Evidence map›Paper›PMID 28866025›Full record

ReviewVision research2017

Müller cells and diabetic retinopathy.

Brandon A Coughlin, Derrick J Feenstra, Susanne Mohr

Open access · greenAbstract readReview
In one paragraph

Review in Vision research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 201 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
201citing papers in PubMed, 1 pooled it
13.7field-weighted citation impact, top 1% 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

201 citing papers in PubMed, 1 synthesis or guideline pooled it, 334 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Regulation of Glutathione Peroxidase 4 in Diabetic Retinopathy.International journal of molecular sciences · 2026
    Article
  4. Review
  5. Article
  6. Neuroprotection in Early Diabetic Retinal Disease Using Eyedrop Delivery.International journal of molecular sciences · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Ethnic comparison of MacTel over 5 years follow up.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Observational
  15. Article
  16. Article
  17. Review
  18. Acrolein Promotes Retinal Inflammation Through Macrophage Chemotaxis by Inducing CCL2 Production From Müller Cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  19. Article
  20. Review

141 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Brandon A CoughlinDepartment of Physiology, Michigan State University, East Lansing, MI, USA.
Derrick J FeenstraDepartment of Physiology, Michigan State University, East Lansing, MI, USA.
Susanne MohrDepartment of Physiology, Michigan State University, East Lansing, MI, USA. Electronic address: mohrs@msu.edu.
Michigan State University · US

Funding

Targeting the IGF-1 System in Retinal AngiogenesisR01EY007739 · NEI · UNIVERSITY OF FLORIDA · PI ABCOUWER, STEVEN F, GRANT, MARIA BARTOLOMEO · 1995 to 2015
$5.4M
IL-1 beta Signaling in Diabetic RetinopathyR01EY017206 · NEI · MICHIGAN STATE UNIVERSITY · PI MOHR, SUSANNE · 2006 to 2010
$1.5M
Retinal Cell Death in Diabetic RetinopathyR03EY014380 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI MOHR, SUSANNE · 2004 to 2006
$455k
IL-10 and Diabetic RetinopathyR21EY024757 · NEI · MICHIGAN STATE UNIVERSITY · PI MOHR, SUSANNE · 2014 to 2015
$406k
NEI NIH HHS R01 EY007739NEI NIH HHS R01 EY017206NEI NIH HHS R03 EY014380NEI NIH HHS R21 EY024757
6 · The paper itself

Abstract

Müller cells are one of the primary glial cell types found in the retina and play a significant role in maintaining retinal function and health. Since Müller cells are the only cell type to span the entire width of the retina and have contact to almost every cell type in the retina they are uniquely positioned to perform a wide variety of functions necessary to maintaining retinal homeostasis. In the healthy retina, Müller cells recycle neurotransmitters, prevent glutamate toxicity, redistribute ions by spatial buffering, participate in the retinoid cycle, and regulate nutrient supplies by multiple mechanisms. Any disturbance to the retinal environment is going to influence proper Müller cell function and well being which in turn will affect the entire retina. This is evident in a disease like diabetic retinopathy where Müller cells contribute to neuronal dysfunction, the production of pro-angiogenic factors leading to neovascularization, the set up of a chronic inflammatory retinal environment, and eventual cell death. In this review, we highlight the importance of Müller cells in maintaining a healthy and functioning retina and discuss various pathological events of diabetic retinopathy in which Müller cells seem to play a crucial role. The beneficial and detrimental effects of cytokine and growth factor production by Müller cells on the microvasculature and retinal neuronal tissue will be outlined. Understanding Müller cell functions within the retina and restoring such function in diabetic retinopathy should become a cornerstone for developing effective therapies to treat diabetic retinopathy.

Indexed as

AnimalsCytokinesDiabetic RetinopathyEpendymoglial CellsHumansIntercellular Signaling Peptides and ProteinsCytokinesIntercellular Signaling Peptides and ProteinsCell deathDiabetic retinopathyMüller cellsRetinal inflammation

Identifiers

PMID28866025
PMCPMC5794018
OpenAlexW2753138435

What OpenQuestion holds

Textmetadata
LicenceTDM
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.