Evidence map›Paper›PMID 31888027›Full record

ArticleInternational journal of molecular sciences2019

IRE1-XBP1 Pathway of the Unfolded Protein Response Is Required during Early Differentiation of C2C12 Myoblasts.

Yukako Tokutake, Keita Yamada, Satoko Hayashi, Wataru Arai, Takafumi Watanabe, Shinichi Yonekura

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Tumor necrosis factor α-induced endoplasmic reticulum stress promotes airway smooth muscle cell proliferation.American journal of physiology. Lung cellular and molecular physiology · 2026
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  2. Review
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  4. Molecular mechanisms underlying TNFα-induced mitochondrial fragmentation in human airway smooth muscle cells.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  5. 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

6 authors at 2 institutions in 1 country.

Yukako TokutakeDepartment of Bioscience and Food Production Science, Interdisciplinary Graduate School of Science and Technology, Shinshu University, Minamiminowa, Kamiina-gun, Nagano 399-4598, Japan.
Keita YamadaDepartment of Biomedical Engineering, Interdisciplinary Graduate School of Science and Technology, Shinshu University, Minamiminowa, Kamiina-gun, Nagano 399-4598, Japan.
Satoko HayashiDepartment of Biomedical Engineering, Interdisciplinary Graduate School of Science and Technology, Shinshu University, Minamiminowa, Kamiina-gun, Nagano 399-4598, Japan.
Wataru AraiDepartment of Biomedical Engineering, Interdisciplinary Graduate School of Science and Technology, Shinshu University, Minamiminowa, Kamiina-gun, Nagano 399-4598, Japan.
Takafumi WatanabeLaboratory of Anatomy, School of Veterinary Medicine, Rakuno Gakuen University, Ebetsu, Hokkaido 069-8501, Japan.
Shinichi YonekuraDepartment of Bioscience and Food Production Science, Interdisciplinary Graduate School of Science and Technology, Shinshu University, Minamiminowa, Kamiina-gun, Nagano 399-4598, Japan.
Shinshu University · JPRakuno Gakuen University · JP

Funding

Grant-in-Aid for JSPS Fellows 16J11238Grant-in-Aid for Scientific Research (C) 17K08042
6 · The paper itself

Abstract

In skeletal muscle, myoblast differentiation results in the formation of multinucleated myofibers. Although recent studies have shown that unfolded protein responses (UPRs) play an important role in intracellular remodeling and contribute to skeletal muscle differentiation, the involvement of IRE1-XBP1 signaling, a major UPR signaling pathway, remains unclear. This study aimed to investigate the effect of the IRE1-XBP1 pathway on skeletal muscle differentiation. In C2C12 cells, knockdown of IRE1 and XBP1 in cells remarkably suppressed differentiation. In addition, apoptosis and autophagy were dramatically enhanced in the XBP1-knockdown cells, highlighting the participation of IRE1-XBP1 in cell survival maintenance with differentiation stimuli during skeletal muscle differentiation. In myogenic cells, we demonstrated that the expression of CDK5 (cyclin-dependent kinase 5) is regulated by XBP1s, and we propose that XBP1 regulates the expression of MyoD family genes via the induction of CDK5. In conclusion, this study revealed that IRE1-XBP1 signaling plays critical roles in cell viability and the expression of differentiation-related genes in predifferentiated myoblasts and during the early differentiation phase.

Indexed as

AnimalsCell DifferentiationCell LineCell SurvivalCyclin-Dependent Kinase 5Gene Expression RegulationGene Knockdown TechniquesMembrane ProteinsMiceMyoblastsProtein Serine-Threonine KinasesSignal TransductionUnfolded Protein ResponseX-Box Binding Protein 1Cdk5 protein, mouseCyclin-Dependent Kinase 5Ern2 protein, mouseMembrane ProteinsProtein Serine-Threonine KinasesX-Box Binding Protein 1Xbp1 protein, mouseapoptosisautophagyskeletal muscle differentiationunfolded protein response (UPR)

Identifiers

PMID31888027
PMCPMC6981822
OpenAlexW2997180669

What OpenQuestion 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 OpenQuestion graph.