Evidence map›Paper›PMID 17785506›Full record

ArticleThe Journal of experimental medicine2007

Cdc42-interacting protein-4 functionally links actin and microtubule networks at the cytolytic NK cell immunological synapse.

Pinaki P Banerjee, Rahul Pandey, Rena Zheng, Megan M Suhoski, Linda Monaco-Shawver, Jordan S Orange

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

65 citing papers in PubMed, 102 citations in OpenAlex.

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  14. VASP Regulates NK Cell Lytic Granule Convergence.Journal of immunology (Baltimore, Md. : 1950) · 2018
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5 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

6 authors at 2 institutions in 1 country.

Pinaki P BanerjeeChildren's Hospital of Philadelphia, Division of Immunology, Abramson Research Center, Philadelphia, PA 19104, USA.
Rahul Pandey
Rena Zheng
Megan M Suhoski
Linda Monaco-Shawver
Jordan S Orange
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · US

Funding

Directing Function at the Natural Killer Cell Secretory Immunological SynapseR01AI067946 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ORANGE, JORDAN SCOTT · 2007 to 2019
$4.8M
Directing Function at the Natural Killer Cell Secretory Immunological SynapseR37AI067946 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Jordan Scott Orange · 2024 to 2026
$1.5M
Regulation of cytoskeletal activation in NK cellsK08AI055602 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI ORANGE, JORDAN SCOTT · 2003 to 2006
$483k
Directing Function at the Natural Killer Cell Secretory Immunological SynapseR56AI067946 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI ORANGE, JORDAN SCOTT · 2011 to 2011
$335k
NIAID NIH HHS AI055602NIAID NIH HHS AI067946NIAID NIH HHS K08 AI055602NIAID NIH HHS R01 AI067946NIAID NIH HHS R37 AI067946NIAID NIH HHS R56 AI067946
6 · The paper itself

Abstract

An essential function of the immunological synapse (IS) is directed secretion. NK cells are especially adept at this activity, as they direct lytic granules to the synapse for secretion, which enables cytotoxicity and facilitates host defense. This initially requires rearrangement of the actin cytoskeleton and, subsequently, microtubule-dependent trafficking of the lytic granules. As these two steps are sequential, specific linkages between them are likely to serve as critical regulators of cytotoxicity. We studied Cdc42-interacting protein-4 (CIP4), which constitutively interacts with tubulin and microtubules but focuses to the microtubule organizing center (MTOC) after NK cell activation, when it is able to associate with Wiskott-Aldrich syndrome protein (WASp) and the actin filament-rich IS. WASp deficiency, overexpression of CIP4, or parts of CIP4 interfere with this union and block normal CIP4 localization, MTOC polarization to the IS, and cytotoxicity. Reduction of endogenous CIP4 expression using small interfering RNA similarly inhibits MTOC polarization and cytotoxic activity but does not impair actin filament accumulation at the IS, or Cdc42 activation. Thus, CIP4 is an important cytoskeletal adaptor that functions after filamentous actin accumulation and Cdc42 activation to enable MTOC polarization and NK cell cytotoxicity.

Indexed as

Actinscdc42 GTP-Binding ProteinCell LineCell PolarityCell ShapeCytosolGene Expression RegulationHumansKiller Cells, NaturalMicrotubule-Associated ProteinsMicrotubule-Organizing CenterMicrotubulesMinor Histocompatibility AntigensProtein BindingWiskott-Aldrich Syndrome ProteinActinscdc42 GTP-Binding ProteinMicrotubule-Associated ProteinsMinor Histocompatibility AntigensTRIP10 protein, humanWiskott-Aldrich Syndrome Protein

Identifiers

PMID17785506
PMCPMC2118451
OpenAlexW2130251604

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.