Evidence map›Paper›PMID 35929607›Full record

ArticleeLife2022

Septin7 is indispensable for proper skeletal muscle architecture and function.

Mónika Gönczi, Zsolt Ráduly, László Szabó, János Fodor, Andrea Telek, Nóra Dobrosi, Norbert Balogh, Péter Szentesi, Gréta Kis, Miklós Antal and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. 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 15% 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, 23 citations in OpenAlex.

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  12. Reduced Expression of Septin7 Hinders Skeletal Muscle Regeneration.International journal of molecular sciences · 2023
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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 1 institution in 1 country.

Mónika GöncziDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-8421-4369
Zsolt RádulyDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
László SzabóDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
János FodorDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Andrea TelekDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Nóra DobrosiDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Norbert BaloghDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Péter SzentesiDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID 0000-0003-2621-2282
Gréta KisDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Miklós AntalDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-2457-7387
György TrencsenyiDivision of Nuclear Medicine and Translational Imaging, Department of Medical Imaging, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Beatrix DienesDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
László CsernochDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-2446-1456
University of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Today septins are considered as the fourth component of the cytoskeleton, with the Septin7 isoform playing a critical role in the formation of higher-order structures. While its importance has already been confirmed in several intracellular processes of different organs, very little is known about its role in skeletal muscle. Here, using Septin7 conditional knockdown (KD) mouse model, the C2C12 cell line, and enzymatically isolated adult muscle fibers, the organization and localization of septin filaments are revealed, and an ontogenesis-dependent expression of Septin7 is demonstrated. KD mice displayed a characteristic hunchback phenotype with skeletal deformities, reduction in in vivo and in vitro force generation, and disorganized mitochondrial networks. Furthermore, knockout of Septin7 in C2C12 cells resulted in complete loss of cell division while KD cells provided evidence that Septin7 is essential for proper myotube differentiation. These and the transient increase in Septin7 expression following muscle injury suggest that it may be involved in muscle regeneration and development.

Indexed as

Muscle Fibers, SkeletalMuscle, SkeletalAnimalsCell DifferentiationMiceMitochondriaSeptinsSept7 protein, mouseSeptinscell biologycytoskeletondevelopmenthumanmitochondriamouseregenerationseptinsskeletal muscle

Identifiers

PMID35929607
PMCPMC9355566
OpenAlexW4289886826

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.