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Gatsinzi, Tom
Publikationer (8 of 8) Visa alla publikationer
Gatsinzi, T. (2012). Regulation of apoptotic processes in neurodegeneration and cancer: In vitro studies on human neuroblastoma cells. (Doctoral dissertation). Stockholm: Department of Neurochemistry, Stockholm University
Öppna denna publikation i ny flik eller fönster >>Regulation of apoptotic processes in neurodegeneration and cancer: In vitro studies on human neuroblastoma cells
2012 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Apoptosis is a highly controlled process of cell death, which is vital for maintenance of all multicellular organisms. Aberrant regulation of apoptosis can give rise to pathological conditions such as neurodegenerative diseases and cancer. Here, we used different human neuroblastoma cell lines to study mechanisms that may be involved in either neurodegeneration or resistance to cancer treatment. First, we have designed and developed tau-anchored FRET sensors (tAFSs) for live cell imaging of local caspase activation. Using these sensors we showed that the Alzheimer’s disease related neurotoxic peptide, amyloid-β, induced a global activation of caspase-3 and -6, but not -9, in neuronally differentiated SH-SY5Y cells. We also investigated the possible role of NF-κB in the resistance to tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) in different human neuroblastoma cell lines. While N-type SH-SY5Y and IMR32 cells were unaffected, S-type SK-N-AS cells were clearly sensitized to TRAIL by different NF-κB inhibitory agents. However, no correlation between NF-κB inhibition and sensitization to TRAIL could be observed. Instead, induction of reactive oxygen species (ROS) seemed to play a more important role. Furthermore, using tAFSs we also showed that TRAIL resistance in SK-N-AS cells is mainly due to incomplete activation of caspase-3, and could be reversed by different PKC inhibitors.

Ort, förlag, år, upplaga, sidor
Stockholm: Department of Neurochemistry, Stockholm University, 2012. s. 71
Nationell ämneskategori
Biologiska vetenskaper Kemi
Forskningsämne
neurokemi med molekylär neurobiologi
Identifikatorer
urn:nbn:se:su:diva-79157 (URN)978-91-7447-553-1 (ISBN)
Disputation
2012-10-19, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16 B, Stockholm, 13:00 (Engelska)
Opponent
Handledare
Anmärkning

At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 2: Manuscript.

Tillgänglig från: 2012-09-27 Skapad: 2012-08-28 Senast uppdaterad: 2022-02-24Bibliografiskt granskad
Gatsinzi, T., Ivanova, E. V. & Iverfeldt, K. (2012). TRAIL resistance in human neuroblastoma SK-N-AS cells is dependent on protein kinase C and involves inhibition of caspase-3 proteolytic processing. Journal of Neuro-Oncology, 109(3), 503-512
Öppna denna publikation i ny flik eller fönster >>TRAIL resistance in human neuroblastoma SK-N-AS cells is dependent on protein kinase C and involves inhibition of caspase-3 proteolytic processing
2012 (Engelska)Ingår i: Journal of Neuro-Oncology, ISSN 0167-594X, E-ISSN 1573-7373, Vol. 109, nr 3, s. 503-512Artikel i tidskrift (Refereegranskat) 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.

Nyckelord
AFS, Caspases, Curcumin, Neuroblastoma, PKC, TRAIL
Nationell ämneskategori
Biologiska vetenskaper
Forskningsämne
neurokemi med molekylär neurobiologi
Identifikatorer
urn:nbn:se:su:diva-79146 (URN)10.1007/s11060-012-0932-2 (DOI)000308441700007 ()22798207 (PubMedID)
Forskningsfinansiär
Vetenskapsrådet
Tillgänglig från: 2012-08-28 Skapad: 2012-08-28 Senast uppdaterad: 2022-02-24Bibliografiskt granskad
Figueroa, R. A., Ramberg, V., Gatsinzi, T., Samuelsson, M., Zhang, M., Iverfeldt, K. & Hallberg, E. (2011). Anchored FRET sensors detect local caspase activation prior to neuronal degeneration. Molecular Neurodegeneration, 6, 35
Öppna denna publikation i ny flik eller fönster >>Anchored FRET sensors detect local caspase activation prior to neuronal degeneration
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2011 (Engelska)Ingår i: Molecular Neurodegeneration, E-ISSN 1750-1326, Vol. 6, s. 35-Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

BACKGROUND: Recent studies indicate local caspase activation in dendrites or axons during development and in neurodegenerative disorders such as Alzheimer's disease (AD). Emerging evidences point to soluble oligomeric amyloid-beta peptide as a causative agent in AD.

