Neuronal and astrocytic tetraploidy is increased in drug‐resistant epilepsy
Aims Epilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug‐resistant. The exact aetiology of drug‐resistant epilepsy (DRE) is still unknown. Neuronal tetraploidy has been associated with neuropathology. The aim of this study was to assess the pres...
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Published in | Neuropathology and applied neurobiology Vol. 49; no. 1; pp. e12873 - n/a |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
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01.02.2023
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ISSN | 0305-1846 1365-2990 1365-2990 |
DOI | 10.1111/nan.12873 |
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Abstract | Aims
Epilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug‐resistant. The exact aetiology of drug‐resistant epilepsy (DRE) is still unknown. Neuronal tetraploidy has been associated with neuropathology. The aim of this study was to assess the presence of tetraploid neurons and astrocytes in DRE.
Methods
For that purpose, cortex, hippocampus and amygdala samples were obtained from patients subjected to surgical resection of the epileptogenic zone. Post‐mortem brain tissue of subjects without previous records of neurological, neurodegenerative or psychiatric diseases was used as control.
Results
The percentage of tetraploid cells was measured by immunostaining of neurons (NeuN) or astrocytes (S100β) followed by flow cytometry analysis. The results were confirmed by image cytometry (ImageStream X Amnis System Cytometer) and with an alternative astrocyte biomarker (NDRG2). Statistical comparison was performed using univariate tests. A total of 22 patients and 10 controls were included. Tetraploid neurons and astrocytes were found both in healthy individuals and DRE patients in the three brain areas analysed: cortex, hippocampus and amygdala. DRE patients presented a higher number of tetraploid neurons (p = 0.020) and astrocytes (p = 0.002) in the hippocampus than controls. These results were validated by image cytometry.
Conclusions
We demonstrated the presence of both tetraploid neurons and astrocytes in healthy subjects as well as increased levels of both cell populations in DRE patients. Herein, we describe for the first time the presence of tetraploid astrocytes in healthy subjects. Furthermore, these results provide new insights into epilepsy, opening new avenues for future treatment.
We demonstrated the existence of tetraploid astrocytes in healthy human brain. Neural tetraploidy is increased in drug resistant epilepsy patients hippocampus. Astrocytic tetraploidy is higher in drug resistant epilepsy patients hippocampus. |
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AbstractList | Epilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug-resistant. The exact aetiology of drug-resistant epilepsy (DRE) is still unknown. Neuronal tetraploidy has been associated with neuropathology. The aim of this study was to assess the presence of tetraploid neurons and astrocytes in DRE.AIMSEpilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug-resistant. The exact aetiology of drug-resistant epilepsy (DRE) is still unknown. Neuronal tetraploidy has been associated with neuropathology. The aim of this study was to assess the presence of tetraploid neurons and astrocytes in DRE.For that purpose, cortex, hippocampus and amygdala samples were obtained from patients subjected to surgical resection of the epileptogenic zone. Post-mortem brain tissue of subjects without previous records of neurological, neurodegenerative or psychiatric diseases was used as control.METHODSFor that purpose, cortex, hippocampus and amygdala samples were obtained from patients subjected to surgical resection of the epileptogenic zone. Post-mortem brain tissue of subjects without previous records of neurological, neurodegenerative or psychiatric diseases was used as control.The percentage of tetraploid cells was measured by immunostaining of neurons (NeuN) or astrocytes (S100β) followed by flow cytometry analysis. The results were confirmed by image cytometry (ImageStream X Amnis System Cytometer) and with an alternative astrocyte biomarker (NDRG2). Statistical comparison was performed using univariate tests. A total of 22 patients and 10 controls were included. Tetraploid neurons and astrocytes were found both in healthy individuals and DRE patients in the three brain areas analysed: cortex, hippocampus and amygdala. DRE patients presented a higher number of tetraploid neurons (p = 0.020) and astrocytes (p = 0.002) in the hippocampus than controls. These results were validated by image cytometry.RESULTSThe percentage of tetraploid cells was measured by immunostaining of neurons (NeuN) or astrocytes (S100β) followed by flow cytometry analysis. The results were confirmed by image cytometry (ImageStream X Amnis System Cytometer) and with an alternative astrocyte biomarker (NDRG2). Statistical comparison was performed using univariate tests. A total of 22 patients and 10 controls were included. Tetraploid neurons and astrocytes were found both in healthy individuals and DRE patients in the three brain areas analysed: cortex, hippocampus and amygdala. DRE patients presented a higher number of tetraploid neurons (p = 0.020) and astrocytes (p = 0.002) in the hippocampus than controls. These results were validated by image cytometry.We demonstrated the presence of both tetraploid neurons and astrocytes in healthy subjects as well as increased levels of both cell populations in DRE patients. Herein, we describe for the first time the presence of tetraploid astrocytes in healthy subjects. Furthermore, these results provide new insights into epilepsy, opening new avenues for future treatment.CONCLUSIONSWe demonstrated the presence of both tetraploid neurons and astrocytes in healthy subjects as well as increased levels of both cell populations in DRE patients. Herein, we describe for the first time the presence of tetraploid astrocytes in healthy subjects. Furthermore, these results provide new insights into epilepsy, opening new avenues for future treatment. Aims Epilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug‐resistant. The exact aetiology of drug‐resistant epilepsy (DRE) is still unknown. Neuronal tetraploidy has been associated with neuropathology. The aim of this study was to assess the presence of tetraploid neurons and astrocytes in DRE. Methods For that purpose, cortex, hippocampus and amygdala samples were obtained from patients subjected to surgical resection of the epileptogenic zone. Post‐mortem brain tissue of subjects without previous records of neurological, neurodegenerative or psychiatric diseases was used as control. Results The percentage of tetraploid cells was measured by immunostaining of neurons (NeuN) or astrocytes (S100β) followed by flow cytometry analysis. The results were confirmed by image cytometry (ImageStream X Amnis System Cytometer) and with an alternative astrocyte biomarker (NDRG2). Statistical comparison was performed using univariate tests. A total of 22 patients and 10 controls were included. Tetraploid neurons and astrocytes were found both in healthy individuals and DRE patients in the three brain areas analysed: cortex, hippocampus and amygdala. DRE patients presented a higher number of tetraploid neurons (p = 0.020) and astrocytes (p = 0.002) in the hippocampus than controls. These results were validated by image cytometry. Conclusions We demonstrated the presence of both tetraploid neurons and astrocytes in healthy subjects as well as increased levels of both cell populations in DRE patients. Herein, we describe for the first time the presence of tetraploid astrocytes in healthy subjects. Furthermore, these results provide new insights into epilepsy, opening new avenues for future treatment. We demonstrated the existence of tetraploid astrocytes in healthy human brain. Neural tetraploidy is increased in drug resistant epilepsy patients hippocampus. Astrocytic tetraploidy is higher in drug resistant epilepsy patients hippocampus. AimsEpilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug‐resistant. The exact aetiology of drug‐resistant epilepsy (DRE) is still unknown. Neuronal tetraploidy has been associated with neuropathology. The aim of this study was to assess the presence of tetraploid neurons and astrocytes in DRE.MethodsFor that purpose, cortex, hippocampus and amygdala samples were obtained from patients subjected to surgical resection of the epileptogenic zone. Post‐mortem brain tissue of subjects without previous records of neurological, neurodegenerative or psychiatric diseases was used as control.ResultsThe percentage of tetraploid cells was measured by immunostaining of neurons (NeuN) or astrocytes (S100β) followed by flow cytometry analysis. The results were confirmed by image cytometry (ImageStream X Amnis System Cytometer) and with an alternative astrocyte biomarker (NDRG2). Statistical comparison was performed using univariate tests. A total of 22 patients and 10 controls were included. Tetraploid neurons and astrocytes were found both in healthy individuals and DRE patients in the three brain areas analysed: cortex, hippocampus and amygdala. DRE patients presented a higher number of tetraploid neurons (p = 0.020) and astrocytes (p = 0.002) in the hippocampus than controls. These results were validated by image cytometry.ConclusionsWe demonstrated the presence of both tetraploid neurons and astrocytes in healthy subjects as well as increased levels of both cell populations