Evidence map›Paper›PMID 22306379›Full record

ArticleEuropean journal of cell biology2012

New isoform-specific monoclonal antibodies reveal different sub-cellular localisations for talin1 and talin2.

Uta Praekelt, Petra M Kopp, Kerstin Rehm, Stefan Linder, Neil Bate, Bipin Patel, Emmanuel Debrand, Ana Maria Manso, Robert S Ross, Franceso Conti and 5 more

Open access · greenAbstract read
In one paragraph

Article in European journal of cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

36 citing papers in PubMed, 69 citations in OpenAlex.

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  17. Integrin affinity modulation critically regulates atherogenic endothelial activation in vitro and in vivo.Matrix biology : journal of the International Society for Matrix Biology · 2021
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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

15 authors at 5 institutions in 3 countries.

Uta PraekeltDepartment of Biochemistry, University of Leicester, Lancaster Road, Leicester LE1 9HN, UK.
Petra M Kopp
Kerstin Rehm
Stefan Linder
Neil Bate
Bipin Patel
Emmanuel Debrand
Ana Maria Manso
Robert S Ross
Franceso Conti
Ming-Zhi Zhang
Raymond C Harris
Roy Zent
David R Critchley
Susan J Monkley
University of Leicester · GBVanderbilt University Medical Center · USUniversity Medical Center Hamburg-Eppendorf · DEUniversity of California, San Diego · USUniversity College London · GB

Funding

STRUCTUREU54GM064346 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI IMPERIALI, BARBARA · 2001 to 2010
$74.9M
Structure Function Analysis of Integrins alpha1beta1 and alpha2beta2R01DK083187 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SANDERS, CHARLES R, ZENT, ROY · 2010 to 2013
$1.3M
Cancer Research UKNIDDK NIH HHS R01 DK083187NIGMS NIH HHS U54 GM064346NIGMS NIH HHS U54 GM64346Wellcome Trust
6 · The paper itself

Abstract

Talins are adaptor proteins that connect the integrin family of cell adhesion receptors to cytoskeletal actin. Vertebrates express two closely related talins encoded by separate genes, and while it is well established that talin1 plays a key role in cell adhesion and spreading, little is known about the role of talin2. To facilitate such studies, we report the characterisation of 4 new isoform-specific talin mouse monoclonal antibodies that work in Western blotting, immuno-precipitation, immuno-fluorescence and immuno-histochemistry. Using these antibodies, we show that talin1 and talin2 do not form heterodimers, and that they are differentially localised within the cell. Talin1 was concentrated in peripheral focal adhesions while talin2 was observed in both focal and fibrillar adhesions, and knock-down of talin2 compromised fibronectin fibrillogenesis. Although differentiated human macrophages express both isoforms, only talin1 showed discrete staining and was localised to the ring structure of podosomes. However, siRNA-mediated knock-down of macrophage talin2 led to a significant reduction in podosomal matrix degradation. We have also used the antibodies to localise each isoform in tissue sections using both cryostat and paraffin-embedded material. In skeletal muscle talin2 was localised to both myotendinous junctions and costameres while talin1 was restricted to the former structure. In contrast, both isoforms co-localised in kidney with staining of the glomerulus, and the tubular epithelial and interstitial cells of the cortex and medulla. We anticipate that these antibodies will form a valuable resource for future studies on the function of the two major talin isoforms.

Indexed as

Antibodies, MonoclonalAnimalsAntibody SpecificityFibronectinsFocal AdhesionsGene Knockdown TechniquesHumansMacrophagesMiceMice, Inbred BALB CNIH 3T3 CellsProtein IsoformsRatsRNA, Small InterferingTalinAntibodies, MonoclonalFibronectinsProtein IsoformsRNA, Small InterferingTalinTln1 protein, mouseTLN2 protein, mouse

Identifiers

PMID22306379
PMCPMC3629562
OpenAlexW2037801641

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.