Abstract

Types of cell death include apoptosis, necrosis, and autophagic cell death. The latter can be defined as death of cells containing autophagosomes, autophagic bodies, and/or vacuoles. Are autophagy and vacuolization causes, consequences, or side effects in cell death with autophagy? Would control of autophagy suffice to control this type of cell death? We disrupted the atg1 autophagy gene in Dictyostelium discoideum, a genetically tractable model for developmental autophagic vacuolar cell death. The procedure that induced autophagy, vacuolization, and death in wild-type cells led in atg1 mutant cells to impaired autophagy and to no vacuolization, demonstrating that atg1 is required for vacuolization. Unexpectedly, however, cell death still took place, with a non-vacuolar and centrally condensed morphology. Thus, a cell death mechanism that does not require vacuolization can operate in this cell death model showing conspicuous vacuolization. The revelation of non-vacuolar cell death in this protist by autophagy gene disruption is reminiscent of caspase inhibition revealing necrotic cell death in animal cells. Thus, hidden alternative cell death pathways may be found across kingdoms and for diverse types of cell death.

Highlights

  • Three main forms of cell death have been described, caspasedependent apoptosis, and caspase-independent necrosis autophagic/vacuolar cell death

  • § Supported by an INSERM poste vert. ¶ Both authors contributed to this work. ʈ Supported by the European Community. ‡‡ To whom correspondence should be addressed: Centre d’Immunologie INSERM/CNRS/Universitede la Mediterranee, Case 906, Campus de Luminy, Ave. de Luminy, 13288 Marseille Cedex 9, France

  • A point at stake is whether control of autophagy in cells would help control some types of programmed cell death, for instance in pathological circumstances

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Summary

EXPERIMENTAL PROCEDURES

Cell Culture, and Microscopy—For cell death induction, unless stated otherwise Dictyostelium vegetative cells in growth phase were washed once and resuspended in HL5 medium at a concentration of 2 ϫ 105 cells/ml. One ml of this cell suspension was distributed in each well of Lab-Tek culture chambers (155380; Nalge Nunc, Naperville, IL). Atg Gene Inactivation by Homologous Recombination—The homologous recombination constructs for the deletion allele atg included 5Ј and 3Ј arms obtained separately by PCR from genomic DNA. Transformants were screened by PCR for homologous recombination of the insertion or deletion constructs with the endogenous atg locus.

RESULTS
SB plus DIF h
Incubation conditionsa SB SB plus DIF
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