William Sessa, PhD
Alfred Gilman Professor Emeritus of PharmacologyCards
About
Titles
Alfred Gilman Professor Emeritus of Pharmacology
Biography
Dr. William C. Sessa is the Alfred Gilman Professor and Vice Chairman in the Department of Pharmacology and Director of the Vascular Biology & Therapeutics Program at Yale School of Medicine. His work defined the molecular aspects and physiological implications of endothelial nitric oxide synthase (eNOS) activation and has contributed towards the elucidation of how nitric oxide (NO) regulates angiogenesis, vascular permeability, atherosclerosis and vascular remodeling. He cloned eNOS as a post-doc and subsequently identified eNOS subcellular trafficking, post-translational lipidation, phosphorylation and regulated protein-protein interactions as mechanisms to regulate NO production and cardiovascular homeostasis. In addition to work on eNOS, he has made several additional important contributions emanating from his work on eNOS including elucidating the role of caveolae microdomains of the plasma membrane in signaling, defining the role of Akt as an important kinase regulating the morphogenic and survival pathway for angiogenic growth factors, and the identification of the enzyme required for dolichol synthesis in mammalian cells. This latter pathway is an evolutionarily conserved pathway for all protein N-glycosylation reactions in the endoplasmic reticulum and loss of functions mutations arising in this enzyme can cause a congenital disorder of glycosylation, pediatric epilepsy and movement disorders. He has trained many graduate students, mentored several clinical scientists and over 40 post-doctoral fellows, most of which are in leadership positions in academia.
Appointments
Pharmacology
EmeritusPrimary
Other Departments & Organizations
Education & Training
- Post-doctoral fellow
- Pharmacology, The University of Virginia Health Sciences Center (1993)
- Post-doctoral fellow/Senior Scientist
- The William Harvey Research Institute (1991)
- PhD
- New York Medical College (1989)
Research
Overview
The vascular endothelium is the largest endocrine organ in the body, at the interface of blood and tissue. As such, many common diseases such as atherosclerosis, heart disease, cancer, macular degeneration and diabetes have a common signature of endothelial cell dysfunction. Our laboratory is focused on understanding the etiology of vascular dysfunction in these diseases and is focused on several broad aspects of endothelial cell biology and function.
We are exploring multiple avenues of research with a critical eye towards discovering new, biologically relevant therapeutic targets and pathways.
1. Elucidation how endothelial NOS (eNOS) is regulated in the context of normal physiology and in disease using cellular and molecular approaches in signal transduction. Particular areas are the study of cholesterol enriched plasmalemmal microdomains, caveolins, cavins, and downstream pathways.
2. Identification of new pathways that mediate the uptake and transcytosis of low density lipoprotein (LDL) and determining how LDL receptor influences vascular disease.
3. Proteomic analysis of protein phosphorylation using optogenetic approaches;
4 NgBR structure function and cellular biology in cholesterol metabolism and protein N-glycosylation;
We typically use basic molecular and cellular approaches and apply our findings to complex genetic systems (compound mutant mouse strains) to study blood vessel structure and function in physiology and disease.
Medical Research Interests
Academic Achievements & Community Involvement
News
News
- January 09, 2024
Recap & Reflections: Vascular Biology & Therapeutics Program & Cardiovascular Research Center 2023 Retreat
- March 13, 2019
North American Vascular Biology Organization Honors Eichmann and Sessa
- March 11, 2019Source: North American Vascular Biology Organization (NAVBO)
William Sessa selected as the 2019 recipient of the Earl P. Benditt Award
- February 13, 2017Source: Office of Cooperative Research
Finalists Named for the Blavatnik Fund Highlighting Promising Research Across Yale