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A Novel Therapeutic Reagent, KA-1002 for Alleviating Lysophosphatidic Acid-Mediated Inflammation Related Gene Expression in Swine Macrophages

SIMPLE SUMMARY: Inflammatory diseases are a key factor reducing the productivity of animals in a livestock industrial environment. We have identified a novel lysophosphatidic acid signaling antagonist, KA-1002, which alleviates lysophosphatidic acid-mediated a broad range of inflammation related gen...

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Autores principales: Hwang, Hyeon-Jeong, Park, Tamina, Kim, Miok, Shin, Hee-su, Hwang, Wooyeon, Min, Yong Ki, Song, Suk-gil, Park, Daeui, Lee, Chang Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142756/
https://www.ncbi.nlm.nih.gov/pubmed/32210054
http://dx.doi.org/10.3390/ani10030534
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author Hwang, Hyeon-Jeong
Park, Tamina
Kim, Miok
Shin, Hee-su
Hwang, Wooyeon
Min, Yong Ki
Song, Suk-gil
Park, Daeui
Lee, Chang Hoon
author_facet Hwang, Hyeon-Jeong
Park, Tamina
Kim, Miok
Shin, Hee-su
Hwang, Wooyeon
Min, Yong Ki
Song, Suk-gil
Park, Daeui
Lee, Chang Hoon
author_sort Hwang, Hyeon-Jeong
collection PubMed
description SIMPLE SUMMARY: Inflammatory diseases are a key factor reducing the productivity of animals in a livestock industrial environment. We have identified a novel lysophosphatidic acid signaling antagonist, KA-1002, which alleviates lysophosphatidic acid-mediated a broad range of inflammation related gene expression in swine macrophages. Specifically, we found that KA-1002 significantly alleviated LPA-induced genes related with inflammation such as a role of macrophages, fibroblasts and endothelial cells in rheumatoid arthritis and STAT3 signal pathway. Taken together, KA-1002 could be considered a novel therapeutic reagent candidate for swine inflammatory diseases. ABSTRACT: Stresses and various infectious reagents caused multiple inflammatory diseases in swine in a livestock industrial environment. Therefore, there is a need for an effective therapeutic or preventive agent that could alleviate chronic and acute inflammation. We found that lysophosphatidic acid (LPA), a stress-induced potent endogenous inflammatory molecule, causes a broad range-regulation of inflammation related genes inflammation in swine macrophages. We further investigated the genome scaled transcriptional regulatory effect of a novel LPA-signaling antagonist, KA-1002 on swine macrophages, inducing the alleviated LPA-mediated inflammation related gene expression. Therefore, KA-1002 could potentially serve as a novel therapeutic or preventive agent to maintain physiologically healthy and balanced conditions of pigs.
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spelling pubmed-71427562020-04-15 A Novel Therapeutic Reagent, KA-1002 for Alleviating Lysophosphatidic Acid-Mediated Inflammation Related Gene Expression in Swine Macrophages Hwang, Hyeon-Jeong Park, Tamina Kim, Miok Shin, Hee-su Hwang, Wooyeon Min, Yong Ki Song, Suk-gil Park, Daeui Lee, Chang Hoon Animals (Basel) Article SIMPLE SUMMARY: Inflammatory diseases are a key factor reducing the productivity of animals in a livestock industrial environment. We have identified a novel lysophosphatidic acid signaling antagonist, KA-1002, which alleviates lysophosphatidic acid-mediated a broad range of inflammation related gene expression in swine macrophages. Specifically, we found that KA-1002 significantly alleviated LPA-induced genes related with inflammation such as a role of macrophages, fibroblasts and endothelial cells in rheumatoid arthritis and STAT3 signal pathway. Taken together, KA-1002 could be considered a novel therapeutic reagent candidate for swine inflammatory diseases. ABSTRACT: Stresses and various infectious reagents caused multiple inflammatory diseases in swine in a livestock industrial environment. Therefore, there is a need for an effective therapeutic or preventive agent that could alleviate chronic and acute inflammation. We found that lysophosphatidic acid (LPA), a stress-induced potent endogenous inflammatory molecule, causes a broad range-regulation of inflammation related genes inflammation in swine macrophages. We further investigated the genome scaled transcriptional regulatory effect of a novel LPA-signaling antagonist, KA-1002 on swine macrophages, inducing the alleviated LPA-mediated inflammation related gene expression. Therefore, KA-1002 could potentially serve as a novel therapeutic or preventive agent to maintain physiologically healthy and balanced conditions of pigs. MDPI 2020-03-23 /pmc/articles/PMC7142756/ /pubmed/32210054 http://dx.doi.org/10.3390/ani10030534 Text en © 2020 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
Hwang, Hyeon-Jeong
Park, Tamina
Kim, Miok
Shin, Hee-su
Hwang, Wooyeon
Min, Yong Ki
Song, Suk-gil
Park, Daeui
Lee, Chang Hoon
A Novel Therapeutic Reagent, KA-1002 for Alleviating Lysophosphatidic Acid-Mediated Inflammation Related Gene Expression in Swine Macrophages
title A Novel Therapeutic Reagent, KA-1002 for Alleviating Lysophosphatidic Acid-Mediated Inflammation Related Gene Expression in Swine Macrophages
title_full A Novel Therapeutic Reagent, KA-1002 for Alleviating Lysophosphatidic Acid-Mediated Inflammation Related Gene Expression in Swine Macrophages
title_fullStr A Novel Therapeutic Reagent, KA-1002 for Alleviating Lysophosphatidic Acid-Mediated Inflammation Related Gene Expression in Swine Macrophages
title_full_unstemmed A Novel Therapeutic Reagent, KA-1002 for Alleviating Lysophosphatidic Acid-Mediated Inflammation Related Gene Expression in Swine Macrophages
title_short A Novel Therapeutic Reagent, KA-1002 for Alleviating Lysophosphatidic Acid-Mediated Inflammation Related Gene Expression in Swine Macrophages
title_sort novel therapeutic reagent, ka-1002 for alleviating lysophosphatidic acid-mediated inflammation related gene expression in swine macrophages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142756/
https://www.ncbi.nlm.nih.gov/pubmed/32210054
http://dx.doi.org/10.3390/ani10030534
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