Apoptosis Transcriptional Profile Induced by Porphyromonas gingivalis HmuY

This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs) derived from individuals with periodontitis (P) and healthy nonperiodontitis (NP) control subjects with P. gingivalis HmuY protein. PBMCs fro...

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Published inMediators of inflammation Vol. 2019; no. 2019; pp. 1 - 8
Main Authors Gomes-Filho, I. S., Olczak, T., Xavier, M. T., Trindade, S. C., Figueiredo, Camila A., Costa, Ryan S., Miranda, Patrícia M., Freitas, Sibelle A., Lopes, Mabel P. P., Pimentel, Ana C. M., Moura-Costa, Lilia F., Carvalho-Filho, Paulo C., Meyer, R.
Format Journal Article
LanguageEnglish
Published Cairo, Egypt Hindawi Publishing Corporation 01.01.2019
Hindawi
John Wiley & Sons, Inc
Wiley
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Online AccessGet full text
ISSN0962-9351
1466-1861
1466-1861
DOI10.1155/2019/6758159

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Abstract This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs) derived from individuals with periodontitis (P) and healthy nonperiodontitis (NP) control subjects with P. gingivalis HmuY protein. PBMCs from the P and NP groups were stimulated with HmuY P. gingivalis protein, and the expression of genes related to apoptosis was assessed by custom real-time polymerase chain reaction array (Custom RT2 PCR Array). Compared with the NP group, the P group showed low relative levels of apoptosis-related gene expression, downregulated for FAS, FAS ligand, TNFSF10 (TRAIL), BAK1, CASP9, and APAF1 after P. gingivalis HmuY protein stimulation. Furthermore, the P group exhibited low levels of relative gene expression, downregulated for CASP7 when the cells were not stimulated. Our data suggest that P. gingivalis HmuY protein might participate differently in the modulation of the intrinsic and extrinsic apoptosis pathways.
AbstractList This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs) derived from individuals with periodontitis (P) and healthy nonperiodontitis (NP) control subjects with P. gingivalis HmuY protein. PBMCs from the P and NP groups were stimulated with HmuY P. gingivalis protein, and the expression of genes related to apoptosis was assessed by custom real-time polymerase chain reaction array (Custom RT 2 PCR Array). Compared with the NP group, the P group showed low relative levels of apoptosis-related gene expression, downregulated for FAS, FAS ligand, TNFSF10 (TRAIL), BAK1, CASP9, and APAF1 after P. gingivalis HmuY protein stimulation. Furthermore, the P group exhibited low levels of relative gene expression, downregulated for CASP7 when the cells were not stimulated. Our data suggest that P. gingivalis HmuY protein might participate differently in the modulation of the intrinsic and extrinsic apoptosis pathways.
This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs) derived from individuals with periodontitis (P) and healthy nonperiodontitis (NP) control subjects with P. gingivalis HmuY protein. PBMCs from the P and NP groups were stimulated with HmuY P. gingivalis protein, and the expression of genes related to apoptosis was assessed by custom real-time polymerase chain reaction array (Custom RT2 PCR Array). Compared with the NP group, the P group showed low relative levels of apoptosis-related gene expression, downregulated for FAS, FAS ligand, TNFSF10 (TRAIL), BAK1, CASP9, and APAF1 after P. gingivalis HmuY protein stimulation. Furthermore, the P group exhibited low levels of relative gene expression, downregulated for CASP7 when the cells were not stimulated. Our data suggest that P. gingivalis HmuY protein might participate differently in the modulation of the intrinsic and extrinsic apoptosis pathways.
This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs) derived from individuals with periodontitis (P) and healthy nonperiodontitis (NP) control subjects with P. gingivalis HmuY protein. PBMCs from the P and NP groups were stimulated with HmuY P. gingivalis protein, and the expression of genes related to apoptosis was assessed by custom real-time polymerase chain reaction array (Custom RT2 PCR Array). Compared with the NP group, the P group showed low relative levels of apoptosis-related gene expression, downregulated for FAS, FAS ligand, TNFSF10 (TRAIL), BAK1, CASP9, and APAF1 after P. gingivalis HmuY protein stimulation. Furthermore, the P group exhibited low levels of relative gene expression, downregulated for CASP7 when the cells were not stimulated. Our data suggest that P. gingivalis HmuY protein might participate differently in the modulation of the intrinsic and extrinsic apoptosis pathways.This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs) derived from individuals with periodontitis (P) and healthy nonperiodontitis (NP) control subjects with P. gingivalis HmuY protein. PBMCs from the P and NP groups were stimulated with HmuY P. gingivalis protein, and the expression of genes related to apoptosis was assessed by custom real-time polymerase chain reaction array (Custom RT2 PCR Array). Compared with the NP group, the P group showed low relative levels of apoptosis-related gene expression, downregulated for FAS, FAS ligand, TNFSF10 (TRAIL), BAK1, CASP9, and APAF1 after P. gingivalis HmuY protein stimulation. Furthermore, the P group exhibited low levels of relative gene expression, downregulated for CASP7 when the cells were not stimulated. Our data suggest that P. gingivalis HmuY protein might participate differently in the modulation of the intrinsic and extrinsic apoptosis pathways.