RESULTS: Here we describe the design of fluorescence resonance energy transfer (FRET)-based caspase sensors, fused to the microtubule associated protein tau. Specific caspase sensors preferentially cleaved by caspase-3, -6 or -9 were expressed in differentiated human neuroblastoma SH-SY5Y cells. The anchoring of the sensors resulted in high FRET signals both in extended neurites and soma and made analysis of spatiotemporal signal propagation possible. Caspase activation was detected as loss of FRET after exposure to different stimuli. Interestingly, after staurosporine treatment caspase-6 activation was significantly delayed in neurites compared to cell bodies. In addition, we show that exposure to oligomer-enriched amyloid-beta peptide resulted in loss of FRET in cells expressing sensors for caspase-3 and -6, but not -9, in both soma and neurites before neurite degeneration was observed.

CONCLUSIONS: Taken together, the results show that by using anchored FRET sensors it is possible to detect stimuli-dependent differential activation of caspases and to distinguish local from global caspase activation in live neuronal cells. Furthermore, in these cells oligomer-enriched amyloid-beta peptide induces a global, rather than local activation of caspase-3 and -6, which subsequently leads to neuronal cell death.

Nyckelord
Amyloid-beta, Caspases, FRET, Live Cell Imaging, Neurite degeneration, Neurodegeneration, Spatiotemporal analysis
Nationell ämneskategori
Biologiska vetenskaper Kemi
Forskningsämne
biokemi; neurokemi och neurotoxikologi; neurokemi med molekylär neurobiologi
Identifikatorer
urn:nbn:se:su:diva-58646 (URN)10.1186/1750-1326-6-35 (DOI)000291991900001 ()21605370 (PubMedID)
Forskningsfinansiär
Vetenskapsrådet, 2010-4481Vetenskapsrådet, 2010-4505
Tillgänglig från: 2011-06-07 Skapad: 2011-06-07 Senast uppdaterad: 2023-03-03Bibliografiskt granskad
Gatsinzi, T. & Iverfeldt, K. (2011). Sensitization to TRAIL-induced apoptosis in human neuroblastoma SK-N-AS cells by NF-kappa B inhibitors is dependent on reactive oxygen species (ROS). Journal of Neuro-Oncology, 104(2), 459-472
Öppna denna publikation i ny flik eller fönster >>Sensitization to TRAIL-induced apoptosis in human neuroblastoma SK-N-AS cells by NF-kappa B inhibitors is dependent on reactive oxygen species (ROS)
2011 (Engelska)Ingår i: Journal of Neuro-Oncology, ISSN 0167-594X, E-ISSN 1573-7373, Vol. 104, nr 2, s. 459-472Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) has been shown to induce apoptosis in a variety of cancer cell lines with almost no toxicity toward normal cells. However, many neuroblastoma cells acquire resistance to TRAIL by mechanisms that are poorly understood. The objective of this study was to investigate involvement of the transcription factor NF-kappa B in the resistance of human neuroblastoma SK-N-AS cells to TRAIL-induced apoptosis. We used five compounds previously reported to inhibit NF-kappa B activity. SN50, curcumin, oridonin, and pyrrolidine dithiocarbamate (PDTC) all sensitized cells to TRAIL-induced apoptosis. In contrast, N-alpha-tosyl-l-phenylalanyl chloromethyl ketone (TPCK) did not affect sensitivity to TRAIL, although reporter gene assay clearly showed inhibition of NF-kappa B activity. In addition, neither curcumin nor oridonin had any inhibitory effect on NF-kappa B activity at concentrations at which sensitization to TRAIL was observed. Instead, the free radical scavenger N-acetyl-l-cysteine (NAC) completely blocked the effect on TRAIL-induced apoptosis caused by curcumin, oridonin, and PDTC. Furthermore, exposure of SK-N-AS cells to H(2)O(2) could mimic the TRAIL-sensitizing effect of other agents. In conclusion, our results suggest that sensitization of neuroblastoma SK-N-AS cells to TRAIL-induced apoptosis is correlated with induction of reactive oxygen species (ROS) rather than inhibition of NF-kappa B.

Nyckelord
Apoptosis, Neuroblastoma, NF-kappa B, ROS, TRAIL
Nationell ämneskategori
Naturvetenskap
Identifikatorer
urn:nbn:se:su:diva-68003 (URN)10.1007/s11060-010-0516-y (DOI)000294263800006 ()
Anmärkning

