Reference : 5-ALA-PDT induces RIP3-dependent necrosis in glioblastoma
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
http://hdl.handle.net/2268/101434
5-ALA-PDT induces RIP3-dependent necrosis in glioblastoma
English
Coupienne, Isabelle mailto [Université de Liège - ULg > > GIGA-R : Virologie - Immunologie >]
Fettweis, Grégory mailto [Université de Liège - ULg > > GIGA-R : Virologie - Immunologie >]
Rubio-Romero, Noemi mailto [Université de Liège - ULg > > GIGA-R : Virologie - Immunologie >]
Agostinis, Patrizia mailto [ > > ]
Piette, Jacques mailto [Université de Liège - ULg > Département des sciences de la vie > GIGA-R : Virologie - Immunologie >]
2011
Photochemical & Photobiological Sciences
Royal Society of Chemistry
Yes (verified by ORBi)
International
1474-905X
1474-9092
Cambridge
United Kingdom
[en] photodynamic therapy ; necrosis ; RIP3
[en] Glioblastoma constitute the most frequent and deadliest brain tumors of astrocytic origin. They are resistant to all current therapies and are associated with a high rate of recurrence. Glioblastoma were previously shown to respond to treatments by 5-aminolevulinic acid (5-ALA)-based photodynamic therapy (PDT) mainly by activating a necrotic type of cell death. The receptor-interacting protein 3 (RIP3) has recently been outlined as a key mediator of this caspase-independent form of programmed cell death. In the present study, we analyzed the necrotic mechanism induced by 5-ALA-PDT in human glioblastoma cells and explored the role of RIP3 in this context. Our results show that PDT-induced necrosis is dependent on RIP3, which forms aggregates and colocalizes with RIP1 following photosensitization. We demonstrate that PDT-mediated singlet oxygen production is the cause of RIP3-dependent necrotic pathway activation. We also prove that PDT induces the formation of a pro-necrotic complex containing RIP3 and RIP1 but lacking caspase-8 and FADD, two proteins usually part of the necrosome when TNF-α is used as a stimulus. Thus, we hypothesize that PDT might lead to the formation of a different necrosome whose components, besides RIP1 and RIP3, are still unknown. In most cases, glioblastoma are characterized by a constitutive activation of NF-κB. This factor is a key regulator of various processes, such as inflammation, immune response, cell growth or apoptosis. Its inhibition was shown to further sensitize glioblastoma cells to PDT-induced necrosis, however, no difference in RIP3 upshift or aggregation could be observed when NF-κB was inhibited.
Giga-Signal Transduction
Fonds pour la formation à la Recherche dans l'Industrie et dans l'Agriculture (Communauté française de Belgique) - FRIA ; Fonds de la Recherche Scientifique (Communauté française de Belgique) - F.R.S.-FNRS
http://hdl.handle.net/2268/101434
10.1039/c1pp05213f

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