Evidence map›Paper›PMID 27878997›Full record

ReviewGlia2017

Corneal epithelial cells function as surrogate Schwann cells for their sensory nerves.

Mary Ann Stepp, Gauri Tadvalkar, Raymond Hakh, Sonali Pal-Ghosh

Abstract readReview
In one paragraph

Review in Glia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
12.1field-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

73 citing papers in PubMed, 120 citations in OpenAlex.

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  12. CD4Proceedings of the National Academy of Sciences of the United States of America · 2024
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13 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

4 authors at 1 institution in 1 country.

Mary Ann SteppDepartment of Anatomy and Regenerative Biology, George Washington University Medical School, Washington, DC.ORCID 0000-0001-5623-2538
Gauri TadvalkarDepartment of Anatomy and Regenerative Biology, George Washington University Medical School, Washington, DC.
Raymond HakhDepartment of Anatomy and Regenerative Biology, George Washington University Medical School, Washington, DC.
Sonali Pal-GhoshDepartment of Anatomy and Regenerative Biology, George Washington University Medical School, Washington, DC.
George Washington University · US

Funding

Molecular mechanisms of corneal recurrent erosion formationR01EY008512 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI STEPP, MARY ANN · 1990 to 2024
$11.7M
NEI NIH HHS R01 EY008512
6 · The paper itself

Abstract

The eye is innervated by neurons derived from both the central nervous system and peripheral nervous system (PNS). While much is known about retinal neurobiology and phototransduction, less attention has been paid to the innervation of the eye by the PNS and the roles it plays in maintaining a functioning visual system. The ophthalmic branch of the trigeminal ganglion contains somas of neurons that innervate the cornea. These nerves provide sensory functions for the cornea and are referred to as intraepithelial corneal nerves (ICNs) consisting of subbasal nerves and their associated intraepithelial nerve terminals. ICNs project for several millimeters within the corneal epithelium without Schwann cell support. Here, we present evidence for the hypothesis that corneal epithelial cells function as glial cells to support the ICNs. Much of the data supporting this hypothesis is derived from studies of corneal development and the reinnervation of the ICNs in the rodent and rabbit cornea after superficial wounds. Corneal epithelial cells activate in response to injury via mechanisms similar to those induced in Schwann cells during Wallerian Degeneration. Corneal epithelial cells phagocytize distal axon fragments within hours of ICN crush wounds. During aging, the proteins, lipids, and mitochondria within the ICNs become damaged in a process exacerbated by UV light. We propose that ICNs shed their aged and damaged termini and continuously elongate to maintain their density. Available evidence points to new unexpected roles for corneal epithelial cells functioning as surrogate Schwann cells for the ICNs during homeostasis and in response to injury. GLIA 2017;65:851-863.

Indexed as

AnimalsEpithelium, CornealHumansPeripheral Nervous SystemSchwann CellsSensory Receptor Cellscorneacorneal nervesepitheliumperipheral nervous systemSchwann cellswound response

Identifiers

PMID27878997
PMCPMC5395310
OpenAlexW2552623886

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.