Evidence map›Paper›PMID 28794483›Full record

ArticleScientific reports2017

Impaired lymphocyte trafficking in mice deficient in the kinase activity of PKN1.

Rana Mashud, Akira Nomachi, Akihide Hayakawa, Koji Kubouchi, Sally Danno, Takako Hirata, Kazuhiko Matsuo, Takashi Nakayama, Ryosuke Satoh, Reiko Sugiura and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  4. Kinobead Profiling Reveals Reprogramming of BCR Signaling in Response to Therapy within Primary CLL Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
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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

16 authors at 7 institutions in 1 country.

Rana MashudGraduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.
Akira NomachiCenter for Innovation in Immunoregulative Technology and Therapeutics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Akihide HayakawaGraduate School of Science and Technology, Kobe University, Kobe, 657-8501, Japan.
Koji KubouchiGraduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.
Sally DannoGraduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.
Takako HirataDepartment of Fundamental Biosciences, Shiga University of Medical Science, Seta-Tsukinowa-cho Otsu, Shiga, 520-2192, Japan.
Kazuhiko MatsuoDivision of Chemotherapy, Kindai University School of Pharmacy, Kowakae, Higashi-Osaka, 577-8502, Japan.
Takashi NakayamaDivision of Chemotherapy, Kindai University School of Pharmacy, Kowakae, Higashi-Osaka, 577-8502, Japan.
Ryosuke SatohLaboratory of Molecular Pharmacogenomics, School of Pharmaceutical Sciences, Kindai University, 3-4-1, Kowakae, Higashi-Osaka, 577-8502, Japan.
Reiko SugiuraLaboratory of Molecular Pharmacogenomics, School of Pharmaceutical Sciences, Kindai University, 3-4-1, Kowakae, Higashi-Osaka, 577-8502, Japan.
Manabu AbeDepartment of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.
Kenji SakimuraDepartment of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.
Shigeharu WakanaJapan Mouse Clinic, RIKEN BioResource Center, 3-1-1 Koyadai, Tsukuba-shi, Ibaraki, 305-0074, Japan.ORCID 0000-0002-7037-8354
Hiroyuki OhsakiLaboratory of Pathology, Department of Medical Biophysics, Kobe University Graduate School of Health Sciences, 7-10-2 Tomogaoka, Suma, Kobe, Hyogo, 654-0142, Japan.
Shingo KamoshidaLaboratory of Pathology, Department of Medical Biophysics, Kobe University Graduate School of Health Sciences, 7-10-2 Tomogaoka, Suma, Kobe, Hyogo, 654-0142, Japan.
Hideyuki MukaiGraduate School of Medicine, Kobe University, Kobe, 650-0017, Japan. mukinase@kobe-u.ac.jp.
Kobe University · JPKindai University · JPNiigata University · JPKobe Pharmaceutical University · JPKyoto University · JPRIKEN BioResource Research Center · JPShiga University of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Knock-in mice lacking PKN1 kinase activity were generated by introducing a T778A point mutation in the catalytic domain. PKN1[T778A] mutant mice developed to adulthood without apparent external abnormalities, but exhibited lower T and B lymphocyte counts in the peripheral blood than those of wild-type (WT) mice. T and B cell development proceeded in an apparently normal fashion in bone marrow and thymus of PKN1[T778A] mice, however, the number of T and B cell counts were significantly higher in the lymph nodes and spleen of mutant mice in those of WT mice. After transfusion into WT recipients, EGFP-labelled PKN1[T778A] donor lymphocytes were significantly less abundant in the peripheral circulation and more abundant in the spleen and lymph nodes of recipient mice compared with EGFP-labelled WT donor lymphocytes, likely reflecting lymphocyte sequestration in the spleen and lymph nodes in a cell-autonomous fashion. PKN1[T778A] lymphocytes showed significantly lower chemotaxis towards chemokines and sphingosine 1-phosphate (S1P) than WT cells in vitro. The biggest migration defect was observed in response to S1P, which is essential for lymphocyte egress from secondary lymphoid organs. These results reveal a novel role of PKN1 in lymphocyte migration and localization.

Indexed as

AnimalsCell DifferentiationChemokinesChemotaxis, LeukocyteGenetic LociGenotypeImmunophenotypingLymphocyte ActivationLymphocyte CountLymphocytesLysophospholipidsMiceMice, TransgenicProtein Kinase CSphingosineChemokinesLysophospholipidsProtein Kinase Cprotein kinase NSphingosinesphingosine 1-phosphate

Identifiers

PMID28794483
PMCPMC5550459
OpenAlexW2743259091

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.