Cargando…
OCT4B1 Regulates the Cellular Stress Response of Human Dental Pulp Cells with Inflammation
Introduction. Infection and apoptosis are combined triggers for inflammation in dental tissues. Octamer-binding transcription factor 4-B1 (OCT4B1), a novel spliced variant of OCT4 family, could respond to the cellular stress and possess antiapoptotic property. However, its specific role in dental pu...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394356/ https://www.ncbi.nlm.nih.gov/pubmed/28473980 http://dx.doi.org/10.1155/2017/2756891 |
_version_ | 1783229719699783680 |
---|---|
author | Liu, Lu Huang, Rong Yang, Ruiqi Wei, Xi |
author_facet | Liu, Lu Huang, Rong Yang, Ruiqi Wei, Xi |
author_sort | Liu, Lu |
collection | PubMed |
description | Introduction. Infection and apoptosis are combined triggers for inflammation in dental tissues. Octamer-binding transcription factor 4-B1 (OCT4B1), a novel spliced variant of OCT4 family, could respond to the cellular stress and possess antiapoptotic property. However, its specific role in dental pulpitis remains unknown. Methods. To investigate the effect of OCT4B1 on inflammation of dental pulp cells (DPCs), its expression in inflamed dental pulp tissues and DPCs was examined by in situ hybridization, real-time PCR, and FISH assay. OCT4B1 overexpressed DPCs model was established, confirmed by western blot and immunofluorescence staining, and then stimulated with Lipopolysaccharide (LPS). Apoptotic rate was determined by Hoechst/PI staining and FACS. Cell survival rate was calculated by CCK8 assay. Results. In situ hybridization, real-time PCR, and FISH assay revealed that OCT4B1 was extensively expressed in inflamed dental pulp tissues and DPCs with LPS stimulation. Western blot and immunofluorescence staining showed the expression of OCT4B1 and OCT4B increased after OCT4B1 transfection. Hoechst/PI staining and FACS demonstrated that less red/blue fluorescence was detected and apoptotic percentage decreased (3.45%) after transfection. CCK8 demonstrated that the survival rate of pCDH-OCT4B1-flag cells increased. Conclusions. OCT4B1 plays an essential role in inflammation and apoptosis of DPCs. OCT4B might operate synergistically with OCT4B1 to reduce apoptosis. |
format | Online Article Text |
id | pubmed-5394356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-53943562017-05-04 OCT4B1 Regulates the Cellular Stress Response of Human Dental Pulp Cells with Inflammation Liu, Lu Huang, Rong Yang, Ruiqi Wei, Xi Biomed Res Int Research Article Introduction. Infection and apoptosis are combined triggers for inflammation in dental tissues. Octamer-binding transcription factor 4-B1 (OCT4B1), a novel spliced variant of OCT4 family, could respond to the cellular stress and possess antiapoptotic property. However, its specific role in dental pulpitis remains unknown. Methods. To investigate the effect of OCT4B1 on inflammation of dental pulp cells (DPCs), its expression in inflamed dental pulp tissues and DPCs was examined by in situ hybridization, real-time PCR, and FISH assay. OCT4B1 overexpressed DPCs model was established, confirmed by western blot and immunofluorescence staining, and then stimulated with Lipopolysaccharide (LPS). Apoptotic rate was determined by Hoechst/PI staining and FACS. Cell survival rate was calculated by CCK8 assay. Results. In situ hybridization, real-time PCR, and FISH assay revealed that OCT4B1 was extensively expressed in inflamed dental pulp tissues and DPCs with LPS stimulation. Western blot and immunofluorescence staining showed the expression of OCT4B1 and OCT4B increased after OCT4B1 transfection. Hoechst/PI staining and FACS demonstrated that less red/blue fluorescence was detected and apoptotic percentage decreased (3.45%) after transfection. CCK8 demonstrated that the survival rate of pCDH-OCT4B1-flag cells increased. Conclusions. OCT4B1 plays an essential role in inflammation and apoptosis of DPCs. OCT4B might operate synergistically with OCT4B1 to reduce apoptosis. Hindawi 2017 2017-04-04 /pmc/articles/PMC5394356/ /pubmed/28473980 http://dx.doi.org/10.1155/2017/2756891 Text en Copyright © 2017 Lu Liu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Liu, Lu Huang, Rong Yang, Ruiqi Wei, Xi OCT4B1 Regulates the Cellular Stress Response of Human Dental Pulp Cells with Inflammation |
title | OCT4B1 Regulates the Cellular Stress Response of Human Dental Pulp Cells with Inflammation |
title_full | OCT4B1 Regulates the Cellular Stress Response of Human Dental Pulp Cells with Inflammation |
title_fullStr | OCT4B1 Regulates the Cellular Stress Response of Human Dental Pulp Cells with Inflammation |
title_full_unstemmed | OCT4B1 Regulates the Cellular Stress Response of Human Dental Pulp Cells with Inflammation |
title_short | OCT4B1 Regulates the Cellular Stress Response of Human Dental Pulp Cells with Inflammation |
title_sort | oct4b1 regulates the cellular stress response of human dental pulp cells with inflammation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394356/ https://www.ncbi.nlm.nih.gov/pubmed/28473980 http://dx.doi.org/10.1155/2017/2756891 |
work_keys_str_mv | AT liulu oct4b1regulatesthecellularstressresponseofhumandentalpulpcellswithinflammation AT huangrong oct4b1regulatesthecellularstressresponseofhumandentalpulpcellswithinflammation AT yangruiqi oct4b1regulatesthecellularstressresponseofhumandentalpulpcellswithinflammation AT weixi oct4b1regulatesthecellularstressresponseofhumandentalpulpcellswithinflammation |