Evidence map›Paper›PMID 42681475›Full record

ArticleIn vitro cellular & developmental biology. Animal2026

Derivation and characterization of an embryonic‑derived muscle progenitor cell line from Atlantic salmon (Salmo salar).

Kyle Naylor, Sophia Webb, Deepika Rajesh, Patrick J Mee

Abstract read
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kyle NaylorRoslin Technologies Ltd, Roslin Innovation Centre, Easter Bush Campus, Edinburgh, EH25 9RG, UK.
Sophia WebbRoslin Technologies Ltd, Roslin Innovation Centre, Easter Bush Campus, Edinburgh, EH25 9RG, UK.
Deepika RajeshRoslin Technologies Ltd, Roslin Innovation Centre, Easter Bush Campus, Edinburgh, EH25 9RG, UK.
Patrick J MeeRoslin Technologies Ltd, Roslin Innovation Centre, Easter Bush Campus, Edinburgh, EH25 9RG, UK. joe.mee@roslintech.com.

Funding

Innovate UK 92260
6 · The paper itself

Abstract

Unlike mammals, teleost fish exhibit lifelong skeletal muscle growth, characterized by continued fiber hypertrophy and the formation of new muscle fibers maintained by a persistent progenitor cell population. However, the limited availability of stable muscle progenitor cell lines from commercially important species such as Atlantic salmon (Salmo salar) constrains mechanistic studies and emerging applications in cellular aquaculture. Here, we report the establishment and characterization of a novel embryonic-derived salmon muscle progenitor cell line, termed SsEC. These cells were derived from late embryonic stages and exhibited a spindle-shaped morphology, robust proliferative capacity, and sustained expansion beyond 30 passages under defined culture conditions. SsECs demonstrated a distinct extracellular matrix preference, with vitronectin supporting long-term maintenance and expansion. Molecular characterization confirmed stable expression of canonical myogenic markers, including myf5 and myod1, while transcriptomic profiling revealed enrichment of genes associated with muscle development and sarcomere organization relative to a non-myogenic salmon cell line. Directed differentiation to muscle, using a two-step protocol, induced efficient formation of multinucleated myotubes expressing myosin heavy chain and sarcomeric α-actinin, with upregulation of key differentiation markers such as myog and tnnt3a. Together, these findings establish SsECs as a robust in vitro model cell line for studying salmon muscle development and provide a novel platform for applications in aquaculture research and cellular seafood production.

Indexed as

Salmo salarStem CellsAnimalsCell DifferentiationCell LineCell ProliferationGene Expression ProfilingMuscle DevelopmentMuscle Fibers, SkeletalAquacultureAtlantic salmonCultivated seafoodEmbryonic-derivedEmbryonic progenitor cellsMuscle progenitorRNA-seqSalmo salarSkeletal myogenesis

Identifiers

PMID42681475
PMCPMC13582070

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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.