Cyclin D1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicity

G1-phase cyclin D1 (cD1) expression has been documented in post-mitotic neurons undergoing apoptosis, leading others to propose that attempted cell cycle re-entry may induce cell death. Here, cD1 immunoreactivity was found in a subpopulation of healthy excitatory neurons throughout the brain. Most s...

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Main Authors: Hajira B. Koeller, M. Elizabeth Ross, Sara B. Glickstein
Format: Article
Language:English
Published: Elsevier 2008-08-01
Series:Neurobiology of Disease
Subjects:
CA1
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996108000867
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spelling doaj-9ea60e73dc564d439214616c97d8389c2021-03-20T04:55:49ZengElsevierNeurobiology of Disease1095-953X2008-08-01312230241Cyclin D1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicityHajira B. Koeller0M. Elizabeth Ross1Sara B. Glickstein2Graduate Program in Neuroscience, Weill Medical College of Cornell University, 1300 York Avenue, Box 239, New York NY 10065, USA; Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York NY 10065, USAGraduate Program in Neuroscience, Weill Medical College of Cornell University, 1300 York Avenue, Box 239, New York NY 10065, USA; Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York NY 10065, USADepartment of Neurology and Neuroscience, Weill Medical College of Cornell University, New York NY 10065, USA; Corresponding author.G1-phase cyclin D1 (cD1) expression has been documented in post-mitotic neurons undergoing apoptosis, leading others to propose that attempted cell cycle re-entry may induce cell death. Here, cD1 immunoreactivity was found in a subpopulation of healthy excitatory neurons throughout the brain. Most striking was the selective cD1 expression in hippocampal pyramidal neurons, an especially vulnerable cell group. Seizure threshold, cD1 induction and CA1 neuron death were examined following application of kainate (KA) or pentylenetetrazole (PTZ) in cD1 heterozygous (+/−) and wildtype mice to determine whether baseline cD1 correlates with pathology. cD1+/− mice displayed resistance to KA, but not PTZ-induced seizures and had reduced or equivalent cytotoxicity respectively, compared with wildtype. KA administration, but not PTZ, induced cD1 expression. These findings suggest that basal cD1 expression may render hippocampal circuits more susceptible to particular epileptogenic agents and excitotoxic cell death, though cD1 is not a direct precipitant in apoptosis.http://www.sciencedirect.com/science/article/pii/S0969996108000867Cyclin D1KainatePentylenetetrazoleCA1ExcitotoxicitySeizure
collection DOAJ
language English
format Article
sources DOAJ
author Hajira B. Koeller
M. Elizabeth Ross
Sara B. Glickstein
spellingShingle Hajira B. Koeller
M. Elizabeth Ross
Sara B. Glickstein
Cyclin D1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicity
Neurobiology of Disease
Cyclin D1
Kainate
Pentylenetetrazole
CA1
Excitotoxicity
Seizure
author_facet Hajira B. Koeller
M. Elizabeth Ross
Sara B. Glickstein
author_sort Hajira B. Koeller
title Cyclin D1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicity
title_short Cyclin D1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicity
title_full Cyclin D1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicity
title_fullStr Cyclin D1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicity
title_full_unstemmed Cyclin D1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicity
title_sort cyclin d1 in excitatory neurons of the adult brain enhances kainate-induced neurotoxicity
publisher Elsevier
series Neurobiology of Disease
issn 1095-953X
publishDate 2008-08-01
description G1-phase cyclin D1 (cD1) expression has been documented in post-mitotic neurons undergoing apoptosis, leading others to propose that attempted cell cycle re-entry may induce cell death. Here, cD1 immunoreactivity was found in a subpopulation of healthy excitatory neurons throughout the brain. Most striking was the selective cD1 expression in hippocampal pyramidal neurons, an especially vulnerable cell group. Seizure threshold, cD1 induction and CA1 neuron death were examined following application of kainate (KA) or pentylenetetrazole (PTZ) in cD1 heterozygous (+/−) and wildtype mice to determine whether baseline cD1 correlates with pathology. cD1+/− mice displayed resistance to KA, but not PTZ-induced seizures and had reduced or equivalent cytotoxicity respectively, compared with wildtype. KA administration, but not PTZ, induced cD1 expression. These findings suggest that basal cD1 expression may render hippocampal circuits more susceptible to particular epileptogenic agents and excitotoxic cell death, though cD1 is not a direct precipitant in apoptosis.
topic Cyclin D1
Kainate
Pentylenetetrazole
CA1
Excitotoxicity
Seizure
url http://www.sciencedirect.com/science/article/pii/S0969996108000867
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AT melizabethross cyclind1inexcitatoryneuronsoftheadultbrainenhanceskainateinducedneurotoxicity
AT sarabglickstein cyclind1inexcitatoryneuronsoftheadultbrainenhanceskainateinducedneurotoxicity
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