A Small Molecule that Induces Intrinsic Pathway Apoptosis with Unparalleled Speed
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 Raptina...
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Veröffentlicht in: | Cell reports (Cambridge) 2015-12, Vol.13 (9), p.2027-2036 |
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Sprache: | eng |
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Zusammenfassung: | 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.
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•Discovery of a compound that induces unusually rapid apoptosis•Identification of specific mitochondrial processes critical to apoptotic induction
Palchaudhuri et al. describe the discovery of a small molecule called “Raptinal” that induces unusually rapid apoptotic cell death via the intrinsic pathway. Their work describes the utility of Raptinal as a tool for apoptosis induction relative to other available small molecules. |
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ISSN: | 2211-1247 2211-1247 |
DOI: | 10.1016/j.celrep.2015.10.042 |