Investigating the role of CDC42 in the antiinflammatory effects of statins

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dc.contributor.advisor McDowell, Susan A.
dc.contributor.author Luft, Marissa
dc.date.accessioned 2017-08-08T18:19:49Z
dc.date.available 2017-08-08T18:19:49Z
dc.date.issued 2017-05
dc.identifier.other A-384
dc.identifier.uri http://cardinalscholar.bsu.edu/handle/123456789/200969
dc.description.abstract Although inflammation is a primary means for fighting infection, improper regulation of inflammation can result in life threatening conditions. Statins, prescribed to lower cholesterol, also have anti-inflammatory properties. These effects are mediated in part due to decreased synthesis of isoprenoid intermediates that are required by multiple GTP-binding proteins to attach at cell membranes. This study establishes a method for investigating if inhibition of CDC42, a potential master regulator, is sufficient to mimic the anti-inflammatory properties of statins and thus revealing if CDC42 plays a central role in mediating the anti-inflammatory action of statins on macrophages. Macrophages are one of the first immune cells activated in the inflammatory pathway. Expression of macrophage inflammatory surface proteins is used as a measurement of inflammatory response. Here, we compare the expression of macrophage inflammatory surface proteins between untreated macrophages and macrophages treated with lovastatin or ML 141, a small molecule inhibitor that acts selectively on CDC42. en_US
dc.description.sponsorship Honors College
dc.subject.lcsh Biology.
dc.title Investigating the role of CDC42 in the antiinflammatory effects of statins en_US
dc.type Undergraduate senior honors thesis.
dc.description.degree Thesis (B.?) en_US
dc.identifier.cardcat-url http://liblink.bsu.edu/uhtbin/catkey/1854280


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  • Undergraduate Honors Theses [5263]
    Honors theses submitted to the Honors College by Ball State University undergraduate students in partial fulfillment of degree requirements.

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