REAL

Autophagy occurs upstream or parallel to the apoptosome during histolytic cell death

Akdemir, Fatih and Farkas, Robert and Chen, Po and Juhász, Gábor and Medved'ová, Lucia and Sass, Miklós and Wang, Lai and Wang, Xiaodong and Chittaranjan, Suganthi and Gorski, Sharon M. and Rodriguez, Antony and Abrams, John M. (2006) Autophagy occurs upstream or parallel to the apoptosome during histolytic cell death. Development, 133 (8). pp. 1457-1465. ISSN 0950-1991 (print), 1477-9129 (online)

[img]
Preview
PDF
1071531.pdf

Download (1MB)

Abstract

Histolysis refers to a widespread disintegration of tissues that is morphologically distinct from apoptosis and often associated with the stimulation of autophagy. Here, we establish that a component of the apoptosome, and pivotal regulator of apoptosis, is also required for histolytic cell death. Using in vivo and ex vivo assays, we demonstrate a global apoptogenic requirement for dark, the fly ortholog of Apaf1, and show that a required focus of dark– organismal lethality maps to the central nervous system. We further demonstrate that the Dark protein itself is a caspase substrate and find that alterations of this cleavage site produced the first hypermorphic point mutation within the Apaf1/Ced-4 gene family. In a model of ‘autophagic cell death’, dark was essential for histolysis but dispensable for characteristic features of the autophagic program, indicating that the induction of autophagy occurs upstream or parallel to histolytic cell death. These results demonstrate that stimulation of autophagy per se is not a ‘killing event’ and, at the same time, establish that common effector pathways, regulated by the apoptosome, can underlie morphologically distinct forms of programmed cell death.

Item Type: Article
Subjects: Q Science / természettudomány > QH Natural history / természetrajz > QH301 Biology / biológia
Depositing User: Erika Bilicsi
Date Deposited: 18 Dec 2012 07:25
Last Modified: 18 Dec 2012 07:25
URI: http://real.mtak.hu/id/eprint/3610

Actions (login required)

Edit Item Edit Item