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Updated: Jun 7, 2025

Author Spotlight: Accelerating Research on Bacterial Extracellular Vesicles Separation and Heterogeneity
Published on: September 1, 2023
Gut commensal bacteria Parabacteroides goldsteinii-derived outer membrane vesicles suppress skin inflammation in
Dandan Su1, Manchun Li1, Yuedong Xie1
1School of Pharmaceutical Sciences (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen 518107, China.
Abstract:
Despite gut microbiota-derived extracellular vesicles (EVs) serving as pivotal mediators in bacteria-host cell interactions, their potential role in modulating skin inflammation remains poorly understood. Here, we developed strategies for mass production of Parabacteroides goldsteinii-derived outer membrane vesicles (Pg OMVs), commonly known as EVs. We found that orally administered Pg OMVs can reach the colon, traverse the intestinal barrier, and circulate to the inflamed skin of psoriasis-like mice, resulting in reduced epidermal hyperplasia, suppressed infiltration of inflammatory cells in the skin lesions, and effective amelioration of both skin and systemic inflammation. Additionally, subcutaneous injection of thermosensitive PF-127 hydrogel loaded with Pg OMVs exerts similar immunomodulatory effects, allowing sustained release of Pg OMVs into skin cells, effectively suppressing skin inflammation and ameliorating symptoms of psoriasis. This study unveils the importance of gut microbiota-derived OMVs, which can target inflamed skin via both the gut-skin axis and local skin administration, providing a promising alternative to live bacteria therapy for the treatment of skin inflammatory diseases.
Insights
Gut bacteria outer membrane vesicles (OMVs) can travel from the gut to inflamed skin, reducing psoriasis-like symptoms. Local injection of these vesicles also effectively treats skin inflammation.
Area of Science:
- Microbiology
- Immunology
- Dermatology
Background:
- Gut microbiota-derived extracellular vesicles (EVs) are key in bacteria-host interactions.
- The role of EVs in modulating skin inflammation, particularly psoriasis, is largely unknown.
- Psoriasis involves complex immune dysregulation and skin inflammation.
Purpose of the Study:
- To investigate the therapeutic potential of Parabacteroides goldsteinii-derived outer membrane vesicles (Pg OMVs) for skin inflammation.
- To explore the gut-skin axis pathway for OMV delivery to inflamed skin.
- To evaluate local administration of Pg OMVs for sustained anti-inflammatory effects.
Main Methods:
- Mass production of Parabacteroides goldsteinii-derived outer membrane vesicles (Pg OMVs).
- Oral administration of Pg OMVs in psoriasis-like mouse models.
- Subcutaneous injection of Pg OMVs encapsulated in a thermosensitive hydrogel (PF-127).
Main Results:
- Orally administered Pg OMVs reached inflamed skin via the gut-skin axis.
- Pg OMVs treatment reduced epidermal hyperplasia and inflammatory cell infiltration in skin lesions.
- Both oral and local Pg OMV administration ameliorated skin and systemic inflammation in psoriasis-like mice.
Conclusions:
- Gut microbiota-derived OMVs can effectively target inflamed skin, offering a novel therapeutic strategy.
- Pg OMVs demonstrate significant immunomodulatory effects, reducing skin inflammation.
- This study presents OMVs as a promising alternative to live bacteria for treating inflammatory skin diseases.
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