Publication Date

2017

Document Type

Thesis

Committee Members

Ji Bihl (Committee Member), David Cool (Committee Member), Jeffrey Travers (Advisor)

Degree Name

Master of Science (MS)

Abstract

Microvesicle particles (MVP) are found to be important for cellular communication because they contain many bioactive proteins, lipids, cytokines, and nucleic acids. We have previously found that ultraviolet B radiation (UVB) and a Platelet-activating factor agonist (CPAF) can stimulate the release of MVP in keratinocytes. We hypothesized that there may also be an increase in MVP released after thermal burn and that could be involved in pathogenesis of the systemic effects found in some patients. In this thesis various keratinocyte cell lines, mice and human ex vivo skin were used as model systems to test our hypotheses. It was determined that thermal burn significantly increases the release of MVP compared to the untreated groups. UVB, CPAF and thermal burn all seemed to involve acid sphingomyelinase (aSMase), but different MAP kinase pathways. There was also a significant decrease in the cytokine concentration inside MVP after thermal burn, suggesting a possible defense mechanism to prevent cytokine storm.

Page Count

151

Department or Program

Department of Pharmacology and Toxicology

Year Degree Awarded

2017

Creative Commons License

Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License.


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