Evidence map›Paper›PMID 26305099›Full record

ArticlePLoS genetics2015

Transient laminin beta 1a Induction Defines the Wound Epidermis during Zebrafish Fin Regeneration.

Chen-Hui Chen, Alexander F Merriman, Jeremiah Savage, Jason Willer, Taylor Wahlig, Nicholas Katsanis, Viravuth P Yin, Kenneth D Poss

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. 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
1.7field-weighted citation impact, top 17% 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, 44 citations in OpenAlex.

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  13. Voltage-gated sodium channelProceedings of the National Academy of Sciences of the United States of America · 2022
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  14. 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

8 authors at 2 institutions in 1 country.

Chen-Hui ChenDepartment of Cell Biology and Howard Hughes Medical Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
Alexander F MerrimanDepartment of Cell Biology and Howard Hughes Medical Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
Jeremiah SavageDepartment of Cell Biology and Howard Hughes Medical Institute, Duke University School of Medicine, Durham, North Carolina, United States of America; Center for Human Disease Modeling, Department of Cell Biology, Duke University, Durham, North Carolina, United States of America.
Jason WillerCenter for Human Disease Modeling, Department of Cell Biology, Duke University, Durham, North Carolina, United States of America.
Taylor WahligDepartment of Cell Biology and Howard Hughes Medical Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
Nicholas KatsanisCenter for Human Disease Modeling, Department of Cell Biology, Duke University, Durham, North Carolina, United States of America.
Viravuth P YinDepartment of Cell Biology and Howard Hughes Medical Institute, Duke University School of Medicine, Durham, North Carolina, United States of America; Davis Center for Regenerative Biology and Medicine, Mount Desert Island Biological Laboratory, Salisbury Cove, Maine, United States of America.
Kenneth D PossDepartment of Cell Biology and Howard Hughes Medical Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
Duke University · USHoward Hughes Medical Institute · US

Funding

Understanding the role of thyroid hormone signaling during axolotl limb regenerationP20GM104318 · NIGMS · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI DRUMMOND, IAIN A. · 2013 to 2023
$23.0M
Regulation of Appendage Regeneration in ZebrafishR01GM074057 · NIGMS · DUKE UNIVERSITY · PI POSS, KENNETH D · 2006 to 2017
$3.7M
NIGMS NIH HHS P20 GM104318NIGMS NIH HHS R01 GM074057
6 · The paper itself

Abstract

The first critical stage in salamander or teleost appendage regeneration is creation of a specialized epidermis that instructs growth from underlying stump tissue. Here, we performed a forward genetic screen for mutations that impair this process in amputated zebrafish fins. Positional cloning and complementation assays identified a temperature-sensitive allele of the ECM component laminin beta 1a (lamb1a) that blocks fin regeneration. lamb1a, but not its paralog lamb1b, is sharply induced in a subset of epithelial cells after fin amputation, where it is required to establish and maintain a polarized basal epithelial cell layer. These events facilitate expression of the morphogenetic factors shha and lef1, basolateral positioning of phosphorylated Igf1r, patterning of new osteoblasts, and regeneration of bone. By contrast, lamb1a function is dispensable for juvenile body growth, homeostatic adult tissue maintenance, repair of split fins, or renewal of genetically ablated osteoblasts. fgf20a mutations or transgenic Fgf receptor inhibition disrupt lamb1a expression, linking a central growth factor to epithelial maturation during regeneration. Our findings reveal transient induction of lamb1a in epithelial cells as a key, growth factor-guided step in formation of a signaling-competent regeneration epidermis.

Indexed as

RegenerationAmino Acid SequenceAnimal FinsAnimalsBase SequenceEpidermisFemaleFibroblast Growth FactorsLamininMaleMolecular Sequence DataSignal TransductionTranscriptional ActivationWound HealingZebrafishZebrafish ProteinsFibroblast Growth Factorslamb1a protein, zebrafishLamininZebrafish Proteins

Identifiers

PMID26305099
PMCPMC4549328
OpenAlexW1613551306

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.