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Complement component 3 (C3) expression in the hippocampus after excitotoxic injury: role of C/EBPβ
BACKGROUND: The CCAAT/enhancer-binding protein β (C/EBPβ) is a transcription factor implicated in the control of proliferation, differentiation, and inflammatory processes mainly in adipose tissue and liver; although more recent results have revealed an important role for this transcription factor i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073972/ https://www.ncbi.nlm.nih.gov/pubmed/27769255 http://dx.doi.org/10.1186/s12974-016-0742-0 |
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author | Hernandez-Encinas, Elena Aguilar-Morante, Diana Morales-Garcia, Jose A. Gine, Elena Sanz-SanCristobal, Marina Santos, Angel Perez-Castillo, Ana |
author_facet | Hernandez-Encinas, Elena Aguilar-Morante, Diana Morales-Garcia, Jose A. Gine, Elena Sanz-SanCristobal, Marina Santos, Angel Perez-Castillo, Ana |
author_sort | Hernandez-Encinas, Elena |
collection | PubMed |
description | BACKGROUND: The CCAAT/enhancer-binding protein β (C/EBPβ) is a transcription factor implicated in the control of proliferation, differentiation, and inflammatory processes mainly in adipose tissue and liver; although more recent results have revealed an important role for this transcription factor in the brain. Previous studies from our laboratory indicated that CCAAT/enhancer-binding protein β is implicated in inflammatory process and brain injury, since mice lacking this gene were less susceptible to kainic acid-induced injury. More recently, we have shown that the complement component 3 gene (C3) is a downstream target of CCAAT/enhancer-binding protein β and it could be a mediator of the proinflammatory effects of this transcription factor in neural cells. METHODS: Adult male Wistar rats (8–12 weeks old) were used throughout the study. C/EBPβ(+/+) and C/EBPβ(–/–) mice were generated from heterozygous breeding pairs. Animals were injected or not with kainic acid, brains removed, and brain slices containing the hippocampus analyzed for the expression of both CCAAT/enhancer-binding protein β and C3. RESULTS: In the present work, we have further extended these studies and show that CCAAT/enhancer-binding protein β and C3 co-express in the CA1 and CA3 regions of the hippocampus after an excitotoxic injury. Studies using CCAAT/enhancer-binding protein β knockout mice demonstrate a marked reduction in C3 expression after kainic acid injection in these animals, suggesting that indeed this protein is regulated by C/EBPβ in the hippocampus in vivo. CONCLUSIONS: Altogether these results suggest that CCAAT/enhancer-binding protein β could regulate brain disorders, in which excitotoxic and inflammatory processes are involved, at least in part through the direct regulation of C3. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12974-016-0742-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5073972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50739722016-10-27 Complement component 3 (C3) expression in the hippocampus after excitotoxic injury: role of C/EBPβ Hernandez-Encinas, Elena Aguilar-Morante, Diana Morales-Garcia, Jose A. Gine, Elena Sanz-SanCristobal, Marina Santos, Angel Perez-Castillo, Ana J Neuroinflammation Research BACKGROUND: The CCAAT/enhancer-binding protein β (C/EBPβ) is a transcription factor implicated in the control of proliferation, differentiation, and inflammatory processes mainly in adipose tissue and liver; although more recent results have revealed an important role for this transcription factor in the brain. Previous studies from our laboratory indicated that CCAAT/enhancer-binding protein β is implicated in inflammatory process and brain injury, since mice lacking this gene were less susceptible to kainic acid-induced injury. More recently, we have shown that the complement component 3 gene (C3) is a downstream target of CCAAT/enhancer-binding protein β and it could be a mediator of the proinflammatory effects of this transcription factor in neural cells. METHODS: Adult male Wistar rats (8–12 weeks old) were used throughout the study. C/EBPβ(+/+) and C/EBPβ(–/–) mice were generated from heterozygous breeding pairs. Animals were injected or not with kainic acid, brains removed, and brain slices containing the hippocampus analyzed for the expression of both CCAAT/enhancer-binding protein β and C3. RESULTS: In the present work, we have further extended these studies and show that CCAAT/enhancer-binding protein β and C3 co-express in the CA1 and CA3 regions of the hippocampus after an excitotoxic injury. Studies using CCAAT/enhancer-binding protein β knockout mice demonstrate a marked reduction in C3 expression after kainic acid injection in these animals, suggesting that indeed this protein is regulated by C/EBPβ in the hippocampus in vivo. CONCLUSIONS: Altogether these results suggest that CCAAT/enhancer-binding protein β could regulate brain disorders, in which excitotoxic and inflammatory processes are involved, at least in part through the direct regulation of C3. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12974-016-0742-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-21 /pmc/articles/PMC5073972/ /pubmed/27769255 http://dx.doi.org/10.1186/s12974-016-0742-0 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hernandez-Encinas, Elena Aguilar-Morante, Diana Morales-Garcia, Jose A. Gine, Elena Sanz-SanCristobal, Marina Santos, Angel Perez-Castillo, Ana Complement component 3 (C3) expression in the hippocampus after excitotoxic injury: role of C/EBPβ |
title | Complement component 3 (C3) expression in the hippocampus after excitotoxic injury: role of C/EBPβ |
title_full | Complement component 3 (C3) expression in the hippocampus after excitotoxic injury: role of C/EBPβ |
title_fullStr | Complement component 3 (C3) expression in the hippocampus after excitotoxic injury: role of C/EBPβ |
title_full_unstemmed | Complement component 3 (C3) expression in the hippocampus after excitotoxic injury: role of C/EBPβ |
title_short | Complement component 3 (C3) expression in the hippocampus after excitotoxic injury: role of C/EBPβ |
title_sort | complement component 3 (c3) expression in the hippocampus after excitotoxic injury: role of c/ebpβ |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073972/ https://www.ncbi.nlm.nih.gov/pubmed/27769255 http://dx.doi.org/10.1186/s12974-016-0742-0 |
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