# Human Derived Exosome Injections (ASCE+ vs. CELLEXOSOME) Enhance Collagen Remodeling and Angiogenesis in Intact Skin: A Comparative Experimental Study

**Authors:** Noury Adel, Jack Kolenda, Francisco Llano, Jesper Thulesen, Francisco Hernandez Gomez Crespo, Yundun Shen, Youn Kyong Jo, Gabriela Yareli Zavala Resendiz, Diego Ivan Briseno Torres, Jesus Alejandro Lopez‐Lara, Ida Vega Thulesen

PMC · DOI: 10.1111/jocd.70787 · Journal of Cosmetic Dermatology · 2026-03-05

## TL;DR

This study compares two human-derived exosome treatments to see which is better at improving skin structure and blood vessel growth in healthy skin.

## Contribution

The study demonstrates that ASCE+ exosomes outperform Cell Exosome in promoting collagen and angiogenesis in intact skin.

## Key findings

- ASCE+ exosomes increased collagen density and microvascular counts more than Cell Exosome.
- Control and saline groups showed no significant changes in skin structure or vascular density.
- Exosome treatments induced collagen remodeling and angiogenesis in intact skin.

## Abstract

Exosomes derived from human cells have emerged as promising biological agents for enhancing skin quality through stimulation of collagen remodeling and angiogenesis. While their role in wound healing is well established, their effects on intact, non‐injured skin remain insufficiently investigated. Their biological activity depends on their molecular cargo, including growth factors, extracellular matrix‐modulating proteins, and angiogenic microRNAs.

To evaluate the impact of intradermal injection of two human‐derived exosome formulations on dermal architecture and vascular density in intact skin.

A total of 96 adult male Syrian golden hamsters were randomly assigned to four equal groups: untreated control, saline injection, Cell Exosome (0.1 mL), or ASCE+ Exosome (0.1 mL). Skin biopsies were collected at baseline, day 3, day 7, and day 14 post injection, with equal numbers of animals sacrificed per group and time point. Histological analyses (Hematoxylin & Eosin, Masson's Trichrome, Van Gieson) assessed dermal architecture and collagen organization, while CD34 immunohistochemistry quantified microvascular density. Quantitative image analysis was performed using ImageJ, with five high power fields evaluated per specimen. All assessments were performed in a blinded manner.

Untreated control and saline groups showed no significant histological or immunohistochemical changes across all time points, consistent with normal tissue architecture. Cell Exosome treatment produced moderate increases in collagen deposition and CD34 positive vessels. Quantitatively, ASCE+ increased collagen density and microvascular counts compared with Cell Exosome (p < 0.05), whereas control and saline groups showed no measurable changes.

Human derived exosomes promote collagen remodeling and angiogenesis in intact skin, with ASCE+ Exosome exhibiting superior efficacy over Cell Exosome. These findings highlight the potential of exosome‐based therapies as minimally invasive strategies for skin rejuvenation.

## Linked entities

- **Species:** Mesocricetus auratus (taxon 10036)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CD34 [NCBI Gene 101833962], CD34 (CD34 molecule) [NCBI Gene 947], MMRN1 (multimerin 1) [NCBI Gene 22915] {aka ECM, EMILIN4, GPIa*, MMRN}
- **Diseases:** infection (MESH:D007239), ulceration (MESH:D014456), weight loss (MESH:D015431), toxicity (MESH:D064420), inflammation (MESH:D007249), impaired mobility (MESH:D014086), necrosis (MESH:D009336), IACUC (MESH:D000820), allergy (MESH:D004342)
- **Chemicals:** xylazine (MESH:D014991), H&amp;E (MESH:D006371), saline (MESH:D012965), paraffin (MESH:D010232), ASCE (-), Hematoxylin (MESH:D006416), oxygen (MESH:D010100), DAB (MESH:C000469), Eosin (MESH:D004801), 3,3'-diaminobenzidine (MESH:D015100), formalin (MESH:D005557), citrate (MESH:D019343), lipids (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606], Cricetus cricetus (black-bellied hamster, species) [taxon 10034], Cricetinae (hamsters, subfamily) [taxon 10026], Mesocricetus auratus (golden hamster, species) [taxon 10036]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12963036/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963036/full.md

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Source: https://tomesphere.com/paper/PMC12963036