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HBD3 Induces PD-L1 Expression on Head and Neck Squamous Cell Carcinoma Cell Lines
Human β-defensin 3 (HBD3) is an antimicrobial peptide up-regulated in the oral tissues of individuals with head and neck squamous cell carcinomas (HNSCC) and oral squamous cell carcinomas (SCC) and present in high concentrations in their saliva. In this study, we determined if HBD3 contributes to HN...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963492/ https://www.ncbi.nlm.nih.gov/pubmed/31554151 http://dx.doi.org/10.3390/antibiotics8040161 |
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author | Gomez Hernandez, Maria Paula Bates, Amber M. Starman, Emily E. Lanzel, Emily A. Comnick, Carissa Xie, Xian Jin Brogden, Kim A. |
author_facet | Gomez Hernandez, Maria Paula Bates, Amber M. Starman, Emily E. Lanzel, Emily A. Comnick, Carissa Xie, Xian Jin Brogden, Kim A. |
author_sort | Gomez Hernandez, Maria Paula |
collection | PubMed |
description | Human β-defensin 3 (HBD3) is an antimicrobial peptide up-regulated in the oral tissues of individuals with head and neck squamous cell carcinomas (HNSCC) and oral squamous cell carcinomas (SCC) and present in high concentrations in their saliva. In this study, we determined if HBD3 contributes to HNSCC pathogenesis by inducing programmed death-ligand 1 (PD-L1) expression on HNSCC cell lines. For this, SCC cell lines SCC4, SCC15, SCC19, SCC25, and SCC99 (5.0 × 10(4) viable cells) were used. Cells were incubated with IFNγ (0.6 µM) and HBD3 (0.2, 2.0, or 20.0 µM) for 24 h. Cells alone served as controls. Cells were then treated with anti-human APC-CD274 (PD-L1) and Live/Dead Fixable Green Dead Cell Stain. Cells treated with an isotype antibody and cells alone served as controls. All cell suspensions were analyzed in a LSR II Violet Flow Cytometer. Cytometric data was analyzed using FlowJo software. Treatment with IFNγ (0.6 µM) increased the number of cells expressing PD-L1 (p < 0.05) with respect to controls. Treatment with HBD3 (20.0 µM) also increased the number of cells expressing PD-L1 (p < 0.05) with respect to controls. However, treatment with IFNγ (0.6 µM) was not significantly different from treatment with HBD3 (20.0 µM) and the numbers of cells expressing PD-L1 were similar (p = 1). Thus, HBD3 increases the number of cells expressing PD-L1. This is a novel concept, but the role HBD3 contributes to HNSCC pathogenesis by inducing PD-L1 expression in tumors will have to be determined. |
format | Online Article Text |
id | pubmed-6963492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69634922020-01-30 HBD3 Induces PD-L1 Expression on Head and Neck Squamous Cell Carcinoma Cell Lines Gomez Hernandez, Maria Paula Bates, Amber M. Starman, Emily E. Lanzel, Emily A. Comnick, Carissa Xie, Xian Jin Brogden, Kim A. Antibiotics (Basel) Article Human β-defensin 3 (HBD3) is an antimicrobial peptide up-regulated in the oral tissues of individuals with head and neck squamous cell carcinomas (HNSCC) and oral squamous cell carcinomas (SCC) and present in high concentrations in their saliva. In this study, we determined if HBD3 contributes to HNSCC pathogenesis by inducing programmed death-ligand 1 (PD-L1) expression on HNSCC cell lines. For this, SCC cell lines SCC4, SCC15, SCC19, SCC25, and SCC99 (5.0 × 10(4) viable cells) were used. Cells were incubated with IFNγ (0.6 µM) and HBD3 (0.2, 2.0, or 20.0 µM) for 24 h. Cells alone served as controls. Cells were then treated with anti-human APC-CD274 (PD-L1) and Live/Dead Fixable Green Dead Cell Stain. Cells treated with an isotype antibody and cells alone served as controls. All cell suspensions were analyzed in a LSR II Violet Flow Cytometer. Cytometric data was analyzed using FlowJo software. Treatment with IFNγ (0.6 µM) increased the number of cells expressing PD-L1 (p < 0.05) with respect to controls. Treatment with HBD3 (20.0 µM) also increased the number of cells expressing PD-L1 (p < 0.05) with respect to controls. However, treatment with IFNγ (0.6 µM) was not significantly different from treatment with HBD3 (20.0 µM) and the numbers of cells expressing PD-L1 were similar (p = 1). Thus, HBD3 increases the number of cells expressing PD-L1. This is a novel concept, but the role HBD3 contributes to HNSCC pathogenesis by inducing PD-L1 expression in tumors will have to be determined. MDPI 2019-09-24 /pmc/articles/PMC6963492/ /pubmed/31554151 http://dx.doi.org/10.3390/antibiotics8040161 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gomez Hernandez, Maria Paula Bates, Amber M. Starman, Emily E. Lanzel, Emily A. Comnick, Carissa Xie, Xian Jin Brogden, Kim A. HBD3 Induces PD-L1 Expression on Head and Neck Squamous Cell Carcinoma Cell Lines |
title | HBD3 Induces PD-L1 Expression on Head and Neck Squamous Cell Carcinoma Cell Lines |
title_full | HBD3 Induces PD-L1 Expression on Head and Neck Squamous Cell Carcinoma Cell Lines |
title_fullStr | HBD3 Induces PD-L1 Expression on Head and Neck Squamous Cell Carcinoma Cell Lines |
title_full_unstemmed | HBD3 Induces PD-L1 Expression on Head and Neck Squamous Cell Carcinoma Cell Lines |
title_short | HBD3 Induces PD-L1 Expression on Head and Neck Squamous Cell Carcinoma Cell Lines |
title_sort | hbd3 induces pd-l1 expression on head and neck squamous cell carcinoma cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963492/ https://www.ncbi.nlm.nih.gov/pubmed/31554151 http://dx.doi.org/10.3390/antibiotics8040161 |
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