# Tumor-Derived Microvesicles Promote Kidney Regeneration and Cytoprotective Immunomodulation

**Authors:** Galina V. Seledtsova, Victor I. Seledtsov, Ayana B. Dorzhieva, Elena A. Blinova, Adas Darinskas, Elena A. Prokopyeva, Alexei A. von Delwig

PMC · DOI: 10.3390/ph18101520 · Pharmaceuticals · 2025-10-10

## TL;DR

Tumor-derived microvesicles can help repair damaged kidneys and reduce inflammation, similar to microvesicles from stem cells.

## Contribution

The study shows tumor-derived microvesicles can regenerate kidney tissue and modulate immune responses.

## Key findings

- Tumor-derived and stem cell-derived microvesicles improved kidney function and structure in a mouse model of chronic kidney injury.
- Both types of microvesicles reduced pro-inflammatory T cells and increased regulatory T cells in the spleen.
- Treatment restored normal levels of collecting tubules in the renal medulla.

## Abstract

Background: A comparative study was conducted to evaluate the potential of extracellular, tumor-derived microvesicles (MVs)s in promoting kidney regeneration. Methods: MVs were collected from L929 sarcoma, LLC, and B16 melanoma cells, and mesenchymal stem cells (MSCs). The regenerative activity of MVs was evaluated in an experimental murine model of chronic kidney injury (CKI). Results: Both tumor-derived MVs (T-MVs) and MSC-derived MVs (MSC-MVs) significantly improved kidney function and histological structure. Specifically, the height of collecting tubules in the middle third of the renal medulla returned to normal levels following MV treatment. Both T-MVs and MSC-MVs reduced the proportion of pro-inflammatory CD4+CD44+ T cells in renal cell infiltrates and spleens of CKI mice. Furthermore, treatment with these MVs increased the number of natural CD4+CD25+FoxP3+ regulatory T cells in the spleen, indicating their immunomodulatory effects. Conclusions: These findings suggest that T-MVs, similar to MSC-MVs, possess a universal capacity to promote kidney tissue regeneration and exert anti-inflammatory immunomodulatory effects.

## Linked entities

- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, Cd44 (CD44 antigen) [NCBI Gene 12505] {aka HERMES, Ly-24, Pgp-1}, Il2ra (interleukin 2 receptor, alpha chain) [NCBI Gene 16184] {aka CD25, Il2r, Ly-43}, Foxp3 (forkhead box P3) [NCBI Gene 20371] {aka JM2, scurfin, sf}
- **Diseases:** CKI (MESH:D051436), inflammatory (MESH:D007249), Tumor (MESH:D009369)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** B16 melanoma — Mus musculus (Mouse), Mouse melanoma, Cancer cell line (CVCL_F936), LLC — Mus musculus (Mouse), Malignant tumors of the mouse pulmonary system, Cancer cell line (CVCL_5653), L929 sarcoma — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_AR58)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12567108/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12567108/full.md

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Source: https://tomesphere.com/paper/PMC12567108