Cargando…
Fish Granzyme A Shows a Greater Role Than Granzyme B in Fish Innate Cell-Mediated Cytotoxicity
Granzymes (Gzm) are serine proteases, contained into the secretory granules of cytotoxic cells, responsible for the cell-mediated cytotoxicity (CMC) against tumor cells and intracellular pathogens such as virus and bacteria. In fish, they have received little attention to their existence, classifica...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834543/ https://www.ncbi.nlm.nih.gov/pubmed/31736981 http://dx.doi.org/10.3389/fimmu.2019.02579 |
_version_ | 1783466495824625664 |
---|---|
author | Chaves-Pozo, Elena Valero, Yulema Lozano, Maria Teresa Rodríguez-Cerezo, Pablo Miao, Liang Campo, Vittorio Esteban, Maria Angeles Cuesta, Alberto |
author_facet | Chaves-Pozo, Elena Valero, Yulema Lozano, Maria Teresa Rodríguez-Cerezo, Pablo Miao, Liang Campo, Vittorio Esteban, Maria Angeles Cuesta, Alberto |
author_sort | Chaves-Pozo, Elena |
collection | PubMed |
description | Granzymes (Gzm) are serine proteases, contained into the secretory granules of cytotoxic cells, responsible for the cell-mediated cytotoxicity (CMC) against tumor cells and intracellular pathogens such as virus and bacteria. In fish, they have received little attention to their existence, classification or functional characterization. Therefore, we aimed to identify and evaluate their functional and transcriptomic relevance in the innate CMC activity of two relevant teleost fish species, gilthead seabream and European sea bass. Afterwards, we wanted to focus on their regulation upon nodavirus (NNV) infection, a virus that causes great mortalities to sea bass specimens while seabream is resistant. In this study, we have identified genes encoding GzmA and GzmB in both seabream and sea bass, as well as GzmM in seabream, which showed good phylogenetic relation to their mammalian orthologs. In addition, we found enzymatic activity related to tryptase (GzmA and/or GzmK), aspartase (GzmB), metase (GzmM), or chymase (GzmH) in resting head-kidney leucocytes (HKLs), with the following order of activity: GzmA/K ~ GzmM >> GzmH >>> GzmB. In addition, during innate CMC assays consisting on HKLs exposed to either mock- or NNV-infected target cells, though all the granzyme transcripts were increased only the tryptase activity did. Thus, our data suggest a high functional activity of GzmA/K in the innate CMC and a marginal one for GzmB. Moreover, GzmB activity was detected into target cells during the CMC assays. However, the percentage of target cells with GzmB activity after the CMC assays was about 10-fold lower than the death target cells, demonstrating that GzmB is not the main inductor of cell death. Moreover, in in vivo infection with NNV, gzm transcription is differently regulated depending on the fish species, genes and tissues. However, the immunohistochemistry study revealed an increased number of GzmB stained cells and areas in the brain of seabream after NNV infection, which was mainly associated with the lesions detected. Further studies are needed to ascertain the molecular nature, biological function and implication of fish granzymes in the CMC activity, and in the antiviral defense in particular. |
format | Online Article Text |
id | pubmed-6834543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68345432019-11-15 Fish Granzyme A Shows a Greater Role Than Granzyme B in Fish Innate Cell-Mediated Cytotoxicity Chaves-Pozo, Elena Valero, Yulema Lozano, Maria Teresa Rodríguez-Cerezo, Pablo Miao, Liang Campo, Vittorio Esteban, Maria Angeles Cuesta, Alberto Front Immunol Immunology Granzymes (Gzm) are serine proteases, contained into the secretory granules of cytotoxic cells, responsible for the cell-mediated cytotoxicity (CMC) against tumor cells and intracellular pathogens such as virus and bacteria. In fish, they have received little attention to their existence, classification or functional characterization. Therefore, we aimed to identify and evaluate