A Small Molecule that Induces Intrinsic Pathway Apoptosis with Unparalleled Speed.

Cell Rep
Authors
Keywords
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.

Year of Publication
2015
Journal
Cell Rep
Volume
13
Issue
9
Pages
2027-36
Date Published
2015 Dec 01
ISSN
2211-1247
URL
DOI
10.1016/j.celrep.2015.10.042
PubMed ID
26655912
PubMed Central ID
PMC4683402
Links
Grant list
1-T32-GM070421 / GM / NIGMS NIH HHS / United States
R01 CA120439 / CA / NCI NIH HHS / United States
T32 GM070421 / GM / NIGMS NIH HHS / United States
U54 NS079201 / NS / NINDS NIH HHS / United States
R01-CA120439 / CA / NCI NIH HHS / United States
NS079201 / NS / NINDS NIH HHS / United States