in DRE patients. Herein, we describe for the first time the presence of tetraploid astrocytes in healthy subjects. Furthermore, these results provide new insights into epilepsy, opening new avenues for future treatment. Epilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug-resistant. The exact aetiology of drug-resistant epilepsy (DRE) is still unknown. Neuronal tetraploidy has been associated with neuropathology. The aim of this study was to assess the presence of tetraploid neurons and astrocytes in DRE. For that purpose, cortex, hippocampus and amygdala samples were obtained from patients subjected to surgical resection of the epileptogenic zone. Post-mortem brain tissue of subjects without previous records of neurological, neurodegenerative or psychiatric diseases was used as control. The percentage of tetraploid cells was measured by immunostaining of neurons (NeuN) or astrocytes (S100β) followed by flow cytometry analysis. The results were confirmed by image cytometry (ImageStream X Amnis System Cytometer) and with an alternative astrocyte biomarker (NDRG2). Statistical comparison was performed using univariate tests. A total of 22 patients and 10 controls were included. Tetraploid neurons and astrocytes were found both in healthy individuals and DRE patients in the three brain areas analysed: cortex, hippocampus and amygdala. DRE patients presented a higher number of tetraploid neurons (p = 0.020) and astrocytes (p = 0.002) in the hippocampus than controls. These results were validated by image cytometry. We demonstrated the presence of both tetraploid neurons and astrocytes in healthy subjects as well as increased levels of both cell populations in DRE patients. Herein, we describe for the first time the presence of tetraploid astrocytes in healthy subjects. Furthermore, these results provide new insights into epilepsy, opening new avenues for future treatment. |
Author | Toledo, María Pereboom‐Maicas, Matilde Desirée Granero‐Cremades, Inmaculada Frade, José María Ovejero‐Benito, María C. Pulido, Paloma Navas, Marta Torres‐Díaz, Cristina Virginia Sanz‐García, Ancor Sánchez‐Jiménez, Patricia |
Author_xml | – sequence: 1 givenname: Ancor surname: Sanz‐García fullname: Sanz‐García, Ancor organization: Hospital Universitario de la Princesa, Instituto de Investigación Sanitaria La Princesa (IIS‐IP) – sequence: 2 givenname: Patricia surname: Sánchez‐Jiménez fullname: Sánchez‐Jiménez, Patricia organization: NIMGenetics Genómica y Medicina S.L – sequence: 3 givenname: Inmaculada surname: Granero‐Cremades fullname: Granero‐Cremades, Inmaculada organization: Hospital Universitario de La Princesa – sequence: 4 givenname: María orcidid: 0000-0003-0447-3422 surname: Toledo fullname: Toledo, María organization: Hospital Universitario de La Princesa – sequence: 5 givenname: Paloma surname: Pulido fullname: Pulido, Paloma organization: Hospital Universitario de La Princesa – sequence: 6 givenname: Marta surname: Navas fullname: Navas, Marta organization: Hospital Universitario de La Princesa – sequence: 7 givenname: José María surname: Frade fullname: Frade, José María organization: Instituto Cajal, CSIC – sequence: 8 givenname: Matilde Desirée surname: Pereboom‐Maicas fullname: Pereboom‐Maicas, Matilde Desirée organization: University of Zaragoza – sequence: 9 givenname: Cristina Virginia surname: Torres‐Díaz fullname: Torres‐Díaz, Cristina Virginia organization: Hospital Universitario de La Princesa – sequence: 10 givenname: María C. orcidid: 0000-0003-4082-5165 surname: Ovejero‐Benito fullname: Ovejero‐Benito, María C. email: maria.ovejerobenito@ceu.es organization: Universidad San Pablo‐CEU, CEU Universities |
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Keywords | temporal lobe epilepsy polyploidy refractory epilepsy neural cell cycle tetraploidy flow cytometry astrocytes |
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Epilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug‐resistant. The exact aetiology of... Epilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug-resistant. The exact aetiology of drug-resistant... AimsEpilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug‐resistant. The exact aetiology of drug‐resistant... |
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SubjectTerms | Amygdala Astrocytes Astrocytes - pathology Brain - pathology Drug resistance Epilepsy Epilepsy - pathology Epilepsy, Temporal Lobe - pathology Flow cytometry Hippocampus Hippocampus - pathology Humans Mental disorders neural cell cycle Neurological diseases Neurons Neurons - pathology polyploidy refractory epilepsy temporal lobe epilepsy Tetraploidy Tumor Suppressor Proteins |
Title | Neuronal and astrocytic tetraploidy is increased in drug‐resistant epilepsy |
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