Evidence map›Paper›PMID 40243453›Full record

ArticleInternational journal of molecular sciences2025

Myotube Formation and Cellular Fusion Are Diminished Due to Low Birth Weight in Piglets.

Katja Stange, Monika Röntgen

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Single nucleotide variations in theFrontiers in veterinary science · 2025
    Article
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

2 authors.

Katja StangeWorking Group Cell Biology of Muscle Growth, Research Institute for Farm Animal Biology (FBN), 18196 Dummerstorf, Germany.ORCID 0000-0002-8416-2204
Monika RöntgenWorking Group Cell Biology of Muscle Growth, Research Institute for Farm Animal Biology (FBN), 18196 Dummerstorf, Germany.ORCID 0000-0002-1159-4663

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low birth weight (LBW) in various species leads to a pronounced skeletal muscle phenotype and can serve as a model to study muscle formation and draw conclusions for normal and pathological development. We aimed to elucidate in detail how the differentiation of muscular stem cells and their progeny are disturbed in piglets born with LBW. We isolated primary muscle cells from LBW piglets and their normal siblings with two different approaches: (1) single cells from two functionally divergent subpopulations (previously named "fast" and "slow") and (2) cells derived from isolated, intact myofibers. Subsequently, we analyzed their proliferative and differentiative capacity by determining proliferation rate, migration behavior, myotube formation, and myogenic gene and protein expression. LBW led to a decreased proliferation rate and migration potential in cells from the subpopulation fast group. Cells from LBW piglets were generally able to differentiate, but they formed smaller myotubes with less incorporated nuclei, leading to a diminished fusion rate. Myogenic gene expression was also significantly altered due to pig birth weight. Overall, early postnatal muscle development in LBW was disturbed at several crucial steps involving the establishment of a reserve stem cell pool, movement of cells towards existing myofibers, and the ability to form nascent myofibers.

Indexed as

Birth WeightMuscle DevelopmentMuscle Fibers, SkeletalAnimalsAnimals, NewbornCell DifferentiationCell FusionCell MovementCell ProliferationCells, CulturedMuscle, SkeletalSwinelow birth weightmyofiber fusionmyogenic differentiation

Identifiers

PMID40243453
PMCPMC11989183

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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.