Evidence map›Paper›PMID 17601529›Full record

ArticleDevelopmental biology2007

Laminin alpha5 is necessary for submandibular gland epithelial morphogenesis and influences FGFR expression through beta1 integrin signaling.

Ivan T Rebustini, Vaishali N Patel, Julian S Stewart, Ann Layvey, Elisabeth Georges-Labouesse, Jeffrey H Miner, Matthew P Hoffman

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

61 citing papers in PubMed, 113 citations in OpenAlex.

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  18. A novel role for cilia-dependent sonic hedgehog signaling during submandibular gland development.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Article
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1 more citing papers are in PubMed but not listed here.

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 2 countries.

Ivan T RebustiniMatrix and Morphogenesis Unit, Laboratory of Cell and Developmental Biology, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892-4370, USA.
Vaishali N Patel
Julian S Stewart
Ann Layvey
Elisabeth Georges-Labouesse
Jeffrey H Miner
Matthew P Hoffman
National Institutes of Health · USCentre National de la Recherche Scientifique · FRNational Institute of Dental and Craniofacial Research · USWashington University in St. Louis · US

Funding

Growth Factor/Extracellular Matrix Interactions During Branching MorphogenesisZ01DE000707 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI HOFFMAN, MATTHEW P · 2004 to 2008
$1.8M
Intramural NIH HHS Z01 DE000707Intramural NIH HHS Z99 DE999999
6 · The paper itself

Abstract

Laminin alpha chains have unique spatiotemporal expression patterns during development and defining their function is necessary to understand the regulation of epithelial morphogenesis. We investigated the function of laminin alpha5 in mouse submandibular glands (SMGs). Lama5(-/-) SMGs have a striking phenotype: epithelial clefting is delayed, although proliferation occurs; there is decreased FGFR1b and FGFR2b, but no difference in Lama1 expression; later in development, epithelial cell organization and lumen formation are disrupted. In wild-type SMGs alpha5 and alpha1 are present in epithelial clefts but as branching begins alpha5 expression increases while alpha1 decreases. Lama5 siRNA decreased branching, p42 MAPK phosphorylation, and FGFR expression, and branching was rescued by FGF10. FGFR siRNA decreased Lama5 suggesting that FGFR signaling provides positive feedback for Lama5 expression. Anti-beta1 integrin antibodies decreased FGFR and Lama5 expression, suggesting that beta1 integrin signaling provides positive feedback for Lama5 and FGFR expression. Interestingly, the Itga3(-/-):Itga6(-/-) SMGs have a similar phenotype to Lama5(-/-). Our findings suggest that laminin alpha5 controls SMG epithelial morphogenesis through beta1 integrin signaling by regulating FGFR expression, which also reciprocally regulates the expression of Lama5. These data link changes in basement membrane composition during branching morphogenesis with FGFR expression and signaling.

Indexed as

AnimalsCell ProliferationEpitheliumFeedbackFibroblast Growth Factor 1Gene Expression Regulation, DevelopmentalGestational AgeIntegrin alpha3Integrin alpha6Integrin beta1LamininMiceMice, KnockoutModels, BiologicalMorphogenesisPhenotypeFgfr1 protein, mouseFgfr2 protein, mouseFibroblast Growth Factor 1Integrin alpha3Integrin alpha6Integrin beta1Lamininlaminin Alaminin alpha5Receptor, Fibroblast Growth Factor, Type 1Receptor, Fibroblast Growth Factor, Type 2Receptors, Fibroblast Growth FactorRNA, Small Interfering

Identifiers

PMID17601529
PMCPMC2097956
OpenAlexW2073007695

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.