Evidence map›Paper›PMID 25684979›Full record

ArticleMolecular vision2015

Chondrogenesis in scleral stem/progenitor cells and its association with form-deprived myopia in mice.

Pei-Chang Wu, Chia-Ling Tsai, Gabriel M Gordon, Shinwu Jeong, Tatsuo Itakura, Nitin Patel, Songtao Shi, M Elizabeth Fini

Open access · greenAbstract read
In one paragraph

Article in Molecular vision, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

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  16. Scleral hypoxia is a target for myopia control.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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

8 authors at 3 institutions in 2 countries.

Pei-Chang WuDepartment of Ophthalmology, Kaohsiung Chang Gung Memorial Hospital, and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Chia-Ling TsaiDepartment of Dentistry, Kaohsiung Chang Gung Memorial Hospital, and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Gabriel M GordonUSC Institute for Genetic Medicine, University of Southern California, Los Angeles, CA.
Shinwu JeongUSC Institute for Genetic Medicine, University of Southern California, Los Angeles, CA ; Department of Ophthalmology, University of Southern California, Los Angeles, CA.
Tatsuo ItakuraUSC Institute for Genetic Medicine, University of Southern California, Los Angeles, CA.
Nitin PatelUSC Institute for Genetic Medicine, University of Southern California, Los Angeles, CA.
Songtao ShiDepartment of Anatomy and Cell Biology, University of Pennsylvania, School of Dental Medicine, Philadelphia, PA.
M Elizabeth FiniUSC Institute for Genetic Medicine, University of Southern California, Los Angeles, CA ; Department of Ophthalmology, University of Southern California, Los Angeles, CA ; Department of Cell & Neurobiology, Keck School of Medicine of USC, University of Southern California, Los Angeles, CA.
Chang Gung University · TWKaohsiung Chang Gung Memorial Hospital · TWUniversity of Southern California · US

Funding

TRANSITION TO THE REPAIR FIBROBLAST PHENOTYPER01EY009828 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI FINI, M ELIZABETH · 1994 to 2011
$3.7M
NEI NIH HHS R01 EY009828NEI NIH HHS R01EY09828
6 · The paper itself

Abstract

purposePreviously, we demonstrated that scleral stem/progenitor cells (SSPCs) from mice have a chondrogenic differentiation potential, which is stimulated by transforming growth factor-β (TGF-β). In the present study, we hypothesized that chondrogenesis in the sclera could be a possible mechanism in myopia development. Therefore, we investigated the association of form-deprivation myopia (FDM) with expressions in mice sclera representing the chondrogenic phenotype: collagen type II (Col2) and α-smooth muscle actin (α-SMA).

methodsThe mRNA levels of α-SMA and Col2 in cultured murine SSPCs during chondrogenesis stimulated by TGF-β2 were determined by real-time quantitative RT-PCR (qRT-PCR). The expression patterns of α-SMA and Col2 were assessed by immunohistochemistry in a three dimensional pellet culture. In an FDM mouse model, a western blot analysis and immunofluorescence study were used to detect the changes in the α-SMA and Col2 protein expressions in the sclera. In the RPE-choroid complex, qRT-PCR was used to detect any changes in the TGF-β mRNA expression.

resultsThe treatment of SSPCs in vitro with TGF-β2 for 24 h at 1 or 10 ng/ml led to increased levels of both the α-SMA and Col2 expressions. In addition, we observed the formation of cartilage-like pellets from TGF-β2-treated SSPCs. Both α-SMA and Col2 were expressed in the pellet. In an in-vivo study, the α-SMA and Col2 protein expressions were significantly increased in the sclera of FDM eyes in comparison to contralateral control eyes. Similarly, the levels of TGF-β in the RPE-choroid complex of an FDM eye were also significantly elevated.

conclusionBased on the concept of stem cells possessing multipotent differentiation potentials, scleral chondrogenesis induced by SSPCs may play a role in myopia development. The increased expressions of the cartilage-associated proteins Col2 and α-SMA during scleral chondrogenesis may be potential markers for myopia development. In addition, the increased levels of TGF-β mRNA in the RPE-choroid complex might induce the chondrogenic change in the sclera during myopia development.

Indexed as

ActinsAnimalsCells, CulturedChondrogenesisChoroidCollagen Type IIDisease Models, AnimalGene ExpressionMaleMiceMice, Inbred C57BLMyopiaRetinal Pigment EpitheliumRNA, MessengerScleraStem CellsActinsalpha-smooth muscle actin, mouseCollagen Type IIRNA, MessengerTgfb2 protein, mouseTransforming Growth Factor betaTransforming Growth Factor beta2

Identifiers

PMID25684979
PMCPMC4323720
OpenAlexW2215841289

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.