Evidence map›Paper›PMID 19325080›Full record

ArticleScience (New York, N.Y.)2009

Sequential regulation of DOCK2 dynamics by two phospholipids during neutrophil chemotaxis.

Akihiko Nishikimi, Hideo Fukuhara, Wenjuan Su, Tsunaki Hongu, Shunsuke Takasuga, Hisashi Mihara, Qinhong Cao, Fumiyuki Sanematsu, Motomu Kanai, Hiroshi Hasegawa and 6 more

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

146 citing papers in PubMed, 264 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  8. Membrane Ruffles: Composition, Function, Formation and Visualization.International journal of molecular sciences · 2024
    Review
  9. Article
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  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
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  18. Article
  19. DOCK4 Regulation of Rho GTPases Mediates Pulmonary Vascular Barrier Function.Arteriosclerosis, thrombosis, and vascular biology · 2022
    Article
  20. Article

86 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 2 countries.

Akihiko NishikimiDivision of Immunogenetics, Department of Immunobiology and Neuroscience, Medical Institute of Bioregulation, Kyushu University, Fukuoka 812-8582, Japan.
Hideo Fukuhara
Wenjuan Su
Tsunaki Hongu
Shunsuke Takasuga
Hisashi Mihara
Qinhong Cao
Fumiyuki Sanematsu
Motomu Kanai
Hiroshi Hasegawa
Yoshihiko Tanaka
Masakatsu Shibasaki
Yasunori Kanaho
Takehiko Sasaki
Michael A Frohman
Yoshinori Fukui
Japan Science and Technology Agency · JPKyushu University · JPUniversity of Tsukuba · JPAkita University · JPStony Brook University · US

Funding

Lipid-signaling pathways regulating mitochondrial morphology, energetics, and movR01GM084251 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI FROHMAN, MICHAEL A. · 2009 to 2017
$2.6M
Role of Phospholipase D1 in regulated exocytosisR01GM071520 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI FROHMAN, MICHAEL A. · 2006 to 2009
$1.3M
NIGMS NIH HHS R01 GM071520NIGMS NIH HHS R01 GM084251NIGMS NIH HHS R01GM71520
6 · The paper itself

Abstract

During chemotaxis, activation of the small guanosine triphosphatase Rac is spatially regulated to organize the extension of membrane protrusions in the direction of migration. In neutrophils, Rac activation is primarily mediated by DOCK2, an atypical guanine nucleotide exchange factor. Upon stimulation, we found that DOCK2 rapidly translocated to the plasma membrane in a phosphatidylinositol 3,4,5-trisphosphate-dependent manner. However, subsequent accumulation of DOCK2 at the leading edge required phospholipase D-mediated synthesis of phosphatidic acid, which stabilized DOCK2 there by means of interaction with a polybasic amino acid cluster, resulting in increased local actin polymerization. When this interaction was blocked, neutrophils failed to form leading edges properly and exhibited defects in chemotaxis. Thus, intracellular DOCK2 dynamics are sequentially regulated by distinct phospholipids to localize Rac activation during neutrophil chemotaxis.

Indexed as

Chemotaxis, Leukocyte1-ButanolActinsAnimalsCell LineCell MembraneCell PolarityEnzyme InhibitorsGTPase-Activating ProteinsGuanine Nucleotide Exchange FactorsHumansMiceNeutrophilsPhosphatidic AcidsPhosphatidylinositol PhosphatesPhospholipase D1-ButanolActinsDOCK2 protein, mouseEnzyme InhibitorsGTPase-Activating ProteinsGuanine Nucleotide Exchange FactorsPhosphatidic Acidsphosphatidylinositol 3,4,5-triphosphatePhosphatidylinositol PhosphatesPhospholipase Dphospholipase D2rac GTP-Binding ProteinsRecombinant Fusion Proteins

Identifiers

PMID19325080
PMCPMC3761877
OpenAlexW2024765629

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.