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Secretion of biologically active interferon-gamma inducible protein-10 (IP-10) by Lactococcus lactis

BACKGROUND: Chemokines are a large group of chemotactic cytokines that regulate and direct migration of leukocytes, activate inflammatory responses, and are involved in many other functions including regulation of tumor development. Interferon-gamma inducible-protein-10 (IP-10) is a member of the C-...

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Autores principales: Villatoro-Hernandez, Julio, Loera-Arias, Maria J, Gamez-Escobedo, Anali, Franco-Molina, Moises, Gomez-Gutierrez, Jorge G, Rodriguez-Rocha, Humberto, Gutierrez-Puente, Yolanda, Saucedo-Cardenas, Odila, Valdes-Flores, Jesus, Montes-de-Oca-Luna, Roberto
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2503953/
https://www.ncbi.nlm.nih.gov/pubmed/18662403
http://dx.doi.org/10.1186/1475-2859-7-22
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author Villatoro-Hernandez, Julio
Loera-Arias, Maria J
Gamez-Escobedo, Anali
Franco-Molina, Moises
Gomez-Gutierrez, Jorge G
Rodriguez-Rocha, Humberto
Gutierrez-Puente, Yolanda
Saucedo-Cardenas, Odila
Valdes-Flores, Jesus
Montes-de-Oca-Luna, Roberto
author_facet Villatoro-Hernandez, Julio
Loera-Arias, Maria J
Gamez-Escobedo, Anali
Franco-Molina, Moises
Gomez-Gutierrez, Jorge G
Rodriguez-Rocha, Humberto
Gutierrez-Puente, Yolanda
Saucedo-Cardenas, Odila
Valdes-Flores, Jesus
Montes-de-Oca-Luna, Roberto
author_sort Villatoro-Hernandez, Julio
collection PubMed
description BACKGROUND: Chemokines are a large group of chemotactic cytokines that regulate and direct migration of leukocytes, activate inflammatory responses, and are involved in many other functions including regulation of tumor development. Interferon-gamma inducible-protein-10 (IP-10) is a member of the C-X-C subfamily of the chemokine family of cytokines. IP-10 specifically chemoattracts activated T lymphocytes, monocytes, and NK cells. IP-10 has been described also as a modulator of other antitumor cytokines. These properties make IP-10 a novel therapeutic molecule for the treatment of chronic and infectious diseases. Currently there are no suitable live biological systems to produce and secrete IP-10. Lactococcus lactis has been well-characterized over the years as a safe microorganism to produce heterologous proteins and to be used as a safe, live vaccine to deliver antigens and cytokines of interest. Here we report a recombinant strain of L. lactis genetically modified to produce and secrete biologically active IP-10. RESULTS: The IP-10 coding region was isolated from human cDNA and cloned into an L. lactis expression plasmid under the regulation of the pNis promoter. By fusion to the usp45 secretion signal, IP-10 was addressed out of the cell. Western blot analysis demonstrated that recombinant strains of L. lactis secrete IP-10 into the culture medium. Neither degradation nor incomplete forms of IP-10 were detected in the cell or supernatant fractions of L. lactis. In addition, we demonstrated that the NICE (nisin-controlled gene expression) system was able to express IP-10 "de novo" even two hours after nisin removal. This human IP-10 protein secreted by L. lactis was biological active as demonstrated by Chemotaxis assay over human CD3+T lymphocytes. CONCLUSION: Expression and secretion of mature IP-10 was efficiently achieved by L. lactis forming an effective system to produce IP-10. This recombinant IP-10 is biologically active as demonstrated by its ability to chemoattract human CD3+ T lymphocytes. This strain of recombinant L. lactis represents a potentially useful tool to be used as a live vaccine in vivo.
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spelling pubmed-25039532008-08-08 Secretion of biologically active interferon-gamma inducible protein-10 (IP-10) by Lactococcus lactis Villatoro-Hernandez, Julio Loera-Arias, Maria J Gamez-Escobedo, Anali Franco-Molina, Moises Gomez-Gutierrez, Jorge G Rodriguez-Rocha, Humberto Gutierrez-Puente, Yolanda Saucedo-Cardenas, Odila Valdes-Flores, Jesus Montes-de-Oca-Luna, Roberto Microb Cell Fact Research BACKGROUND: Chemokines are a large group of chemotactic cytokines that regulate and direct migration of leukocytes, activate inflammatory responses, and are involved in many other functions including regulation of tumor development. Interferon-gamma inducible-protein-10 (IP-10) is a member of the C-X-C subfamily of the chemokine family of cytokines. IP-10 specifically chemoattracts activated T lymphocytes, monocytes, and NK cells. IP-10 has been described also as a modulator of other antitumor cytokines. These properties make IP-10 a novel therapeutic molecule for the treatment of chronic and infectious diseases. Currently there are no suitable live biological systems to produce and secrete IP-10. Lactococcus lactis has been well-characterized over the years as a safe microorganism to produce heterologous proteins and to be used as a safe, live vaccine to deliver antigens and cytokines of interest. Here we report a recombinant strain of L. lactis genetically modified to produce and secrete biologically active IP-10. RESULTS: The IP-10 coding region was isolated from human cDNA and cloned into an L. lactis expression plasmid under the regulation of the pNis promoter. By fusion to the usp45 secretion signal, IP-10 was addressed out of the cell. Western blot analysis demonstrated that recombinant strains of L. lactis secrete IP-10 into the culture medium. Neither degradation nor incomplete forms of IP-10 were detected in the cell or supernatant fractions of L. lactis. In addition, we demonstrated that the NICE (nisin-controlled gene expression) system was able to express IP-10 "de novo" even two hours after nisin removal. This human IP-10 protein secreted by L. lactis was biological active as demonstrated by Chemotaxis assay over human CD3+T lymphocytes. CONCLUSION: Expression and secretion of mature IP-10 was efficiently achieved by L. lactis forming an effective system to produce IP-10. This recombinant IP-10 is biologically active as demonstrated by its ability to chemoattract human CD3+ T lymphocytes. This strain of recombinant L. lactis represents a potentially useful tool to be used as a live vaccine in vivo. BioMed Central 2008-07-28 /pmc/articles/PMC2503953/ /pubmed/18662403 http://dx.doi.org/10.1186/1475-2859-7-22 Text en Copyright © 2008 Villatoro-Hernandez et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Villatoro-Hernandez, Julio
Loera-Arias, Maria J
Gamez-Escobedo, Anali
Franco-Molina, Moises
Gomez-Gutierrez, Jorge G
Rodriguez-Rocha, Humberto
Gutierrez-Puente, Yolanda
Saucedo-Cardenas, Odila
Valdes-Flores, Jesus
Montes-de-Oca-Luna, Roberto
Secretion of biologically active interferon-gamma inducible protein-10 (IP-10) by Lactococcus lactis
title Secretion of biologically active interferon-gamma inducible protein-10 (IP-10) by Lactococcus lactis
title_full Secretion of biologically active interferon-gamma inducible protein-10 (IP-10) by Lactococcus lactis
title_fullStr Secretion of biologically active interferon-gamma inducible protein-10 (IP-10) by Lactococcus lactis
title_full_unstemmed Secretion of biologically active interferon-gamma inducible protein-10 (IP-10) by Lactococcus lactis
title_short Secretion of biologically active interferon-gamma inducible protein-10 (IP-10) by Lactococcus lactis
title_sort secretion of biologically active interferon-gamma inducible protein-10 (ip-10) by lactococcus lactis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2503953/
https://www.ncbi.nlm.nih.gov/pubmed/18662403
http://dx.doi.org/10.1186/1475-2859-7-22
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