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Streptococcal pyrogenic exotoxin B inhibits apoptotic cell clearance by macrophages through protein S cleavage
Clearance of apoptotic cells by macrophages plays an important role in maintaining tissue homeostasis. Previous study indicated that streptococcal pyrogenic exotoxin B (SPE B) reduces phagocytic activity in group A streptococcus (GAS) infection. Here, we demonstrate that SPE B causes an inhibitory e...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867609/ https://www.ncbi.nlm.nih.gov/pubmed/27181595 http://dx.doi.org/10.1038/srep26026 |
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author | Chen, Chia-Ling Wu, Yueh-Ying Lin, Chiou-Feng Kuo, Chih-Feng Han, Chia-Li Wang, Shuying Chuang, Woei-Jer Chen, Chiu-Yueh Wu, Jiunn-Jong Tsai, Pei-Jane Liu, Ching-Chuan Lin, Yee-Shin |
author_facet | Chen, Chia-Ling Wu, Yueh-Ying Lin, Chiou-Feng Kuo, Chih-Feng Han, Chia-Li Wang, Shuying Chuang, Woei-Jer Chen, Chiu-Yueh Wu, Jiunn-Jong Tsai, Pei-Jane Liu, Ching-Chuan Lin, Yee-Shin |
author_sort | Chen, Chia-Ling |
collection | PubMed |
description | Clearance of apoptotic cells by macrophages plays an important role in maintaining tissue homeostasis. Previous study indicated that streptococcal pyrogenic exotoxin B (SPE B) reduces phagocytic activity in group A streptococcus (GAS) infection. Here, we demonstrate that SPE B causes an inhibitory effect on protein S-mediated phagocytosis. In the presence of SPE B, serum- and purified protein S-mediated phagocytosis of apoptotic cells were significantly inhibited. The binding abilities of protein S to apoptotic cells were decreased by treatment with SPE B. Bacterial culture supernatants from GAS NZ131 strain also caused a reduction of protein S binding to apoptotic cells, but speB mutant strain did not. SPE B directly cleaved protein S in vitro and in vivo, whereas a lower level of cleavage occurred in mice infected with a speB isogenic mutant strain. SPE B-mediated initial cleavage of protein S caused a disruption of phagocytosis, and also resulted in a loss of binding ability of protein S-associated C4b-binding protein to apoptotic cells. Taken together, these results suggest a novel pathogenic role of SPE B that initiates protein S degradation followed by the inhibition of apoptotic cell clearance by macrophages. |
format | Online Article Text |
id | pubmed-4867609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48676092016-05-31 Streptococcal pyrogenic exotoxin B inhibits apoptotic cell clearance by macrophages through protein S cleavage Chen, Chia-Ling Wu, Yueh-Ying Lin, Chiou-Feng Kuo, Chih-Feng Han, Chia-Li Wang, Shuying Chuang, Woei-Jer Chen, Chiu-Yueh Wu, Jiunn-Jong Tsai, Pei-Jane Liu, Ching-Chuan Lin, Yee-Shin Sci Rep Article Clearance of apoptotic cells by macrophages plays an important role in maintaining tissue homeostasis. Previous study indicated that streptococcal pyrogenic exotoxin B (SPE B) reduces phagocytic activity in group A streptococcus (GAS) infection. Here, we demonstrate that SPE B causes an inhibitory effect on protein S-mediated phagocytosis. In the presence of SPE B, serum- and purified protein S-mediated phagocytosis of apoptotic cells were significantly inhibited. The binding abilities of protein S to apoptotic cells were decreased by treatment with SPE B. Bacterial culture supernatants from GAS NZ131 strain also caused a reduction of protein S binding to apoptotic cells, but speB mutant strain did not. SPE B directly cleaved protein S in vitro and in vivo, whereas a lower level of cleavage occurred in mice infected with a speB isogenic mutant strain. SPE B-mediated initial cleavage of protein S caused a disruption of phagocytosis, and also resulted in a loss of binding ability of protein S-associated C4b-binding protein to apoptotic cells. Taken together, these results suggest a novel pathogenic role of SPE B that initiates protein S degradation followed by the inhibition of apoptotic cell clearance by macrophages. Nature Publishing Group 2016-05-16 /pmc/articles/PMC4867609/ /pubmed/27181595 http://dx.doi.org/10.1038/srep26026 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Chia-Ling Wu, Yueh-Ying Lin, Chiou-Feng Kuo, Chih-Feng Han, Chia-Li Wang, Shuying Chuang, Woei-Jer Chen, Chiu-Yueh Wu, Jiunn-Jong Tsai, Pei-Jane Liu, Ching-Chuan Lin, Yee-Shin Streptococcal pyrogenic exotoxin B inhibits apoptotic cell clearance by macrophages through protein S cleavage |
title | Streptococcal pyrogenic exotoxin B inhibits apoptotic cell clearance by macrophages through protein S cleavage |
title_full | Streptococcal pyrogenic exotoxin B inhibits apoptotic cell clearance by macrophages through protein S cleavage |
title_fullStr | Streptococcal pyrogenic exotoxin B inhibits apoptotic cell clearance by macrophages through protein S cleavage |
title_full_unstemmed | Streptococcal pyrogenic exotoxin B inhibits apoptotic cell clearance by macrophages through protein S cleavage |
title_short | Streptococcal pyrogenic exotoxin B inhibits apoptotic cell clearance by macrophages through protein S cleavage |
title_sort | streptococcal pyrogenic exotoxin b inhibits apoptotic cell clearance by macrophages through protein s cleavage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867609/ https://www.ncbi.nlm.nih.gov/pubmed/27181595 http://dx.doi.org/10.1038/srep26026 |
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