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June 26, 2025

Space-grown muscle tissues reveal rapid aging-like decline in microgravity

Green: Viability of live muscle tissue (Calcein AM staining, 4×). Red: Sarcomere striation formation within myotubes (α-Actinin staining, 20×). Blue: Muscle cell nuclei within myotubes (DAPI staining, 20×). Credit: Maddalena Parafati (Malany's Lab)
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Green: Viability of live muscle tissue (Calcein AM staining, 4×). Red: Sarcomere striation formation within myotubes (α-Actinin staining, 20×). Blue: Muscle cell nuclei within myotubes (DAPI staining, 20×). Credit: Maddalena Parafati (Malany's Lab)

Sarcopenia, which is a progressive and extensive decline in muscle mass and strength, is common with aging and is estimated to affect up to 50% of people aged 80 and older. It can lead to disability and injuries from falls and is associated with a lower quality of life and increased mortality. Apart from lifestyle changes, there is no current clinical treatment for sarcopenia.

Space flight with the associated absence of gravity and limited strain on muscles causes muscle weakness, a prominent feature of sarcopenia, within a short period of time, providing a time-lapse view on age-related atrophy-associated changes in the muscle. This relatively short window of time in space provides a microgravity model for muscular aging and opens opportunities for studying sarcopenia, which normally takes decades to develop in patients on Earth.

To understand the changes of muscle in microgravity, Siobhan Malany, Maddalena Parafati, and their team from the University of Florida, U.S., engineered skeletal muscle microtissues from donor biopsies and launched them to the International Space Station (ISS) aboard SpaceX CRS-25.

Their findings were in Stem Cell Reports.

The microtissues were taken from both young, active donors and from aged, sedentary donors and cultured in an automated mini-lab, which, besides regular feeding and monitoring of cultures, also enabled to simulate exercise.

On Earth, the contraction strength of microtissues from young, active individuals was almost twice as much as the strength of tissues from older, sedentary individuals.

After only two weeks in space, trended to decline in the young tissues and was now more comparable to the strength of old tissues. A similar trend was seen for the muscle protein content, which was higher in young microtissues on Earth compared to old microtissues but decreased in microgravity to levels measured in old tissues.

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Further, changed gene expression, particularly in the younger microtissues, and disturbed related to normal muscle function. Interestingly, electrical stimulation could mitigate these changes in to some extent.

"Using electrical pulses to trigger real-time muscle contractions in space, we can simulate exercise and observe how it helps protect against rapid muscle weakening in microgravity," said Siobhan Malany, one of the lead researchers.

"This technology advancement offers insight into how we might preserve muscle health during long-duration space missions and, ultimately, how to combat age-related muscle loss here on Earth."

This study shows that sarcopenia-related muscle decline can be modeled within a relatively short period in space and paves the way for follow-up studies on causes and potential treatments for sarcopenia from aging or space travel.

More information: Microgravity Accelerates Skeletal Muscle Degeneration: Functional and Transcriptomic Insights from an ISS Muscle Lab-on-Chip Model, Stem Cell Reports (2025). .

Journal information: Stem Cell Reports

Provided by International Society for Stem Cell Research

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Engineered human muscle tissues exposed to microgravity on the ISS exhibited rapid declines in strength and protein content, with young tissues deteriorating to levels similar to aged tissues within two weeks. Microgravity also altered gene expression and disrupted cellular processes, but electrical stimulation partially mitigated these effects, highlighting potential strategies to counteract muscle loss.

This summary was automatically generated using LLM.