Evidence map›Paper›PMID 25880093›Full record

ArticleCell death & disease2015

Loss of CD147 results in impaired epithelial cell differentiation and malformation of the meibomian gland.

J Mauris, J Dieckow, S Schob, B Pulli, M P Hatton, S Jeong, A Bauskar, E Gabison, R Nowak, P Argüeso

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

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  12. Genetically modified laboratory mice with sebaceous glands abnormalities.Cellular and molecular life sciences : CMLS · 2016
    Review
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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

10 authors at 9 institutions in 2 countries.

J MaurisSchepens Eye Research Institute and Massachusetts Eye and Ear, Harvard Medical School, Boston, MA, USA.
J DieckowSchepens Eye Research Institute and Massachusetts Eye and Ear, Harvard Medical School, Boston, MA, USA.
S SchobCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
B PulliCenter for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
M P Hatton1] Schepens Eye Research Institute and Massachusetts Eye and Ear, Harvard Medical School, Boston, MA, USA [2] Ophthalmic Consultants of Boston, Boston, MA, USA.
S JeongInstitute for Genetic Medicine and Department of Ophthalmology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
A BauskarInstitute for Genetic Medicine and Graduate Program in Medical Biology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
E GabisonCornea and External Diseases, Fondation A. De Rothschild, Hôpital Bichat, APHP, Université Paris VII Diderot, Paris, France.
R NowakDepartment of Animal Sciences, University of Illinois, Urbana, IL, USA.
P ArgüesoSchepens Eye Research Institute and Massachusetts Eye and Ear, Harvard Medical School, Boston, MA, USA.
University of Southern California · USCenter for Systems Biology · USHarvard University · USHôpital Bichat-Claude-Bernard · FRMassachusetts Eye and Ear Infirmary · USMassachusetts General Hospital · USOphthalmic Consultants of Boston · USSmith-Kettlewell Eye Research Institute · USUniversity of Illinois Urbana-Champaign · US

Funding

O-Glycans on Mucins at the Ocular SurfaceR01EY014847 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI ARGUESO, PABLO · 2003 to 2014
$4.0M
CD147 and Corneal Wound RepairR01EY024031 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI ARGUESO, PABLO · 2015 to 2019
$2.4M
NEI NIH HHS EY014847NEI NIH HHS EY024031NEI NIH HHS R01 EY014847NEI NIH HHS R01 EY024031
6 · The paper itself

Abstract

Meibomian gland dysfunction is a leading cause of ocular surface disease. However, little is known about the regulatory processes that control the development and maintenance of this sebaceous gland. Here, we identify a novel function for CD147, a transmembrane protein that promotes tissue remodeling through induction of matrix metalloproteinases, in regulating meibocyte differentiation and activity. We found that CD147 localized along basal cells and within discrete membrane domains of differentiated meibocytes in glandular acini containing gelatinolytic activity. Induction of meibocyte differentiation in vitro promoted CD147 clustering and MMP9 secretion, whereas RNAi-mediated abrogation of CD147 impaired MMP9 secretion, concomitant with a reduction in the number of proliferative cells and cytoplasmic lipids. Meibomian glands of CD147 knockout mice had a lower number of acini in both the superior and inferior tarsal plates of the eyelids, and were characterized by loss of lipid-filled meibocytes compared with control mice. Together, our data provide evidence showing that gelatinolytic activity in meibocytes is dependent on CD147, and supports a role for CD147 in maintaining the normal development and function of the meibomian gland.

Indexed as

AnimalsBasiginCell DifferentiationCell ProliferationEpithelial CellsHumansMeibomian GlandsMiceMice, Inbred C57BLMice, KnockoutBasigin

Identifiers

PMID25880093
PMCPMC4650560
OpenAlexW2025323821

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.