This study aimed at evaluating the transcriptional profile of apoptosis-related genes after stimulation of peripheral blood mononuclear cells (PBMCs) derived from individuals with periodontitis (P) and healthy nonperiodontitis (NP) control subjects with HmuY protein. PBMCs from the P and NP groups were stimulated with HmuY protein, and the expression of genes related to apoptosis was assessed by custom real-time polymerase chain reaction array (Custom RT PCR Array). Compared with the NP group, the P group showed low relative levels of apoptosis-related gene expression, downregulated for FAS, FAS ligand, TNFSF10 (TRAIL), BAK1, CASP9, and APAF1 after HmuY protein stimulation. Furthermore, the P group exhibited low levels of relative gene expression, downregulated for CASP7 when the cells were not stimulated. Our data suggest that HmuY protein might participate differently in the modulation of the intrinsic and extrinsic apoptosis pathways.
This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs) derived from individuals with periodontitis (P) and healthy nonperiodontitis (NP) control subjects with P. gingivalis HmuY protein. PBMCs from the P and NP groups were stimulated with HmuY P. gingivalis protein, and the expression of genes related to apoptosis was assessed by custom real-time polymerase chain reaction array (Custom R[T.sup.2] PCR Array). Compared with the NP group, the P group showed low relative levels of apoptosis-related gene expression, downregulated for FAS, FAS ligand, TNFSF10 (TRAIL), BAK1, CASP9, and APAF1 after P. gingivalis HmuY protein stimulation. Furthermore, the P group exhibited low levels of relative gene expression, downregulated for CASP7 when the cells were not stimulated. Our data suggest that P. gingivalis HmuY protein might participate differently in the modulation of the intrinsic and extrinsic apoptosis pathways.
Audience Academic
Author Freitas, Sibelle A.
Pimentel, Ana C. M.
Carvalho-Filho, Paulo C.
Gomes-Filho, I. S.
Figueiredo, Camila A.
Moura-Costa, Lilia F.
Meyer, R.
Xavier, M. T.
Lopes, Mabel P. P.
Costa, Ryan S.
Miranda, Patrícia M.
Trindade, S. C.
Olczak, T.
AuthorAffiliation 2 Dental School, Bahiana School of Medicine and Public Health, Brazil
4 Laboratory of Medical Biology, Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland
3 Department of Periodontics, Feira de Santana State University, Bahia, Brazil
1 Department of Immunology, Federal University of Bahia, Bahia, Brazil
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ContentType Journal Article
Copyright Copyright © 2019 Paulo C. Carvalho-Filho et al.
COPYRIGHT 2019 John Wiley & Sons, Inc.
Copyright © 2019 Paulo C. Carvalho-Filho et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0
Copyright © 2019 Paulo C. Carvalho-Filho et al. 2019
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– notice: Copyright © 2019 Paulo C. Carvalho-Filho et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0
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Snippet This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs)...
This study aimed at evaluating the transcriptional profile of apoptosis-related genes after in vitro stimulation of peripheral blood mononuclear cells (PBMCs)...
This study aimed at evaluating the transcriptional profile of apoptosis-related genes after stimulation of peripheral blood mononuclear cells (PBMCs) derived...
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StartPage 1
SubjectTerms Antigens
Apoptosis
Apoptosis - genetics
Apoptosis - physiology
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Biofilms
Biology
Cytokines
Disease
FasL protein
Gene expression
Genes
Genetic aspects
Genetic transcription
HmuY protein
Humans
Infections
Inflammation
Leukocytes (mononuclear)
Leukocytes, Mononuclear - metabolism
Leukocytes, Mononuclear - microbiology
Pathogens
Periodontitis
Peripheral blood mononuclear cells
Polymerase chain reaction
Porphyromonas gingivalis - metabolism
Porphyromonas gingivalis - pathogenicity
Proteins
Real-Time Polymerase Chain Reaction
TRAIL protein
Transcription
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Title Apoptosis Transcriptional Profile Induced by Porphyromonas gingivalis HmuY
URI https://search.emarefa.net/detail/BIM-1193166
https://dx.doi.org/10.1155/2019/6758159
https://www.ncbi.nlm.nih.gov/pubmed/31011284
https://www.proquest.com/docview/2200606128
https://www.proquest.com/docview/2213157559
https://pubmed.ncbi.nlm.nih.gov/PMC6442302
https://doaj.org/article/7a810b0c49ff41edabcd22f58beb5edc
Volume 2019
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