authorCount :2

Tillgänglig från: 2012-01-03 Skapad: 2012-01-02 Senast uppdaterad: 2022-02-24Bibliografiskt granskad
Gatsinzi, T. (2009). Neuroblastoma cells: in vitro studies on childhood cancer and amyloid precursor protein processing enzymes. (Licentiate dissertation). Stockholm: Universitetsservice AB
Öppna denna publikation i ny flik eller fönster >>Neuroblastoma cells: in vitro studies on childhood cancer and amyloid precursor protein processing enzymes
2009 (Engelska)Licentiatavhandling, sammanläggning (Övrigt vetenskapligt)
Ort, förlag, år, upplaga, sidor
Stockholm: Universitetsservice AB, 2009. s. 54
Nationell ämneskategori
Naturvetenskap
Forskningsämne
neurokemi med molekylär neurobiologi
Identifikatorer
urn:nbn:se:su:diva-79162 (URN)ISBN 978-91-7155-848-0 (ISBN)
Presentation
2009-03-31, Heilbronnsalen, Svante Arrhenius väg 21A, 106 91 Stockholm, 16:50 (Engelska)
Opponent
Handledare
Tillgänglig från: 2012-10-30 Skapad: 2012-08-28 Senast uppdaterad: 2022-02-24Bibliografiskt granskad
Holback, S., Adlerz, L., Gatsinzi, T., Jacobsen, K. T. & Iverfeldt, K. (2008). PI3-K- and PKC-dependent up-regulation of APP processing enzymes by retinoic acid. Biochemical and Biophysical Research Communications - BBRC, 365(2), 298-303
Öppna denna publikation i ny flik eller fönster >>PI3-K- and PKC-dependent up-regulation of APP processing enzymes by retinoic acid
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2008 (Engelska)Ingår i: Biochemical and Biophysical Research Communications - BBRC, ISSN 0006-291X, E-ISSN 1090-2104, Vol. 365, nr 2, s. 298-303Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Retinoic acid stimulates α-secretase processing of amyloid precursor protein (APP) and decreases β-secretase cleavage that leads to amyloid-β formation. Here, we investigated the effect of retinoic acid on the two putative α-secretases, the disintegrin metalloproteinases ADAM10 and TACE, and the β-site cleaving enzyme BACE1, in human neuroblastoma SH-SY5Y cells. Western blot analysis showed that exposure to retinoic acid resulted in significantly increased levels of ADAM10 and TACE, suggesting that regulation of α-secretases causes the effects on APP processing. The presence of the phosphatidylinositol 3-kinase inhibitor LY 294002 selectively reduced the effect on ADAM10 protein levels but not on ADAM10 mRNA levels as determined by RT-PCR. On the other hand, the effect on TACE was shown to be dependent on protein kinase C, since it was completely blocked in the presence of the inhibitor bisindolylmaleimide XI. Our data indicate that different signalling pathways are involved in retinoic acid-induced up-regulation of the secretases.

Nyckelord
ADAM10, APP, BACE1, BDNF, PI3-kinase, Protein kinase C, Retinoic acid, TACE
Nationell ämneskategori
Naturvetenskap
Identifikatorer
urn:nbn:se:su:diva-19985 (URN)10.1016/j.bbrc.2007.10.167 (DOI)000251494000015 ()
Tillgänglig från: 2009-01-23 Skapad: 2009-01-23 Senast uppdaterad: 2022-02-25Bibliografiskt granskad
Gatsinzi, T., Jiang, Y., Langel, Ü. & Iverfeldt, K.Different strategies to inhibit NF-κB in order to sensitize Stypehuman neuroblastoma cells to TRAIL-induced apoptosis.
Öppna denna publikation i ny flik eller fönster >>Different strategies to inhibit NF-κB in order to sensitize Stypehuman neuroblastoma cells to TRAIL-induced apoptosis
(Engelska)Manuskript (preprint) (Övrigt vetenskapligt)
Nyckelord
Apoptosis, neuroblastoma, NF-κB, TRAIL
Nationell ämneskategori
Biokemi och molekylärbiologi
Forskningsämne
neurokemi med molekylär neurobiologi
Identifikatorer
urn:nbn:se:su:diva-79153 (URN)
Tillgänglig från: 2012-08-28 Skapad: 2012-08-28 Senast uppdaterad: 2022-02-24Bibliografiskt granskad
Ivanova, E. V., Gatsinzi, T., Figueroa, R. A., Hallberg, E. & Iverfeldt, K.Increased spatiotemporal resolution of caspase activation by anchoring FRET-based sensors to cytoskeleton.
Öppna denna publikation i ny flik eller fönster >>Increased spatiotemporal resolution of caspase activation by anchoring FRET-based sensors to cytoskeleton
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(Engelska)Manuskript (preprint) (Övrigt vetenskapligt)
Nyckelord
AFS, Apoptosis, Caspases, FRET, Live Cell Imaging
Nationell ämneskategori
Biologiska vetenskaper Kemi
Forskningsämne
neurokemi med molekylär neurobiologi
Identifikatorer
urn:nbn:se:su:diva-79138 (URN)
Forskningsfinansiär
Vetenskapsrådet
Tillgänglig från: 2012-08-28 Skapad: 2012-08-28 Senast uppdaterad: 2022-02-24Bibliografiskt granskad
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