David E. Cohen, M.D., Ph.D

Chief, Division of Gastroenterology & Hepatology
Vincent Astor Distinguished Professor of Medicine

Joan & Sanford I. Weill Department of Medicine
Weill Cornell Medical College


For almost two decades, Dr. Cohen’s research program has focused on understanding the molecular regulation of hepatic lipid and glucose metabolism.   Among his contributions has been to describe novel roles for phosphatidylcholine transfer protein (PC-TP) in the control of hepatic lipid and glucose homeostasis.  Because it binds phosphatidylcholines with high specificity and catalyzes their transfer between membranes in vitro, he originally proposed that PC-TP might play a role in the hepatocellular trafficking of biliary phospholipids to the canalicular membrane for secretion into bile and to the sinusoidal plasma membrane for incorporation into high density lipoprotein (HDL) particles.  In the course of these studies, he was the first to clone PC-TP, to characterize the gene and its transcription, and to express recombinant protein that we used to elucidate membrane-binding domains.  The Cohen laboratory crystallized PC-TP in complex with phosphatidylcholine, leading to our report of the three dimensional structure.  Studies in cell culture systems and Pctp-/- mice revealed much broader functions than anticipated in regulating metabolism.  In collaborative studies, Dr. Cohen utilized hyperinsulinemic euglycemic clamp studies to demonstrate that Pctp-/- mice are highly sensitized to insulin action and are protected against diet-induced diabetes due to suppression of hepatic glucose production.  His laboratory further showed that Pctp-/- mice exhibit increased adaptive thermogenesis due to increased sensitivity of brown adipocytes to stimulation by norepinephrine.  The Cohen Laboratory discovered small molecule inhibitors of PC-TP, which show promise for increasing insulin sensitivity in cells and in mice.  In separate studies, the laboratory demonstrated that PC-TP binds and activates thioesterase superfamily member (Them) 2, a newly described fatty acyl-CoA thioesterase.  We have also demonstrated key roles of both Them1 and Them2 in regulating hepatic lipid and glucose metabolism, as well as energy homeostasis.