After encounter with antigen in animals most activated T cells die rapidly. This event relieves the animal of the burden of excess lymphocytes and reduces the risk to the animal of autoimmunity and lymphoid tumors. The death of these cells is known to involve proteins related to Bcl-2, however, the way in which these proteins interact and cause the cells to die is not known. Likewise, anergic B cells also have a shortened half life and recent experiments that this phenomenon also involves members of the Bcl-2 family.Experiments in Project 3 will investigate these problems by studying the changes in amount of, andinteractions between, members of the Bcl-2 family of proteins as T cells convert from resting, long lived, toactivated, rapidly dying, cells and in anergic B cells. Many of the experiments will focus on Bim, a proteinwhich is very important in signaling lymphocytes to die, however, studies will also be performed to find outwhat substitutes for Bim when it is absent. In addition, viral analogs of the anti-apoptotic Bcl-2-like proteinswill be studied, since one of these proteins, though active in T cells, does not seem to be able to bind Bim inthe same way as Bcl-2 does. Moreover, these viral analogs act differently in T and B cells, thereforeexperiments on their action may reveal important differences between the ways T and B cells die. Finally, it is generally agreed that lymphocytes are actually killed by the Executioner proteins, Bak andBax. These proteins are thought to be triggered by other pro-apoptotic proteins such as Bim. However, themeans whereby Bim delivers the signal to kill to Bak and Bax is not known in spite of many years of study.This Project will follow up the idea that Bim triggers Bak and Bax via a 'hit and run' process, with mutationaland structural studies on the Executioners and Bim.
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