Evidence map›Paper›PMID 29973273›Full record

ArticleSkeletal muscle2018

Klotho expression is a prerequisite for proper muscle stem cell function and regeneration of skeletal muscle.

Hellen E Ahrens, Judith Huettemeister, Manuel Schmidt, Christoph Kaether, Julia von Maltzahn

Open access · goldAbstract read
In one paragraph

Article in Skeletal muscle, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 19% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  9. Hyperphosphatemia Contributes to Skeletal Muscle Atrophy in Mice.International journal of molecular sciences · 2024
    Article
  10. Review
  11. Article
  12. Article
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  14. We need to talk-how muscle stem cells communicate.Frontiers in cell and developmental biology · 2024
    Review
  15. Article
  16. 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

5 authors at 2 institutions in 1 country.

Hellen E AhrensLeibniz-Institute on Aging - Fritz-Lipmann-Institute, Beutenbergstrasse 11, 07745, Jena, Germany.
Judith HuettemeisterLeibniz-Institute on Aging - Fritz-Lipmann-Institute, Beutenbergstrasse 11, 07745, Jena, Germany.
Manuel SchmidtLeibniz-Institute on Aging - Fritz-Lipmann-Institute, Beutenbergstrasse 11, 07745, Jena, Germany.
Christoph KaetherLeibniz-Institute on Aging - Fritz-Lipmann-Institute, Beutenbergstrasse 11, 07745, Jena, Germany.
Julia von MaltzahnLeibniz-Institute on Aging - Fritz-Lipmann-Institute, Beutenbergstrasse 11, 07745, Jena, Germany. julia.vonmaltzahn@leibniz-fli.de.ORCID 0000-0001-7674-1487
Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEMax Delbrück Center · DE

Funding

Deutsche Forschungsgemeinschaft MA-3975/2-1Leibniz-Gemeinschaft SAW2015
6 · The paper itself

Abstract

backgroundKlotho is a well-known anti-aging hormone, which serves as a suppressor of aging through a variety of mechanisms. Aging of skeletal muscle is concomitant with a decrease in muscle stem cell function resulting in impaired regeneration.

methodsHere we investigate the functional role of the anti-aging hormone Klotho for muscle stem cell function after cardiotoxin-induced injury of skeletal muscle using a klotho hypomorphic mouse line, which is characterized by a premature aging phenotype. Furthermore, we perform floating single myofiber cultures with their adjacent muscle stem cells to investigate the interplay between canonical Wnt signaling and Klotho function.

resultsWe demonstrate that muscle stem cell numbers are significantly decreased in klotho hypomorphic mice. Furthermore, we show that muscle stem cell function is also severely impaired upon loss of klotho expression, in culture and during regeneration in vivo. Moreover, we demonstrate that addition of recombinant Klotho protein inhibits aberrant excessive Wnt signaling in aged muscle stem cells thereby restoring their functionality.

conclusionsThe anti-aging hormone Klotho counteracts aberrant canonical Wnt signaling in muscle stem cells and might be one of the naturally occurring inhibitors of canonical Wnt signaling in skeletal muscle.

Indexed as

AgingAging, PrematureAnimalsCell DifferentiationCell ProliferationCells, CulturedGlucuronidaseKlotho ProteinsMice, Inbred C57BLMice, Mutant StrainsMuscle DevelopmentMuscle, SkeletalMyoblasts, SkeletalRegenerationRNA, MessengerWnt3A ProteinGlucuronidaseKlotho ProteinsRNA, MessengerWnt3A ProteinWnt3a protein, mouseAgingCanonical Wnt signaling, Wnt3aKlothoMuscle stem cellMyogenesisRegenerationSkeletal muscle

Identifiers

PMID29973273
PMCPMC6030782
OpenAlexW2810391611

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.