Evidence map›Paper›PMID 27462298›Full record

ArticleFrontiers in endocrinology2016

Phosphatidylinositol 3-Kinase-Associated Protein (PI3KAP)/XB130 Crosslinks Actin Filaments through Its Actin Binding and Multimerization Properties In Vitro and Enhances Endocytosis in HEK293 Cells.

Daisuke Yamanaka, Takeshi Akama, Kazuhiro Chida, Shiro Minami, Koichi Ito, Fumihiko Hakuno, Shin-Ichiro Takahashi

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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 2 institutions in 1 country.

Daisuke YamanakaLaboratory of Cell Regulation, Department of Animal Resource Sciences, Graduate School of Agriculture and Life Science, The University of Tokyo, Bunkyo-ku, Japan; Laboratory of Food and Physiological Models, Department of Veterinary Medical Sciences, Graduate School of Agriculture and Life Science, The University of Tokyo, Kasama, Japan; Department of Bioregulation, Nippon Medical School, Kawasaki, Japan.
Takeshi AkamaLaboratory of Cell Regulation, Department of Animal Resource Sciences, Graduate School of Agriculture and Life Science, The University of Tokyo , Bunkyo-ku , Japan.
Kazuhiro ChidaLaboratory of Cell Regulation, Department of Animal Resource Sciences, Graduate School of Agriculture and Life Science, The University of Tokyo , Bunkyo-ku , Japan.
Shiro MinamiDepartment of Bioregulation, Nippon Medical School , Kawasaki , Japan.
Koichi ItoLaboratory of Food and Physiological Models, Department of Veterinary Medical Sciences, Graduate School of Agriculture and Life Science, The University of Tokyo , Kasama , Japan.
Fumihiko HakunoLaboratory of Cell Regulation, Department of Animal Resource Sciences, Graduate School of Agriculture and Life Science, The University of Tokyo , Bunkyo-ku , Japan.
Shin-Ichiro TakahashiLaboratory of Cell Regulation, Department of Animal Resource Sciences, Graduate School of Agriculture and Life Science, The University of Tokyo , Bunkyo-ku , Japan.
The University of Tokyo · JPNippon Medical School · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Actin-crosslinking proteins control actin filament networks and bundles and contribute to various cellular functions including regulation of cell migration, cell morphology, and endocytosis. Phosphatidylinositol 3-kinase-associated protein (PI3KAP)/XB130 has been reported to be localized to actin filaments (F-actin) and required for cell migration in thyroid carcinoma cells. Here, we show a role for PI3KAP/XB130 as an actin-crosslinking protein. First, we found that the carboxyl terminal region of PI3KAP/XB130 containing amino acid residues 830-840 was required and sufficient for localization to F-actin in NIH3T3 cells, and this region is directly bound to F-actin in vitro. Moreover, actin-crosslinking assay revealed that recombinant PI3KAP/XB130 crosslinked F-actin. In general, actin-crosslinking proteins often multimerize to assemble multiple actin-binding sites. We then investigated whether PI3KAP/XB130 could form a multimer. Blue native-PAGE analysis showed that recombinant PI3KAP/XB130 was detected at 250-1200 kDa although the molecular mass was approximately 125 kDa, suggesting that PI3KAP/XB130 formed multimers. Furthermore, we found that the amino terminal 40 amino acids were required for this multimerization by co-immunoprecipitation assay in HEK293T cells. Deletion mutants of PI3KAP/XB130 lacking the actin-binding region or the multimerizing region did not crosslink actin filaments, indicating that actin binding and multimerization of PI3KAP/XB130 were necessary to crosslink F-actin. Finally, we examined roles of PI3KAP/XB130 on endocytosis, an actin-related biological process. Overexpression of PI3KAP/XB130 enhanced dextran uptake in HEK 293 cells. However, most of the cells transfected with the deletion mutant lacking the actin-binding region incorporated dextran to a similar extent as control cells. Taken together, these results demonstrate that PI3KAP/XB130 crosslinks F-actin through both its actin-binding region and multimerizing region and plays an important role in endocytosis.

Indexed as

actinadaptor proteinendocytosisphosphatidylinositol 3-kinaseprotein self-assembly

Identifiers

PMID27462298
PMCPMC4939424
OpenAlexW2466532254

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.