Expert Details
Building Vascular Networks, Vascular Tumors, Endothelial Plasticity in Heart Valves
ID: 730062
Massachusetts, USA
Area I: Cellular and molecular basis of hemangioma – a vascular tumor of infancy and other types of vascular anomalies.
Hemangioma is a tumor of endothelial cells that occurs in infants. These tumors can grow rapidly, cause organ damage and disfigurement and even threaten life. Expert's laboratory is elucidating the cellular and molecular mechanisms that drive this uncontrolled growth. She has identified a hemangioma stem cell that forms all of the major cellular constituents of this vascular tumor – endothelial cells, pericytes and adipocytes. Her ultimate goal is to translate our basic research on hemangioma-derived stem cells and endothelial cells to develop safe fast-acting therapies that will stop hemangiomas from growing to a life-threatening or endangering size.
Area II: Using Blood-derived Endothelial Progenitors for Tissue Vascularization
Expert's goal is to build new vascular networks from human endothelial and mesenchymal progenitor cells to re-build damaged tissues and organs. She has shown that such cells can be obtained from human peripheral blood or bone marrow, expanded in the laboratory without difficulty, and used to build functional blood vessels in vivo in murine models. In the future, she envisions the use of a patient’s own endothelial and mesenchymal progenitor cells to build vascular networks for tissue-engineering applications and for in situ regeneration of vascular networks in ischemic tissue.
Area III: Plasticity of Cardiac Valvular Endothelium
Expert's laboratory has studied growth and differentiation of normal cardiac valvular endothelial cells for several years. Their studies have shown that valvular endothelial cells from adult valve cusps or leaflets can recapitulate processes that occur during valve development. These pathways involve transforming growth factor-ß and vascular endothelial growth factor (VEGF) signaling. Their recently published study indicates that the valvular endothelium harbors progenitor cells with endothelial/mesenchymal plasticity. They are studying this role of this inherent plasticity in the context of heart valve disease.
Education
Year | Degree | Subject | Institution |
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Year: 1985 | Degree: Ph.D. | Subject: biochemistry and molecular biology | Institution: Washington University School of Medicine |
Year: 1980 | Degree: A.B. | Subject: Chemistry | Institution: Duke University |
Work History
Years | Employer | Title | Department |
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Years: 1991 to Present | Employer: Undisclosed | Title: Undisclosed | Department: Surgery/Vascular Biology Program |
Responsibilities:She has directed her own independent and extra-murally funded research program since joining the faculty and the research staff at Employerin 1990. |
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Years | Employer | Title | Department |
Years: 1985 to 1990 | Employer: Undisclosed | Title: post-doctoral fellow | Department: Undisclosed |
Responsibilities:She was a post-doctoral fellow in the Harvey Lodish's laboratory, supported by a Helen Hay Whitney fellowship. |
Career Accomplishments
Associations / Societies |
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North American Vascular Biology Organization, International Society for the Study of Vascular Anomalies, American Society for Cell Biology |
Publications and Patents Summary |
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She has 78 peer-reviewed original research publications and 14 review articles and book chapters. She has two pending patent applications. |
Fields of Expertise
angiogenesis, blood vessel, endothelial cell biology, hemangioma, cavernous hemangioma, endothelium, endothelial cell, cell (biology), vascular endothelial cell growth factor, vascular anatomy, smooth muscle, capillary tube, vascular biology, biological cell differentiation, biological process, vascular disease, cardiovascular disease