Date of Award
Spring 5-2002
Document Type
Thesis
Degree Name
Honors College
Department
Biology
First Advisor
Wesley Gray
Second Advisor
Joyce W. O'Rourke
Third Advisor
Beverly Wade
Abstract
Angiostatin is a proteolytic fragment of plasminogen that inhibits angiogenesis. It destroys newly formed capillaries and causes tumors to stop growing, shrink, or disappear altogether. We sought to determine if angiostatin could be produced from plasminogen by urokinase enzyme. We hypothesized that if angiostatin is produced, it could be an inhibitor of endothelial cell growth. To test this idea, plasminogen was purified by affinity chromatography using a sepharose-lysine column. Then, it was incubated with urokinase and 10% sodium azide. In order to produce angiostatin, samples were taken out at different time periods and analyzed on SDS-Page Gel electrophoresis gel designated to detect angiostatin. A Western Blot analysis prove that angiostatin was indeed present after plasminogen. We then examined angiostatin activity to determine if angiostatin inhibits endothelial cell growth. We demonstrated that angiostatin does indeed inhibit endothelial cell growth at the concentration produced [rom plasminogen. Thus our results showed that plasminogen can be converted to angiostatin by urokinase and angiostatin has shown inhibitory activity on endothelial cell proliferation.
Recommended Citation
Anderson, Jason C., "In vitro/in vivo activation of angiostatin" (2002). Electronic Dissertations and Theses. 15.
https://digitalcommons.subr.edu/dissertations_theses/15