# Aging Impairs Intramuscular Collagen Remodeling Responses to Repeated Passive Stretching in Skeletal Muscle

**Authors:** Yuji Kanazawa, Kenichiro Miyahara, Tatsuo Takahashi, Ryo Miyachi, Mamoru Nagano, Satoshi Koinuma, Naoya Iida, Takao Inoue, Yasufumi Shigeyoshi

PMC · DOI: 10.3390/ijms27062753 · 2026-03-18

## TL;DR

Aging reduces the ability of skeletal muscle collagen to adapt to stretching, affecting ECM stabilization processes.

## Contribution

The study reveals age-related impairments in collagen remodeling and ECM stabilization during passive stretching in skeletal muscle.

## Key findings

- Baseline gene expression of collagens I and IV was significantly reduced in aged muscles.
- Stretching increased collagen I immunoreactivity in both young and aged mice.
- Lysyl oxidase-positive cell changes were evident in young but not aged mice.

## Abstract

Aging is associated with changes in intramuscular collagen structure and metabolism, which may impair mechanical adaptability and regenerative capacity. We investigated the effects of aging and repeated passive stretching on intramuscular collagen remodeling in the tibialis anterior muscles of mice. The tibialis anterior muscles of young and aged mice were exposed to repeated passive stretching, and the localization of collagen and collagen-related factors was evaluated. Baseline gene expression of collagens I and IV was significantly reduced in aged muscles and was not restored by stretching. Repeated passive stretching increased the area and intensity of collagen I immunoreactivity in both young and aged mice but produced little change in collagen IV. Stretch-induced dynamic changes in lysyl oxidase-positive cells in the extracellular matrix (ECM) were evident in young mice but were markedly attenuated in aged mice. In addition, matrix metalloproteinases (MMP2 and MMP9) mRNA and protein expressions did not differ between groups. No significant age- or stretch-dependent changes were observed in the localization of advanced glycation end products. These findings suggest that although the increase in fibrillar collagen in response to stretching is maintained with aging, the regulatory mechanisms controlling ECM stabilization, particularly those related to cross-linking dynamics, may be impaired.

## Linked entities

- **Genes:** vkg (viking) [NCBI Gene 33726], MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313], MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Mmp2 (matrix metallopeptidase 2) [NCBI Gene 17390] {aka Clg4a, GelA, MMP-2}, Lox (lysyl oxidase) [NCBI Gene 16948] {aka TSC-160, rrg}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}
- **Chemicals:** advanced (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027270/full.md

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Source: https://tomesphere.com/paper/PMC13027270