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Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin
Granulysin, a cationic protein expressed by human natural killer cells and cytotoxic T lymphocytes, is a mediator for drug-induced Stevens-Johnson syndrome and graft-versus-host disease. Some 15 kDa granulysin are processed into 9 kDa forms and sequestered in cytolytic granules, while others are con...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898823/ https://www.ncbi.nlm.nih.gov/pubmed/27276051 http://dx.doi.org/10.1371/journal.pone.0156321 |
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author | Wei, Hung-Mu Lin, Li-Chih Wang, Chiu-Feng Lee, Yi-Jang Chen, Yuan-Tsong Liao, You-Di |
author_facet | Wei, Hung-Mu Lin, Li-Chih Wang, Chiu-Feng Lee, Yi-Jang Chen, Yuan-Tsong Liao, You-Di |
author_sort | Wei, Hung-Mu |
collection | PubMed |
description | Granulysin, a cationic protein expressed by human natural killer cells and cytotoxic T lymphocytes, is a mediator for drug-induced Stevens-Johnson syndrome and graft-versus-host disease. Some 15 kDa granulysin are processed into 9 kDa forms and sequestered in cytolytic granules, while others are constitutively secreted into body fluids. Both 9 and 15 kDa granulysin have been shown to be a serum marker for cell-mediated immunity. Furthermore, 15 kDa is able to activate monocyte differentiation. However, its antimicrobial properties have not been clearly addressed. Here, we report a novel method to prepare both the soluble 9 and 15 kDa granulysin and show that the 15 kDa form is more effective than the 9 kDa form in exerting specific antimicrobial activity against Pseudomonas aeruginosa within a range of few micromolars. We also show that the 15 kDa granulysin is able to hyperpolarize the membrane potential and increase membrane permeability of treated bacteria. Interestingly, the bactericidal activity and membrane permeability of the granulysins were markedly reduced at lower pH (pH 5.4) as a result of probable increase in hydrophobicity of the granulysins. Additionally, we’ve also shown the granulysin to inhibit biofilm formation by P. aeruginosa. These results suggest that the 15 kDa granulysin exhibits a novel mechanism in bacteria killing in a way that’s different from most antimicrobial peptides. Our novel granulysin preparation methodology will be useful for further study of action mechanisms of other antimicrobial, cytotoxic and immunomodulating properties in granulysin-mediated diseases. |
format | Online Article Text |
id | pubmed-4898823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48988232016-06-16 Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin Wei, Hung-Mu Lin, Li-Chih Wang, Chiu-Feng Lee, Yi-Jang Chen, Yuan-Tsong Liao, You-Di PLoS One Research Article Granulysin, a cationic protein expressed by human natural killer cells and cytotoxic T lymphocytes, is a mediator for drug-induced Stevens-Johnson syndrome and graft-versus-host disease. Some 15 kDa granulysin are processed into 9 kDa forms and sequestered in cytolytic granules, while others are constitutively secreted into body fluids. Both 9 and 15 kDa granulysin have been shown to be a serum marker for cell-mediated immunity. Furthermore, 15 kDa is able to activate monocyte differentiation. However, its antimicrobial properties have not been clearly addressed. Here, we report a novel method to prepare both the soluble 9 and 15 kDa granulysin and show that the 15 kDa form is more effective than the 9 kDa form in exerting specific antimicrobial activity against Pseudomonas aeruginosa within a range of few micromolars. We also show that the 15 kDa granulysin is able to hyperpolarize the membrane potential and increase membrane permeability of treated bacteria. Interestingly, the bactericidal activity and membrane permeability of the granulysins were markedly reduced at lower pH (pH 5.4) as a result of probable increase in hydrophobicity of the granulysins. Additionally, we’ve also shown the granulysin to inhibit biofilm formation by P. aeruginosa. These results suggest that the 15 kDa granulysin exhibits a novel mechanism in bacteria killing in a way that’s different from most antimicrobial peptides. Our novel granulysin preparation methodology will be useful for further study of action mechanisms of other antimicrobial, cytotoxic and immunomodulating properties in granulysin-mediated diseases. Public Library of Science 2016-06-08 /pmc/articles/PMC4898823/ /pubmed/27276051 http://dx.doi.org/10.1371/journal.pone.0156321 Text en © 2016 Wei et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wei, Hung-Mu Lin, Li-Chih Wang, Chiu-Feng Lee, Yi-Jang Chen, Yuan-Tsong Liao, You-Di Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin |
title | Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin |
title_full | Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin |
title_fullStr | Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin |
title_full_unstemmed | Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin |
title_short | Antimicrobial Properties of an Immunomodulator - 15 kDa Human Granulysin |
title_sort | antimicrobial properties of an immunomodulator - 15 kda human granulysin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898823/ https://www.ncbi.nlm.nih.gov/pubmed/27276051 http://dx.doi.org/10.1371/journal.pone.0156321 |
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