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An important role of ?-hemolysin in extracellular vesicles on the development of atopic dermatitis induced by Staphylococcus aureus.


ABSTRACT: Skin barrier disruption and dermal inflammation are key phenotypes of atopic dermatitis (AD). Staphylococcus aureus secretes extracellular vesicles (EVs), which are involved in AD pathogenesis. Here, we evaluated the role of EVs-associated ?-hemolysin derived from S. aureus in AD pathogenesis. ?-hemolysin production from S. aureus was detected using western blot analyses. The cytotoxic activity of ?-hemolysin on HaCaT keratinocytes was evaluated by measuring cell viability after treating cells with soluble and EVs-associated ?-hemolysin. To determine the type of cell death, HaCaT keratinocytes were stained with annexin V and 7-AAD. The in vivo effects of ?-hemolysin were evaluated by application of soluble and EV-associated ?-hemolysin on the mouse skin. The present study showed that increased ?-hemolysin was produced by S. aureus colonized on AD patients compared to healthy subjects. ?-hemolysin production was also related to AD severity. In addition, EV-associated ?-hemolysin was more cytotoxic to HaCaT keratinocytes than soluble ?-hemolysin, and ?-hemolysin-negative EVs did not induce keratinocyte death. EV-associated ?-hemolysin induced necrosis, but soluble ?-hemolysin induced apoptosis of keratinocytes. In vivo, skin barrier disruption and epidermal hyperplasia were induced by soluble and EV-associated ?-hemolysin. However, AD-like dermal inflammation was only caused by EV-associated ?-hemolysin. Moreover, neither skin barrier disruption nor AD-like skin inflammation was induced by ?-hemolysin-negative EVs. Taken together, ?-Hemolysin secreted from S. aureus, particularly the EV-associated form, induces both skin barrier disruption and AD-like skin inflammation, suggesting that EV-associated ?-hemolysin is a novel diagnostic and therapeutic target for the control of AD.

SUBMITTER: Hong SW 

PROVIDER: S-EPMC4084635 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

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An important role of α-hemolysin in extracellular vesicles on the development of atopic dermatitis induced by Staphylococcus aureus.

Hong Sung-Wook SW   Choi Eun-Byul EB   Min Taek-Ki TK   Kim Ji-Hyun JH   Kim Min-Hye MH   Jeon Seong Gyu SG   Lee Byung-Jae BJ   Gho Yong Song YS   Jee Young-Koo YK   Pyun Bok-Yang BY   Kim Yoon-Keun YK  

PloS one 20140703 7


Skin barrier disruption and dermal inflammation are key phenotypes of atopic dermatitis (AD). Staphylococcus aureus secretes extracellular vesicles (EVs), which are involved in AD pathogenesis. Here, we evaluated the role of EVs-associated α-hemolysin derived from S. aureus in AD pathogenesis. α-hemolysin production from S. aureus was detected using western blot analyses. The cytotoxic activity of α-hemolysin on HaCaT keratinocytes was evaluated by measuring cell viability after treating cells w  ...[more]

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