Evidence map›Paper›PMID 21217103›Full record

ArticleInvestigative ophthalmology & visual science2011

Cadm1 expression and function in the mouse lens.

Alicia De Maria, Yanrong Shi, Xianmin Luo, Louise Van Der Weyden, Steven Bassnett

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The lens growth process.Progress in retinal and eye research · 2017
    Review
  6. Birc7: A Late Fiber Gene of the Crystalline Lens.Investigative ophthalmology & visual science · 2015
    Article
  7. Review
  8. Article
  9. Article
  10. Further analysis of the lens phenotype in Lim2-deficient mice.Investigative ophthalmology & visual science · 2011
    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 1 institution in 1 country.

Alicia De MariaDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri, USA.
Yanrong Shi
Xianmin Luo
Louise Van Der Weyden
Steven Bassnett
Wellcome Sanger Institute · GB

Funding

WASHINGTON UNIVERSITY CENTER VISION RESEARCHP30EY002687 · NEI · WASHINGTON UNIVERSITY · PI Philip Andrew Ruzycki · 1985 to 2026
$18.4M
FIBER CELL FORMATION IN NORMAL AND CATARACTOUS LENSESR01EY009852 · NEI · WASHINGTON UNIVERSITY · PI BASSNETT, STEVEN · 1992 to 2021
$7.8M
LIM2 AND THE LENS CORE SYNCYTIUMR01EY018185 · NEI · WASHINGTON UNIVERSITY · PI BASSNETT, STEVEN · 2008 to 2012
$1.9M
NEI NIH HHS EY009852NEI NIH HHS P30 EY002687NEI NIH HHS P30EY002687NEI NIH HHS R01 EY009852NEI NIH HHS R01 EY018185NEI NIH HHS R01EY018185Wellcome Trust
6 · The paper itself

Abstract

purposeThe immunoglobulin superfamily member Cadm1 is a single-pass, type 1 membrane protein that mediates calcium-independent, cell-cell adhesion. Cadm1 has been implicated in tumor formation and synaptogenesis. A recent analysis of mouse lens cell membranes identified Cadm1 as a major constituent of the fiber cell membrane proteome. Here the authors examined the expression and function of Cadm1 in the mouse lens.

methodsCadm1 expression was analyzed by Western blotting and immunofluorescence. The morphology of individual wild-type and Cadm1-null lens cells was visualized by confocal microscopy.

resultsCadm1 was present in epithelial and superficial fiber cells as a heavily glycosylated protein with an apparent molecular mass of ≈80 kDa. Analysis of proteins extracted from various strata of the lens indicated that Cadm1 was degraded during fiber cell differentiation, at approximately the same time as the lens organelles, an observation confirmed by confocal microscopy. In epithelial cells, Cadm1 was enriched in basolateral membranes, whereas, in fiber cells, expression was restricted to the lateral membranes. Lenses from Cadm1-null mice were of normal size and transparency. The three-dimensional morphology of the cells in the epithelial layer was unaltered in the absence of Cadm1. However, in contrast to wild-type lens fiber cells, Cadm1-null fiber cells had an irregular, highly undulating morphology.

conclusionsCadm1 is an abundant component of the lens fiber cell membrane. Although not essential for lens transparency, Cadm1 has an indispensable role in establishing and maintaining the characteristic three-dimensional architecture of the lens fiber cell mass.

Indexed as

AnimalsBasement MembraneBlotting, WesternCell Adhesion Molecule-1Cell Adhesion MoleculesCell DifferentiationElectrophoresis, Polyacrylamide GelFluorescent Antibody Technique, IndirectImmunoglobulinsLens, CrystallineMiceMice, Inbred C57BLMice, KnockoutMicroscopy, ConfocalRNA, MessengerCadm1 protein, mouseCell Adhesion Molecule-1Cell Adhesion MoleculesImmunoglobulinsRNA, Messenger

Identifiers

PMID21217103
PMCPMC3080734
OpenAlexW2085541258

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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.