Evidence map›Paper›PMID 23702582›Full record

ArticleThe Journal of investigative dermatology2013

β1 integrins with individually disrupted cytoplasmic NPxY motifs are embryonic lethal but partially active in the epidermis.

Alexander Meves, Christopher Stremmel, Ralph T Böttcher, Reinhard Fässler

Abstract read
In one paragraph

Article in The Journal of investigative dermatology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-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

14 citing papers in PubMed, 18 citations in OpenAlex.

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  11. Tumor Cell Adhesion As a Risk Factor for Sentinel Lymph Node Metastasis in Primary Cutaneous Melanoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2015
    Article
  12. Kindler syndrome in mice and men.Cancer biology & therapy · 2014
    Article
  13. Review
  14. 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 2 countries.

Alexander MevesDepartment of Dermatology, Mayo Clinic, Rochester, Minnesota, USA. Electronic address: meves.alexander@mayo.edu.
Christopher StremmelDepartment of Molecular Medicine, Max Planck Institute for Biochemistry, Martinsried, Germany.
Ralph T BöttcherDepartment of Molecular Medicine, Max Planck Institute for Biochemistry, Martinsried, Germany.
Reinhard FässlerDepartment of Molecular Medicine, Max Planck Institute for Biochemistry, Martinsried, Germany.
Max Planck Institute of Biochemistry · DEMayo Clinic · US

Funding

Montagna Symposium on the Biology of SkinR13AR009431 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI SANCY ANN LEACHMAN · 1986 to 2026
$785k
NIAMS NIH HHS R13 AR009431
6 · The paper itself

Abstract

β1 Integrin adhesion is believed to require binding of talins and kindlins to the membrane proximal and distal NPxY motifs of the β1 cytoplasmic tail, respectively. To test this hypothesis, we substituted the membrane proximal and distal tyrosines (Y) of the β1 tail with alanine (A) residues (β1 Y783A; β1 Y795A) in the germline of mice. We report that β1 Y783A or β1 Y795A substitutions blocked talin or kindlin binding, respectively, and led to β1 null-like peri-implantation lethality. Expression of β1 Y783A or β1 Y795A in the epidermis, however, resulted in skin blister and hair follicle phenotypes that were considerably milder than those observed with β1 integrin gene deletion or a β1 double Y-to-A substitution (β1 YY783/795AA). In culture, defects in adhesion, spreading, and migration were more severe with the β1 Y783A than with the β1 Y795A substitution despite markedly reduced β1 Y795A integrin surface levels owing to diminished protein stability. We conclude that regulation of β1 integrin adhesion through talins and kindlins may differ substantially between stably adherent keratinocytes and cells of the developing embryo, and that β1 cytoplasmic NPxY motifs contribute individually and independent of each other to β1 function in keratinocytes.

Indexed as

Gene Expression Regulation, DevelopmentalAmino Acid MotifsAnimalsCarrier ProteinsCell AdhesionCell MovementCytoplasmEmbryonic Stem CellsEpidermisGene DeletionHair FollicleIntegrin beta1Keratin-5KeratinocytesMicePhenotypeCarrier ProteinsIntegrin beta1Keratin-5kindlin-1 protein, mouseTalinTln1 protein, mouseTyrosine

Identifiers

PMID23702582
PMCPMC4535429
OpenAlexW2038333666

What OpenQuestion holds

Textmetadata
LicenceTDM
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.