| Literature DB >> 26655912 |
Rahul Palchaudhuri1, Michael J Lambrecht1, Rachel C Botham1, Kathryn C Partlow1, Tjakko J van Ham2, Karson S Putt3, Laurie T Nguyen3, Seok-Ho Kim1, Randall T Peterson2, Timothy M Fan4, Paul J Hergenrother5.
Abstract
Apoptosis is generally believed to be a process that requires several hours, in contrast to non-programmed forms of cell death that can occur in minutes. Our findings challenge the time-consuming nature of apoptosis as we describe the discovery and characterization of a small molecule, named Raptinal, which initiates intrinsic pathway caspase-dependent apoptosis within minutes in multiple cell lines. Comparison to a mechanistically diverse panel of apoptotic stimuli reveals that Raptinal-induced apoptosis proceeds with unparalleled speed. The rapid phenotype enabled identification of the critical roles of mitochondrial voltage-dependent anion channel function, mitochondrial membrane potential/coupled respiration, and mitochondrial complex I, III, and IV function for apoptosis induction. Use of Raptinal in whole organisms demonstrates its utility for studying apoptosis in vivo for a variety of applications. Overall, rapid inducers of apoptosis are powerful tools that will be used in a variety of settings to generate further insight into the apoptotic machinery.Entities:
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Year: 2015 PMID: 26655912 PMCID: PMC4683402 DOI: 10.1016/j.celrep.2015.10.042
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423