Education: Education B.S. Biology, Northern Michigan University M.S. Molecular Biology, George Mason University Ph.D. Biochemistry, Catholic University of Louvain
Mulligan-Kehoe MJ, Wagner R, Wieland C, Powell R. A truncated plasminogen activator inhibitor-1 protein inhibits angiostatin (K1-3), a plasminogen cleavage product. J. Biol. Chem. 276(11):8588-8596, 2001. (view details on MedLine)
Mulligan-Kehoe MJ, Kleinman HK, Drinane M, Wieland C, Wagner RJ, Powell RJ A truncated plasminogen activator inhibitor-1 protein blocks the availability of heparin-binding VEGF-A isoforms. J. Biol. Chem. 277(50): 49077-49089, 2002 (view details on MedLine)
Drinane MC, Sherman JA, Hall AE, Simons M, Mulligan-Kehoe MJ. Plasminogen and plasmin activity in patients with coronary artery disease. J. Thromb. Haem. 4: 1288-1295, 2006. (view details on MedLine)
Drinane M, Walsh J, Mollmark J, Simons M, Mulligan-Kehoe MJ The anti-angiogenic activity of rPAI-1 23 inhibits fibroblast growth factor-2 functions. J. Biol. Chem. 281:33336-33344, 2006 (view details on MedLine)
Mulligan-Kehoe MJ, Drinane MC, Mollmark J, Casciola-Rosen L, Hummers LK, Hall A, Rosen A, Wiigley FM, Simons M Antiangiogenic plasma activity in patients with systemic sclerosis. Arthritis Rheum. 56: 3448-58, 2007 (view details on MedLine)
Drinane M, Mollmark J, Zagorchev L, Moodie K, Sun B, Hall A, Shipman S, Morganelli P, Simons M, Mulligan-Kehoe MJ The Antiangiogenic Activity of rPAI-123 Inhibits Vasa Vasorum and Growth of Atherosclerotic Plaque. Circ Res. 2009 Feb 13;104(3):337-45 (view details on MedLine)
Professional Interests:
The research focus in Dr. Mulligan-Kehoe’s laboratory is anti-angiogenesis. In vitro and ex vivo studies include:
- Identification of the signaling pathways that are activated in response to the activity of an anti-angiogenic recombinant truncated PAI-1 protein, rPAI-123, developed in Dr. Mulligan-Kehoe’s laboratory.
Investigating the mechanisms by which rPAI-123 inhibits angiogenesis associated with atherosclerotic plaque development in a mouse model of atherogenesis. Our current studies suggest that rPAI-123 promotes vessel regression accompanied by plaque regression.
-Development of systems for delivery of therapeutics to sites of neo-angiogenesis. This work will use endothelial precursor cells as vehicles for delivery of the anti-angiogenic rPAI-123 protein to sites of neo-angiogenesis in breast and brain tumors. These studies include microCT and microPET imaging of rPAI-123 inhibition of blood vessels that support tumor growth.
-Translational studies examine the anti-angiogenic factors found in plasma from scleroderma patients. Our recent findings show that these factors contribute to the vascular component of the disease.
Courses Taught:
PEMM 101-102
PEMM 275 (vascular biology)
Grant Information:
Current Funding
-Principal Investigator, R01 NIH/NHLBI
-Principal Investigator, Phillips Imaging Foundation Award
-Co-Investigator, SCCOR NIH/NHLBI