# Influence of micro- and nanoscale cues on immune factors secretion: implications for immunomodulation

**Authors:** Zhiling Luo, Yulian Zheng, Wentao Lin, Liang Zhang, Xinyi Huang, Yongli Li, Yushan He, Xiao Shen, Hengshu Zhang, Wei Huang, Wenguo Cui, Lu Chen

PMC · DOI: 10.1093/rb/rbaf130 · Regenerative Biomaterials · 2025-12-18

## TL;DR

This study shows that fiber size at the micro- and nanoscale can influence immune cell secretions, offering a new way to control inflammation and tissue repair.

## Contribution

The study identifies fiber diameter as a key physical cue for immunomodulation through activation of the FAK-Wnt pathway.

## Key findings

- Microscale fibers increased secretion of pro-regenerative factors like VEGF, EGF, IL-10, and TGF-β1.
- Microscale fibers reduced pro-inflammatory factors such as TNF-α and IL-6.
- In vivo, microscale fibers promoted neovascularization and accelerated tissue repair.

## Abstract

Immune factors secreted by immune cells play a pivotal role in orchestrating inflammatory responses and facilitating tissue regeneration. Fiber dressings, owing to their extracellular matrix-like architecture and tunable physical properties, have emerged as promising candidates in regenerative medicine. Beyond serving as passive structural supports, fibers are increasingly recognized as active modulators of cell behavior through their inherent physical characteristics. However, how fiber diameter at the micro- and nanoscale influences the immune factor secretion profile of immune cells remains poorly defined. In this study, three types of fibers with distinct diameter scales were fabricated to systematically assess their immunomodulatory effects. In vitro analyses revealed that microscale fibers markedly enhanced the secretion of pro-regenerative and anti-inflammatory factors, such as VEGF, EGF, IL-10 and TGF-β1, while suppressing pro-inflammatory factors including TNF-α and IL-6. Mechanistic investigations indicated that this size-dependent immunomodulation may be driven by activation of the FAK-Wnt signaling pathway triggered by topographical cues. In vivo, microscale fibers significantly promoted neovascularization, attenuated inflammatory responses and accelerated tissue repair, further corroborating their immunoregulatory potential in a physiological setting. These findings establish fiber diameter as a critical physical cue for shaping the immune microenvironment and present a new strategy for immunoregulation through structural design. This work provides a conceptual framework for the development of biomaterials with intrinsic immunomodulatory properties and offers new therapeutic insights for the treatment of chronic inflammation-associated disorders.

## Linked entities

- **Proteins:** VEGFA (vascular endothelial growth factor A), EGF (epidermal growth factor), IL10 (interleukin 10), TGFB1 (transforming growth factor beta 1), TNF (tumor necrosis factor), IL6 (interleukin 6), PTK2 (protein tyrosine kinase 2), Wnt (protein Wnt-2)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, PTK2 (protein tyrosine kinase 2) [NCBI Gene 5747] {aka FADK, FADK 1, FAK, FAK1, FRNK, PPP1R71}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}
- **Diseases:** chronic inflammation (MESH:D007249)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12867575/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12867575/full.md

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Source: https://tomesphere.com/paper/PMC12867575