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Caspase activation in human neuroblastoma cells: mechanisms and spatiotemporal aspects
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för neurokemi.ORCID-id: 0000-0002-1007-747X
2015 (engelsk)Licentiatavhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Apoptosis is one of the modes of programmed cell death, in which several members of the caspase family of proteases play the central role. However, activation of apoptotic caspases does not necessarily lead to cell death. Instead, these caspases may mediate, for instance, differentiation or synaptic plasticity, if their activity is restricted in space and time. Such localized caspase activation has been also implicated in the initial stages of neurodegeneration. In order to assess this kind of events at a subcellular level, our research group has previously constructed tau-anchored FRET-based caspase sensors (tAFSs). Here, we demonstrate that localization of tAFSs to the cytoskeleton results in enrichment of the sensors in neuritic processes and enables increased spatiotemporal resolution for live cell imaging of caspase activation, as compared to soluble FRET sensors. This feature is particularly beneficial for investigation of neurodegeneration-related processes.

tAFSs were further employed for investigation of caspase activation in neuroblastoma, an extracranial solid pediatric tumor. Tumor necrosis factor-related apoptosis inducing factor (TRAIL) is a promising candidate for cancer treatment due to its ability to selectively trigger apoptosis malignant cells. However, many cancer cells, including neuroblastoma, acquire resistance to TRAIL. Here, we show that in S-type neuroblastoma cell lines, TRAIL resistance is dependent on incomplete activation of apoptotic caspase-3. Sensitization to TRAIL was achieved with protein kinase C (PKC)-inhibiting compounds, suggesting a role for this kinase in blocking the apoptotic response to TRAIL. This effect of PKC could possibly involve stabilization of XIAP, an endogenous caspase inhibitor, as PKC inhibition, in combination with TRAIL treatment, led to downregulation of XIAP.

sted, utgiver, år, opplag, sider
Stockholm: Department of Neurochemistry , 2015.
Emneord [en]
apoptosis, caspase, local caspase activation, neurodegeneration, tau-anchored FRET sensors, tAFS, cancer, neuroblastoma, TNF-related apoptosis inducing ligand, TRAIL, protein kinase C, PKC, X-linked inhibitor of apoptosis protein, XIAP
HSV kategori
Forskningsprogram
neurokemi med molekylär neurobiologi
Identifikatorer
URN: urn:nbn:se:su:diva-122651ISBN: 978-91-7649-303-8 (tryckt)OAI: oai:DiVA.org:su-122651DiVA, id: diva2:867633
Presentation
2015-11-27, Heilbronnsalen, C458, Svante Arrhenius väg 16B, Stockholm, 14:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2015-11-12 Laget: 2015-11-05 Sist oppdatert: 2015-11-12bibliografisk kontrollert
Delarbeid
1. Increased spatiotemporal resolution of caspase activation by anchoring FRET-based sensors to cytoskeleton
Åpne denne publikasjonen i ny fane eller vindu >>Increased spatiotemporal resolution of caspase activation by anchoring FRET-based sensors to cytoskeleton
Vise andre…
(engelsk)Manuskript (preprint) (Annet vitenskapelig)
Emneord
AFS, Apoptosis, Caspases, FRET, Live Cell Imaging
HSV kategori
Forskningsprogram
neurokemi med molekylär neurobiologi
Identifikatorer
urn:nbn:se:su:diva-79138 (URN)
Forskningsfinansiär
Swedish Research Council
Tilgjengelig fra: 2012-08-28 Laget: 2012-08-28 Sist oppdatert: 2016-01-29bibliografisk kontrollert
2. TRAIL resistance in human neuroblastoma SK-N-AS cells is dependent on protein kinase C and involves inhibition of caspase-3 proteolytic processing
Åpne denne publikasjonen i ny fane eller vindu >>TRAIL resistance in human neuroblastoma SK-N-AS cells is dependent on protein kinase C and involves inhibition of caspase-3 proteolytic processing
2012 (engelsk)Inngår i: Journal of Neuro-Oncology, ISSN 0167-594X, E-ISSN 1573-7373, Vol. 109, nr 3, s. 503-512Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Neuroblastoma is the most common solid extracranial cancer form in childhood with an etiology that is mostly unknown. Although tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) has been proposed as a promising future anticancer drug candidate, highly malignant neuroblastoma has been reported to acquire TRAIL resistance by mechanisms that are poorly understood. Here, we show by western blot analysis, and live cell imaging using anchored FRET sensors, that the resistance to TRAIL-induced apoptosis in human neuroblastoma SK-N-AS cells depends on an incomplete processing of procaspase-3, generating an immature and catalytically inactive 21 kDa fragment. We have previously shown that the naturally occurring compound curcumin can sensitize SK-N-AS cells to TRAIL. In the present study, we show that curcumin also has a similar effect on human neuroblastoma SHEP1 cells. Furthermore, we show that curcumin and TRAIL co-treatment induces complete maturation and activation of caspase-3 in both cell lines. The mechanisms behind this effect seem to be dependent on protein kinase C (PKC), since inhibition of PKC using bisindolylmaleimide XI, could also sensitize these cells to TRAIL through a similar effect on caspase-3 activation. Moreover, TRAIL co-treatment with bisindolylmaleimide XI or curcumin resulted in down-regulation of X-linked inhibitor of apoptosis protein. In conclusion, our study shows that PKC can be involved in TRAIL resistance in human neuroblastoma cells by preventing caspase-3 maturation.

Emneord
AFS, Caspases, Curcumin, Neuroblastoma, PKC, TRAIL
HSV kategori
Forskningsprogram
neurokemi med molekylär neurobiologi
Identifikatorer
urn:nbn:se:su:diva-79146 (URN)10.1007/s11060-012-0932-2 (DOI)000308441700007 ()22798207 (PubMedID)
Forskningsfinansiär
Swedish Research Council
Tilgjengelig fra: 2012-08-28 Laget: 2012-08-28 Sist oppdatert: 2018-09-12bibliografisk kontrollert

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