# MicroAge mission: experimental design and hardware for a bespoke culture system supporting tissue-engineered skeletal muscle

**Authors:** Samantha W. Jones, Shahjahan Shigdar, Jonathan Temple, Benjamin Tollitt, Adam Janvier, Fiona Mutter, James R. Henstock, Jessica Ohana, David A. Turner, Christopher McArdle, Gianluca Neri, William Blackler, Georgi Olentsenko, Kai. F. Hoettges, Anne McArdle, Malcolm J. Jackson

PMC · DOI: 10.1038/s41526-026-00579-z · NPJ Microgravity · 2026-02-21

## TL;DR

This paper describes a space mission using microgravity to study muscle aging and test genetic interventions to prevent muscle loss.

## Contribution

The study introduces a novel tissue-engineered skeletal muscle system for microgravity experiments and tests HSP10 overexpression as a potential countermeasure.

## Key findings

- Microgravity accelerates muscle atrophy similar to age-related decline on Earth.
- HSP10 overexpression shows potential to mitigate muscle atrophy in microgravity.
- A 3D-printed scaffold system was successfully developed for muscle construct experiments in space.

## Abstract

Microgravity provides a unique model for accelerated skeletal muscle loss and potentially muscle ageing. During spaceflight, astronauts experience pronounced muscle atrophy, similar to age-related decline on Earth but over a much shorter timescale. Despite daily aerobic and resistance exercise on the International Space Station (ISS), countermeasures remain suboptimal, reflecting similar challenges seen in ageing populations. The MicroAge Mission used microgravity on the ISS to assess whether the molecular mechanisms behind reduced adaptive responses to contractile activity during ageing resemble those triggered by spaceflight. It also tested proof-of-concept genetic interventions, including Heat Shock Protein 10 (HSP10) overexpression, to mitigate muscle atrophy and functional loss. A tissue-engineering approach was used to fabricate human skeletal muscle constructs secured to 3D-printed scaffolds. These scaffolds incorporated microfluidic channels to interface with the flight hardware’s fluid-handling system. The hardware, developed by Kayser Space Ltd, was designed to operate with the European Space Agency’s (ESA) Kubik incubator on the ISS. This research addresses key methodological constraints in low Earth orbit (LEO) experimentation, outlining pre-flight protocol development, muscle construct biofabrication methods, and operational considerations. The findings provide a translational framework for future studies on musculoskeletal degeneration, with implications for therapies targeting both terrestrial ageing and astronaut musculoskeletal health.

## Linked entities

- **Genes:** HSPE1 (heat shock protein family E (Hsp10) member 1) [NCBI Gene 3336]

## Full-text entities

- **Genes:** HSPE1 (heat shock protein family E (Hsp10) member 1) [NCBI Gene 3336] {aka CPN10, EPF, GROES, HSP10}
- **Diseases:** muscle atrophy (MESH:D009133), muscle loss (MESH:D009135), musculoskeletal degeneration (MESH:D009140)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13039470/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC13039470/full.md

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Source: https://tomesphere.com/paper/PMC13039470