Evidence map›Paper›PMID 21678426›Full record

ArticleJournal of cellular physiology2012

Molecular characterization of myosin phosphatase in endothelium.

Kyung-Mi Kim, Csilla Csortos, Istvan Czikora, David Fulton, Nagavedi S Umapathy, Gabor Olah, Alexander D Verin

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-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

17 citing papers in PubMed, 29 citations in OpenAlex.

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  16. Ezrin/radixin/moesin proteins differentially regulate endothelial hyperpermeability after thrombin.American journal of physiology. Lung cellular and molecular physiology · 2013
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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

7 authors at 3 institutions in 2 countries.

Kyung-Mi KimVascular Biology Center, Georgia Health Sciences University, Augusta, Georgia 30912, USA.
Csilla Csortos
Istvan Czikora
David Fulton
Nagavedi S Umapathy
Gabor Olah
Alexander D Verin
Augusta University Health · USUniversity of Debrecen · HUThe University of Texas Medical Branch at Galveston · US

Funding

Microtubules in lung endothelial cell barrier regulationR01HL067307 · NHLBI · UNIVERSITY OF CHICAGO · PI VERIN, ALEXANDER D · 2001 to 2009
$2.5M
ATP in Lung Endothelial Barrier EnhancementR01HL083327 · NHLBI · UNIVERSITY OF CHICAGO · PI VERIN, ALEXANDER D · 2006 to 2009
$1.5M
ALK/SMAD Signaling in TGF beta-induced EC PermeabilityR01HL080675 · NHLBI · UNIVERSITY OF CHICAGO · PI VERIN, ALEXANDER D · 2005 to 2008
$1.5M
NHLBI NIH HHS HL 067307NHLBI NIH HHS HL083327NHLBI NIH HHS R01 HL067307NHLBI NIH HHS R01 HL080675NHLBI NIH HHS R01 HL083327
6 · The paper itself

Abstract

The phosphorylation status of myosin light chain (MLC) is regulated by both MLC kinases and type 1 Ser/Thr phosphatase (PPase 1), MLC phosphatase (MLCP) activities. The activity of the catalytic subunit of MLCP (CS1β) towards myosin depends on its associated regulatory subunit, namely myosin PPase targeting subunit 1 (MYPT1). Our previously published data strongly suggested the involvement of MLCP in endothelial cell (EC) barrier regulation. In this study, our new data demonstrate that inhibition of MLCP by either CS1β or MYPT1 siRNA-based depletion results in significant attenuation of purine nucleotide (ATP and adenosine)-induced EC barrier enhancement. Consistent with the data, thrombin-induced EC F-actin stress fiber formation and permeability increase were attenuated by the ectopic expression of constitutively active (C/A) MYPT1. The data demonstrated for the first time direct involvement of MLCP in EC barrier enhancement/protection. Cloning of MYPT1 in human pulmonary artery EC (HPAEC) revealed the presence of two MYPT1 isoforms, long and variant 2 (V2) lacking 56 amino acids from 553 to 609 of human MYPT1 long, which were previously identified in HeLa and HEK 293 cells. Our data demonstrated that in Cos-7 cells ectopically expressed EC MYPT1 isoforms co-immunoprecipitated with intact CS1β suggesting the importance of PPase 1 activity for the formation of functional complex of MYPT1/CS1β. Interestingly, MYPT1 V2 shows decreased binding affinity compared to MYPT1 long for radixin (novel MLCP substrate and a member of ERM family proteins). These results suggest functional difference between EC MYPT1 isoforms in the regulation of MLCP activity and cytoskeleton.

Indexed as

AnimalsBase SequenceCapillary PermeabilityCells, CulturedChlorocebus aethiopsCloning, MolecularCOS CellsCytoskeletal ProteinsDNA-Binding ProteinsEndothelial CellsHumansIsoenzymesMembrane ProteinsMyosin-Light-Chain PhosphataseProtein Interaction Domains and MotifsProtein SubunitsCytoskeletal ProteinsDNA-Binding ProteinsETV5 protein, humanIsoenzymesMembrane ProteinsMyosin-Light-Chain PhosphatasePPP1R12A protein, humanProtein SubunitsradixinRecombinant ProteinsRNA, Small InterferingTranscription Factors

Identifiers

PMID21678426
PMCPMC3695713
OpenAlexW2090361447

What OpenQuestion holds

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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.