Evidence map›Paper›PMID 12764139›Full record

ArticleThe Journal of biological chemistry2003

Calpain regulates enterocyte brush border actin assembly and pathogenic Escherichia coli-mediated effacement.

David A Potter, Anjaiah Srirangam, Kerry A Fiacco, Daniel Brocks, John Hawes, Carter Herndon, Masatoshi Maki, David Acheson, Ira M Herman

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  8. Effects of HIV protease inhibitor ritonavir on Akt-regulated cell proliferation in breast cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2006
    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

9 authors at 4 institutions in 2 countries.

David A PotterDivision of Hematology/Oncology, Walther Oncology Center and Veterans Affairs Medical Center and the Department of Biochemistry and Molecular Biology, Indiana University, Indianapolis, Indiana 46202, USA. dapotter@iupui.edu
Anjaiah Srirangam
Kerry A Fiacco
Daniel Brocks
John Hawes
Carter Herndon
Masatoshi Maki
David Acheson
Ira M Herman
Indiana University – Purdue University Indianapolis · USNagoya University · JPTufts University · USUniversity of Maryland, Baltimore · US

Funding

PILOT AND FEASIBILITY STUDIESP30DK034928 · NIDDK · TUFTS MEDICAL CENTER · PI PLAUT, ANDREW GEORGE · 1986 to 2007
$8.5M
Indiana Program of Excellence in Biomedical ComputingP20GM066402 · NIGMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI MCDONALD, CLEMENT J · 2002 to 2004
$1.0M
RETINAL MICROVASCULAR CELLS, MATRIX, &OCULAR DISORDERSR01EY009033 · NEI · TUFTS UNIVERSITY BOSTON · PI HERMAN, IRA M · 1993 to 2002
$817k
REGULATION OF ISOACTIN DYNAMICS IN LIVING CELLSR01GM055110 · NIGMS · TUFTS UNIVERSITY BOSTON · PI HERMAN, IRA M · 1997 to 2000
$288k
FUNCTIONAL ANALYSIS OF TRANSCRIPTION FACTORS IN HIV-1K08CA001562 · NCI · TUFTS MEDICAL CENTER · PI POTTER, DAVID ALEXANDER · 1991 to 1996
–
NCI NIH HHS K08 CA001562NEI NIH HHS EY09033NIDDK NIH HHS P30 DK034928NIDDK NIH HHS P30 DK34928NIGMS NIH HHS GM 55110NIGMS NIH HHS P20 GM066402NIGMS NIH HHS P20 GM66402
6 · The paper itself

Abstract

This study identifies calpain as being instrumental for brush border (BB) microvillus assembly during differentiation and effacement during bacterial pathogenesis. Calpain activity is decreased by 25-80% in Caco 2 lines stably overexpressing calpastatin, the physiological inhibitor of calpain, and the effect is proportional to the calpastatin/calpain ratio. These lines exhibit a 2.5-fold reduction in the rate of microvillus extension. Apical microvillus assembly is reduced by up to 50%, as measured by quantitative fluorometric microscopy (QFM) of ezrin, indicating that calpain recruits ezrin to BB microvilli. Calpain inhibitors ZLLYCHN2, MDL 28170, and PD 150606 block BB assembly and ezrin recruitment to the BB. The HIV protease inhibitor ritonavir, which inhibits calpain at clinically relevant concentrations, also blocks BB assembly, whereas cathepsin and proteasome inhibitors do not. Microvillus effacement is inhibited after exposure of calpastatin-overexpressing cells to enteropathogenic Escherichia coli. These results suggest that calpain regulates BB assembly as well as pathological effacement, and indicate that it is an important regulator involved in HIV protease inhibitor toxicity and host-microbial pathogen interactions.

Indexed as

ActinsCalcium-Binding ProteinsCalpainCell MembraneCytoplasmCytoskeletal ProteinsDown-RegulationEnterocytesEscherichia coliEzrinGenetic VectorsHumansMicroscopy, ConfocalMicroscopy, Electron, ScanningMicroscopy, FluorescenceMicrovilliActinsCalcium-Binding ProteinsCalpaincalpastatinCytoskeletal ProteinsEzrinPhosphoproteins

Identifiers

PMID12764139
PMCPMC2727654
OpenAlexW1966852463

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.