Apoptosis through Death Receptors in Temporal Lobe Epilepsy-Associated Hippocampal Sclerosis
Seizure models have demonstrated that neuroinflammation and neurodegeneration are preponderant characteristics of epilepsy. Considering the lack of clinical studies, our aim is to investigate the extrinsic pathway of apoptosis in pharmacoresistant temporal lobe epilepsy (TLE) associated with hippoca...
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| Format: | Article |
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Wiley
2016-01-01
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| Series: | Mediators of Inflammation |
| Online Access: | http://dx.doi.org/10.1155/2016/8290562 |
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| author | Marcelo Ananias Teocchi Lília D’Souza-Li |
| author_facet | Marcelo Ananias Teocchi Lília D’Souza-Li |
| author_sort | Marcelo Ananias Teocchi |
| collection | DOAJ |
| description | Seizure models have demonstrated that neuroinflammation and neurodegeneration are preponderant characteristics of epilepsy. Considering the lack of clinical studies, our aim is to investigate the extrinsic pathway of apoptosis in pharmacoresistant temporal lobe epilepsy (TLE) associated with hippocampal sclerosis (HS) patients, TLE(HS). By a specific death receptor-mediated apoptosis array plate, 31 upregulated targets were revealed in the sclerotic hippocampus from TLE(HS) patients. Amongst them are the encoding genes for ligands (FASLG, TNF, and TNFSF10) and death receptors (FAS, TNFRSF1A, TNFRSF10A, and TNFRSF10B). In addition, we evaluated the hippocampal relative mRNA expression of the two TNF receptors, TNFRSF1A and TNFRSF1B, in patients, being both upregulated (n=14; P<0.01 and P<0.04, resp.) when compared to the post mortem control group (n=4). Our results have clearly suggested that three different death receptor apoptotic systems may be associated with the maintenance and progression of TLE-associated HS: (1) TNF-TNFRSF1A, (2) FASLG-FAS, and (3) TNFSF10-TNFRSF10A/B. Their effects on epilepsy are still scarcely comprehended. Our study points out to TNF and TNF receptor superfamily pathways as important targets for pharmacological studies regarding the benefits of an anti-inflammatory therapy in these patients. |
| format | Article |
| id | doaj-art-3eecd85f4c504c83bd06c5e8bf1f532b |
| institution | Kabale University |
| issn | 0962-9351 1466-1861 |
| language | English |
| publishDate | 2016-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Mediators of Inflammation |
| spelling | doaj-art-3eecd85f4c504c83bd06c5e8bf1f532b2025-02-03T01:29:53ZengWileyMediators of Inflammation0962-93511466-18612016-01-01201610.1155/2016/82905628290562Apoptosis through Death Receptors in Temporal Lobe Epilepsy-Associated Hippocampal SclerosisMarcelo Ananias Teocchi0Lília D’Souza-Li1Centro de Investigação em Pediatria (CIPED), Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Rua Tessália Vieira de Camargo 126, Cidade Universitária “Zeferino Vaz”, 13083-887 Campinas, SP, BrazilCentro de Investigação em Pediatria (CIPED), Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Rua Tessália Vieira de Camargo 126, Cidade Universitária “Zeferino Vaz”, 13083-887 Campinas, SP, BrazilSeizure models have demonstrated that neuroinflammation and neurodegeneration are preponderant characteristics of epilepsy. Considering the lack of clinical studies, our aim is to investigate the extrinsic pathway of apoptosis in pharmacoresistant temporal lobe epilepsy (TLE) associated with hippocampal sclerosis (HS) patients, TLE(HS). By a specific death receptor-mediated apoptosis array plate, 31 upregulated targets were revealed in the sclerotic hippocampus from TLE(HS) patients. Amongst them are the encoding genes for ligands (FASLG, TNF, and TNFSF10) and death receptors (FAS, TNFRSF1A, TNFRSF10A, and TNFRSF10B). In addition, we evaluated the hippocampal relative mRNA expression of the two TNF receptors, TNFRSF1A and TNFRSF1B, in patients, being both upregulated (n=14; P<0.01 and P<0.04, resp.) when compared to the post mortem control group (n=4). Our results have clearly suggested that three different death receptor apoptotic systems may be associated with the maintenance and progression of TLE-associated HS: (1) TNF-TNFRSF1A, (2) FASLG-FAS, and (3) TNFSF10-TNFRSF10A/B. Their effects on epilepsy are still scarcely comprehended. Our study points out to TNF and TNF receptor superfamily pathways as important targets for pharmacological studies regarding the benefits of an anti-inflammatory therapy in these patients.http://dx.doi.org/10.1155/2016/8290562 |
| spellingShingle | Marcelo Ananias Teocchi Lília D’Souza-Li Apoptosis through Death Receptors in Temporal Lobe Epilepsy-Associated Hippocampal Sclerosis Mediators of Inflammation |
| title | Apoptosis through Death Receptors in Temporal Lobe Epilepsy-Associated Hippocampal Sclerosis |
| title_full | Apoptosis through Death Receptors in Temporal Lobe Epilepsy-Associated Hippocampal Sclerosis |
| title_fullStr | Apoptosis through Death Receptors in Temporal Lobe Epilepsy-Associated Hippocampal Sclerosis |
| title_full_unstemmed | Apoptosis through Death Receptors in Temporal Lobe Epilepsy-Associated Hippocampal Sclerosis |
| title_short | Apoptosis through Death Receptors in Temporal Lobe Epilepsy-Associated Hippocampal Sclerosis |
| title_sort | apoptosis through death receptors in temporal lobe epilepsy associated hippocampal sclerosis |
| url | http://dx.doi.org/10.1155/2016/8290562 |
| work_keys_str_mv | AT marceloananiasteocchi apoptosisthroughdeathreceptorsintemporallobeepilepsyassociatedhippocampalsclerosis AT liliadsouzali apoptosisthroughdeathreceptorsintemporallobeepilepsyassociatedhippocampalsclerosis |