Evidence map›Paper›PMID 9391089›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

Conservation of fibroblast growth factor function in lens regeneration.

K Del Rio-Tsonis, J C Jung, I M Chiu, P A Tsonis

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

25 citing papers in PubMed, 96 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Lens regeneration: a historical perspective.The International journal of developmental biology · 2018
    Review
  10. Article
  11. Cell signaling pathways in vertebrate lens regeneration.Current topics in microbiology and immunology · 2013
    Review
  12. Article
  13. Article
  14. Molecular and cellular aspects of amphibian lens regeneration.Progress in retinal and eye research · 2010
    Article
  15. Review
  16. Gene expression profiles of lens regeneration and development in Xenopus laevis.Developmental dynamics : an official publication of the American Association of Anatomists · 2009
    Article
  17. Article
  18. An essential role for FGF receptor signaling in lens development.Seminars in cell & developmental biology · 2006
    Review
  19. Signaling during lens regeneration.Seminars in cell & developmental biology · 2006
    Review
  20. The role of Pax-6 in lens regeneration.Proceedings of the National Academy of Sciences of the United States of America · 2006
    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

4 authors at 2 institutions in 1 country.

K Del Rio-TsonisLaboratory of Molecular Biology, Department of Biology, University of Dayton, Dayton, OH 45469, USA.
J C Jung
I M Chiu
P A Tsonis
The Ohio State University · USUniversity of Dayton · US

Funding

GENE REGULATION IN LENS REGENERATIONR01EY010540 · NEI · UNIVERSITY OF DAYTON · PI TSONIS, PANAGIOTIS A · 1995 to 2013
$3.3M
NEI NIH HHS EY10540NEI NIH HHS R01 EY010540
6 · The paper itself

Abstract

In urodele amphibians, lens induction during development and regeneration occurs through different pathways. During development, the lens is induced from the mutual interaction of the ectoderm and the optic vesicle, whereas after lentectomy the lens is regenerated through the transdifferentiation of the iris-pigmented epithelial cells. Given the known role of fibroblast growth factors (FGFs) during lens development, we examined whether or not the expression and the effects of exogenous FGF during urodele lens regeneration were conserved. In this paper, we describe expression of FGF-1 and its receptors, FGFR-2 (KGFR and bek variants) and FGFR-3, in newts during lens regeneration. Expression of these genes was readily observed in the dedifferentiating pigmented epithelial cells, and the levels of expression were high in the lens epithelium and the differentiating fibers and lower in the retina. These patterns of expression implied involvement of FGFs in lens regeneration. To further elucidate this function, we examined the effects of exogenous FGF-1 and FGF-4 during lens regeneration. FGF-1 or FGF-4 treatment in lentectomized eyes resulted in the induction of abnormalities reminiscent to the ones induced during lens development in transgenic mice. Effects included transformation of epithelial cells to fiber cells, double lens regeneration, and lenses with abnormal polarity. These results establish that FGF molecules are key factors in fiber differentiation, polarity, and morphogenesis of the lens during regeneration even though the regenerating lens is induced by a different mechanism than in lens development. In this sense, FGF function in lens regeneration and development should be regarded as conserved. Such conservation should help elucidate the mechanisms of lens regeneration in urodeles and its absence in higher vertebrates.

Indexed as

Protein-Tyrosine KinasesAnimalsFibroblast Growth Factor 1Fibroblast Growth Factor 4Fibroblast Growth FactorsGene ExpressionImmunohistochemistryIn Situ HybridizationLens, CrystallineMiceProto-Oncogene ProteinsReceptor, Fibroblast Growth Factor, Type 2Receptor, Fibroblast Growth Factor, Type 3Receptor Protein-Tyrosine KinasesReceptors, Fibroblast Growth FactorRegenerationFgf4 protein, mouseFgfr2 protein, mouseFgfr3 protein, mouseFibroblast Growth Factor 1Fibroblast Growth Factor 4Fibroblast Growth FactorsProtein-Tyrosine KinasesProto-Oncogene ProteinsReceptor, Fibroblast Growth Factor, Type 2Receptor, Fibroblast Growth Factor, Type 3Receptor Protein-Tyrosine KinasesReceptors, Fibroblast Growth Factor

Identifiers

PMID9391089
PMCPMC28369
OpenAlexW2151575857

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.