their functional and transcriptomic relevance in the innate CMC activity of two relevant teleost fish species, gilthead seabream and European sea bass. Afterwards, we wanted to focus on their regulation upon nodavirus (NNV) infection, a virus that causes great mortalities to sea bass specimens while seabream is resistant. In this study, we have identified genes encoding GzmA and GzmB in both seabream and sea bass, as well as GzmM in seabream, which showed good phylogenetic relation to their mammalian orthologs. In addition, we found enzymatic activity related to tryptase (GzmA and/or GzmK), aspartase (GzmB), metase (GzmM), or chymase (GzmH) in resting head-kidney leucocytes (HKLs), with the following order of activity: GzmA/K ~ GzmM >> GzmH >>> GzmB. In addition, during innate CMC assays consisting on HKLs exposed to either mock- or NNV-infected target cells, though all the granzyme transcripts were increased only the tryptase activity did. Thus, our data suggest a high functional activity of GzmA/K in the innate CMC and a marginal one for GzmB. Moreover, GzmB activity was detected into target cells during the CMC assays. However, the percentage of target cells with GzmB activity after the CMC assays was about 10-fold lower than the death target cells, demonstrating that GzmB is not the main inductor of cell death. Moreover, in in vivo infection with NNV, gzm transcription is differently regulated depending on the fish species, genes and tissues. However, the immunohistochemistry study revealed an increased number of GzmB stained cells and areas in the brain of seabream after NNV infection, which was mainly associated with the lesions detected. Further studies are needed to ascertain the molecular nature, biological function and implication of fish granzymes in the CMC activity, and in the antiviral defense in particular. Frontiers Media S.A. 2019-10-31 /pmc/articles/PMC6834543/ /pubmed/31736981 http://dx.doi.org/10.3389/fimmu.2019.02579 Text en Copyright © 2019 Chaves-Pozo, Valero, Lozano, Rodríguez-Cerezo, Miao, Campo, Esteban and Cuesta. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Chaves-Pozo, Elena Valero, Yulema Lozano, Maria Teresa Rodríguez-Cerezo, Pablo Miao, Liang Campo, Vittorio Esteban, Maria Angeles Cuesta, Alberto Fish Granzyme A Shows a Greater Role Than Granzyme B in Fish Innate Cell-Mediated Cytotoxicity |
title | Fish Granzyme A Shows a Greater Role Than Granzyme B in Fish Innate Cell-Mediated Cytotoxicity |
title_full | Fish Granzyme A Shows a Greater Role Than Granzyme B in Fish Innate Cell-Mediated Cytotoxicity |
title_fullStr | Fish Granzyme A Shows a Greater Role Than Granzyme B in Fish Innate Cell-Mediated Cytotoxicity |
title_full_unstemmed | Fish Granzyme A Shows a Greater Role Than Granzyme B in Fish Innate Cell-Mediated Cytotoxicity |
title_short | Fish Granzyme A Shows a Greater Role Than Granzyme B in Fish Innate Cell-Mediated Cytotoxicity |
title_sort | fish granzyme a shows a greater role than granzyme b in fish innate cell-mediated cytotoxicity |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834543/ https://www.ncbi.nlm.nih.gov/pubmed/31736981 http://dx.doi.org/10.3389/fimmu.2019.02579 |
work_keys_str_mv | AT chavespozoelena fishgranzymeashowsagreaterrolethangranzymebinfishinnatecellmediatedcytotoxicity AT valeroyulema fishgranzymeashowsagreaterrolethangranzymebinfishinnatecellmediatedcytotoxicity AT lozanomariateresa fishgranzymeashowsagreaterrolethangranzymebinfishinnatecellmediatedcytotoxicity AT rodriguezcerezopablo fishgranzymeashowsagreaterrolethangranzymebinfishinnatecellmediatedcytotoxicity AT miaoliang fishgranzymeashowsagreaterrolethangranzymebinfishinnatecellmediatedcytotoxicity AT campovittorio fishgranzymeashowsagreaterrolethangranzymebinfishinnatecellmediatedcytotoxicity AT estebanmariaangeles fishgranzymeashowsagreaterrolethangranzymebinfishinnatecellmediatedcytotoxicity AT cuestaalberto fishgranzymeashowsagreaterrolethangranzymebinfishinnatecellmediatedcytotoxicity |