ML141 and its influence on endothelial cell and macrophage immune response

Cardinal Scholar

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dc.contributor.advisor McDowell, Susan A.
dc.contributor.author Hahn, Nathan
dc.date.accessioned 2019-09-27T18:59:27Z
dc.date.available 2019-09-27T18:59:27Z
dc.date.issued 2019-05-04
dc.identifier.uri http://cardinalscholar.bsu.edu/handle/123456789/201972
dc.description.abstract Staphylococcus aureus infections are a prevalent infection. Specific strains of S. aureus, such as MRSA (methicillin resistant Staphylococcus aureus), receive attention due to resistance to many first-line antibiotics, but this may only be part of the problem. Recurrent and persistent infections can be caused by S. aureus entering the bloodstream and migrating to secondary sites of infection. Establishment of these secondary sites of infection is caused in part by S. aureus invading host cells. Our lab previously demonstrated that ML141, a novel small molecule inhibitor with specificity for human protein CDC42, limited host cell invasion by S. aureus. Though CDC42-targeted therapeutics may present a way to limit intracellular S. aureus, inhibition of CDC42 may not be an obvious therapeutic option. CDC42 serves a wide variety of roles within human cells, including the regulation of the innate immune response. This work demonstrates that production of immune molecules in macrophage and endothelial cells is sustained in ML141 treated cells, suggesting short-term inhibition of CDC42 may provide a therapeutic approach to infection. en_US
dc.description.sponsorship Honors College
dc.subject.lcsh Biology.
dc.title ML141 and its influence on endothelial cell and macrophage immune response en_US
dc.type Undergraduate senior honors thesis
dc.description.degree Thesis (B.?) en_US


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  • Undergraduate Honors Theses [5772]
    Honors theses submitted to the Honors College by Ball State University undergraduate students in partial fulfillment of degree requirements.

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