Evidence map›Paper›PMID 21346190›Full record

ArticleMolecular biology of the cell2011

Direct binding of RalA to PKCη and its crucial role in morphological change during keratinocyte differentiation.

Yasuhito Shirai, Shoko Morioka, Megumi Sakuma, Ken-Ichi Yoshino, Chihiro Otsuji, Norio Sakai, Kaori Kashiwagi, Kazuhiro Chida, Ryutaro Shirakawa, Hisanori Horiuchi and 3 more

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In one paragraph

Article in Molecular biology of the cell, 2011. 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
0.4field-weighted citation impact, top 39% 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, 13 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

13 authors at 4 institutions in 1 country.

Yasuhito ShiraiLaboratory of Molecular Pharmacology, Biosignal Research Center, Kobe University, Kobe 657-8501, Japan. shirai@kobe-u.ac.jp
Shoko Morioka
Megumi Sakuma
Ken-Ichi Yoshino
Chihiro Otsuji
Norio Sakai
Kaori Kashiwagi
Kazuhiro Chida
Ryutaro Shirakawa
Hisanori Horiuchi
Chikako Nishigori
Takehiko Ueyama
Naoaki Saito
Kobe University · JPTohoku University · JPHiroshima University · JPTokyo University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During differentiation, keratinocytes undergo a dramatic shape change from small and round to large and flat, in addition to production of proteins necessary for the formation of epidermis. It has been shown that protein kinase C (PKC) η is crucial for keratinocyte differentiation. However, its role in this process has yet to be fully elucidated. Here, we show that catalytic activity is not necessary for enlarged and flattened morphology of human keratinocytes induced by overexpression of PKCη, although it is important for gene expression of the marker proteins. In addition, we identify the small G protein RalA as a binding partner of PKCη, which binds to the C1 domain, an indispensable region for the morphological change. The binding led activation of RalA and actin depolymerization associated with keratinocyte differentiation. siRNA techniques proved that RalA is involved in not only the keratinocyte differentiation induced by PKCη overexpression but also normal keratinocyte differentiation induced by calcium and cholesterol sulfate. These results provide a new insight into the molecular mechanism of cytoskeletal regulation leading to drastic change of cell shape.

Indexed as

Cell DifferentiationKeratinocytesActinsAdenoviridaeBinding SitesCalciumCell ShapeCholesterol EstersEnzyme ActivationEpidermal CellsEpidermisEscherichia coliGene ExpressionGene SilencingHEK293 CellsHumansActinsCalciumCholesterol Esterscholesteryl sulfateProtein Kinase Cprotein kinase C etaRALA protein, humanral GTP-Binding ProteinsRecombinant ProteinsRNA, Small Interfering

Identifiers

PMID21346190
PMCPMC3078077
OpenAlexW1987087186

What OpenQuestion holds

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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.