Evidence map›Paper›PMID 12692670›Full record

ArticleHistochemistry and cell biology2003

Cellular distribution of lens epithelium-derived growth factor (LEDGF) in the rat eye: loss of LEDGF from nuclei of differentiating cells.

Eri Kubo, Dhirendra P Singh, Nigar Fatma, Toshimichi Shinohara, Peggy Zelenka, Venkat N Reddy, Leo T Chylack

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In one paragraph

Article in Histochemistry and cell biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

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  19. Cell death in health and disease.Journal of cellular and molecular medicine
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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

7 authors at 4 institutions in 1 country.

Eri KuboThe Center for Ophthalmic Research, Brigham and Women's Hospital, Havard Medical School, 221 Longwood Avenue, Boston, MA 02115, USA.
Dhirendra P Singh
Nigar Fatma
Toshimichi Shinohara
Peggy Zelenka
Venkat N Reddy
Leo T Chylack
Brigham and Women's Hospital · USUniversity of Nebraska Medical Center · USNational Institutes of Health · USUniversity of Michigan–Ann Arbor · US

Funding

Gene regulation by LEDGFR01EY013394 · NEI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SINGH, DHIRENDRA P · 2002 to 2012
$3.0M
LENS EPITHELIAL CELL DERIVED GROWTH FACTORR01EY012015 · NEI · BRIGHAM AND WOMEN'S HOSPITAL · PI CHYLACK, LEO T · 1998 to 2000
$295k
PROMOTER AND REGULATORY FACTORS OF THE ARRESTIN GENER01EY010824 · NEI · BRIGHAM AND WOMEN'S HOSPITAL · PI SHINOHARA, TOSHIMICHI · 1995 to 1998
–
NEI NIH HHS EY07003NEI NIH HHS EY10824NEI NIH HHS EY12015NEI NIH HHS EY13394
6 · The paper itself

Abstract

Lens epithelium-derived growth factor (LEDGF) enhances the survival and growth of cells. To understand LEDGF's spatial localization and its putative function(s) during proliferation and differentiation, we localized LEDGF during terminal differentiation in whole rat lenses, lens epithelial cell (LEC) explants stimulated with FGF-2, and insulin, iris, human LECs with lentoids. In addition, intracellular localization of LEDGF was performed in other ocular tissues: ciliary body, retina, and cornea. We found the immunopositivity of nuclear LEDGF decreased in LECs of the equatorial region. In contrast, immunopositivity of LEDGF was detected in the cytoplasm of LECs and superficial fiber cells. After treating LEC explants with FGF-2 and insulin, which are known to be differentiating factors for LECs, the nuclei of these cells showed no LEDGF immunopositivity, but explants did express p57(kip2), a differentiation marker protein. Also, immunopositive LEDGF was not detected in the nuclei of differentiated cells, lentoid body, and corneal epithelial cells. This demonstrated that the loss of LEDGF from the nucleus may be associated with the process of terminal differentiation that might be in some way common with the biochemical mechanisms of apoptosis. The spatial and temporal distribution of LEDGF in the present study also provides a vision for further investigation as to how this protein is involved in cell fate determination.

Indexed as

AnimalsCell DifferentiationCell NucleusCells, CulturedCiliary BodyCorneaEpithelial CellsFibroblast Growth Factor 2HumansImmunoenzyme TechniquesIn Situ HybridizationInsulinIntercellular Signaling Peptides and ProteinsLens, CrystallineRatsRats, Sprague-DawleyFibroblast Growth Factor 2InsulinIntercellular Signaling Peptides and Proteinslens epithelium-derived growth factorRNA, Messenger

Identifiers

PMID12692670
OpenAlexW2117258794

What OpenQuestion holds

Textmetadata
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.