell markers. We further compared LysM-cre tdTomato recombination with that of Cdh5-cre driver, which is expressed in both endothelial and hematopoietic cells. Results: LysM-cre was strongly expressed in most microglia/resident macrophages in neonatal retinas (P8) and to a lesser extent in microglia of adult retinas. In addition, there was some neuronal recombination (8 %) of LysM-cre specifically in adult retinal ganglion cells and amacrine cells. After retinal ischemia-reperfusion injury, LysM-cre was strongly expressed in microglia/infiltrating macrophages. Cdh5-cre was expressed in endothelial and myeloid cells of P8 pups retinas. Unexpectedly, Cdh5 showed additional expression in adult mouse retinal ganglion cells and brain neurons. Conclusions: LysM-cre is expressed in macrophages and a subset of microglia together with a small but significant recombination of LysM-cre in the retinal neurons of adult mice. Cdh5 also showed some neuronal expression in both retina and brain of adult mice. These findings should be taken into consideration when interpreting results from central nervous system research using LysM-cre and Cdh5-cre mice.

Indexed as

AnimalsAnimals, NewbornAntigens, CDBiomedical ResearchBrainCadherin 5CadherinsDiagnostic ImagingEndothelium, VascularFemaleGenes, ReporterIntegrasesLuminescent AgentsLuminescent ProteinsMacrophagesMaleAntigens, CDCadherin 5CadherinsCre recombinaseIntegrasesLuminescent AgentsLuminescent Proteinslysozyme M, mouseMuramidaseRed Fluorescent Protein

Identifiers

PMID32232350
PMCPMC7405957
OpenAlexW3013966802

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.