Evidence map›Paper›PMID 30718399›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Inositol hexakisphosphate kinase 3 promotes focal adhesion turnover via interactions with dynein intermediate chain 2.

Tomas Rojas, Weiwei Cheng, Zhe Gao, Xiaoqi Liu, Yakun Wang, Adarsha P Malla, Alfred C Chin, Lewis H Romer, Solomon H Snyder, Chenglai Fu

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Review
  7. Article
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  9. Article
  10. The inositol pyrophosphate 5-InsPScience advances · 2020
    Article
  11. Review
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

10 authors at 2 institutions in 2 countries.

Tomas RojasSolomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Weiwei ChengDivision of Neuropathology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Zhe GaoDepartment of Physiology and Pathophysiology, Tianjin Medical University, 300070 Tianjin, China.
Xiaoqi LiuDepartment of Physiology and Pathophysiology, Tianjin Medical University, 300070 Tianjin, China.
Yakun WangDepartment of Physiology and Pathophysiology, Tianjin Medical University, 300070 Tianjin, China.
Adarsha P MallaSolomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Alfred C ChinSolomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Lewis H RomerDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University, Baltimore, MD 21287.
Solomon H SnyderSolomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205; ssnyder@jhmi.edu chenglaifu@tmu.edu.cn.
Chenglai FuDepartment of Physiology and Pathophysiology, Tianjin Medical University, 300070 Tianjin, China; ssnyder@jhmi.edu chenglaifu@tmu.edu.cn.ORCID 0000-0003-4300-9948
Johns Hopkins University · USTianjin Medical University · CN

Funding

NEUROCHEMICAL ACTIONS OF PSYCHOTROPIC DRUGSR37MH018501 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SNYDER, SOLOMON H. · 1990 to 2009
$11.5M
NEUROCHEMICAL ACTIONS OF PSYCHOTROPIC DRUGSR01MH018501 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SNYDER, SOLOMON H. · 1985 to 2019
$10.8M
NIMH NIH HHS R01 MH018501NIMH NIH HHS R37 MH018501
6 · The paper itself

Abstract

Cells express a family of three inositol hexakisphosphate kinases (IP6Ks). Although sharing the same enzymatic activity, individual IP6Ks mediate different cellular processes. Here we report that IP6K3 is enriched at the leading edge of migrating cells where it associates with dynein intermediate chain 2 (DIC2). Using immunofluorescence microscopy and total internal reflection fluorescence microscopy, we found that DIC2 and IP6K3 are recruited interdependently to the leading edge of migrating cells, where they function coordinately to enhance the turnover of focal adhesions. Deletion of IP6K3 causes defects in cell motility and neuronal dendritic growth, eventually leading to brain malformations. Our results reveal a mechanism whereby IP6K3 functions in coordination with DIC2 in a confined intracellular microenvironment to promote focal adhesion turnover.

Indexed as

BrainCell AdhesionCell MovementCellular MicroenvironmentCytoplasmic DyneinsDendritesFocal AdhesionsHEK293 CellsHumansNeuronsPhosphotransferases (Phosphate Group Acceptor)Cytoplasmic Dyneinsinositol hexakisphosphate kinasePhosphotransferases (Phosphate Group Acceptor)cell migrationdyneinFAKfocal adhesionIP6K

Identifiers

PMID30718399
PMCPMC6386689
OpenAlexW2914423902

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.