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The gene expression level of IFN-γR1 and IFN-γR2 in a murine model treated with Toxoplasma gondii and its products
AIM: To evaluate the effect of active T. gondii tachyzoites and its products on the gene expression level of IFN-γR1 and IFN-γR2 in a murine model. BACKGROUND: Many studies have shown that the parasite Toxoplasma gondii utilizes different mechanisms to inhibit the function of IFN-γ, but the parasite...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Shaheed Beheshti University of Medical Sciences
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833851/ https://www.ncbi.nlm.nih.gov/pubmed/27099672 |
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author | Kalani, Hamed Khanahmad Shahreza, Hosein Daryani, Ahmad Yousefi, Hosein Ali Pestechian, Nader Mansouri, Vahid |
author_facet | Kalani, Hamed Khanahmad Shahreza, Hosein Daryani, Ahmad Yousefi, Hosein Ali Pestechian, Nader Mansouri, Vahid |
author_sort | Kalani, Hamed |
collection | PubMed |
description | AIM: To evaluate the effect of active T. gondii tachyzoites and its products on the gene expression level of IFN-γR1 and IFN-γR2 in a murine model. BACKGROUND: Many studies have shown that the parasite Toxoplasma gondii utilizes different mechanisms to inhibit the function of IFN-γ, but the parasite effect on the function of IFN-γR1 and IFN-γR2 is still unclear. PATIENTS AND METHODS: Toxoplasma lysate product (TLP), excretory/secretory products (ESPs) obtained from cell free and cell culture media as well as active tachyzoites were injected separately to their respective group each consisted of 10 BALB/c mice. One control group of 10 mice received phosphate buffered saline (PBS). All of the mice were euthanized three days after the last injection and then their peritoneal leukocytes were harvested separately. The total RNA was extracted from the samples, converted to cDNA, and the gene expression level of IFN-γR1 and IFN-γR2 was assessed in all of the treated groups relative to the control one. RESULTS: There was no significant difference between each of the treated groups relative to the control group concerning the gene expression level of IFN-γR2 (P> 0.05). Furthermore, the gene expression level of IFN-γR1 in two groups of TLP (P= 0.04) and ESP obtained from cell free medium (P= 0.008) showed a significant difference relative to the control group. CONCLUSION: Findings of this study revealed a new aspect of host-T. gondii interaction in that this parasite is able to downregulate IFN-γR1 to reduce the IFN-γ effects on the infected cell. |
format | Online Article Text |
id | pubmed-4833851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Shaheed Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-48338512016-04-20 The gene expression level of IFN-γR1 and IFN-γR2 in a murine model treated with Toxoplasma gondii and its products Kalani, Hamed Khanahmad Shahreza, Hosein Daryani, Ahmad Yousefi, Hosein Ali Pestechian, Nader Mansouri, Vahid Gastroenterol Hepatol Bed Bench Original Article AIM: To evaluate the effect of active T. gondii tachyzoites and its products on the gene expression level of IFN-γR1 and IFN-γR2 in a murine model. BACKGROUND: Many studies have shown that the parasite Toxoplasma gondii utilizes different mechanisms to inhibit the function of IFN-γ, but the parasite effect on the function of IFN-γR1 and IFN-γR2 is still unclear. PATIENTS AND METHODS: Toxoplasma lysate product (TLP), excretory/secretory products (ESPs) obtained from cell free and cell culture media as well as active tachyzoites were injected separately to their respective group each consisted of 10 BALB/c mice. One control group of 10 mice received phosphate buffered saline (PBS). All of the mice were euthanized three days after the last injection and then their peritoneal leukocytes were harvested separately. The total RNA was extracted from the samples, converted to cDNA, and the gene expression level of IFN-γR1 and IFN-γR2 was assessed in all of the treated groups relative to the control one. RESULTS: There was no significant difference between each of the treated groups relative to the control group concerning the gene expression level of IFN-γR2 (P> 0.05). Furthermore, the gene expression level of IFN-γR1 in two groups of TLP (P= 0.04) and ESP obtained from cell free medium (P= 0.008) showed a significant difference relative to the control group. CONCLUSION: Findings of this study revealed a new aspect of host-T. gondii interaction in that this parasite is able to downregulate IFN-γR1 to reduce the IFN-γ effects on the infected cell. Shaheed Beheshti University of Medical Sciences 2016 /pmc/articles/PMC4833851/ /pubmed/27099672 Text en ©2016 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kalani, Hamed Khanahmad Shahreza, Hosein Daryani, Ahmad Yousefi, Hosein Ali Pestechian, Nader Mansouri, Vahid The gene expression level of IFN-γR1 and IFN-γR2 in a murine model treated with Toxoplasma gondii and its products |
title | The gene expression level of IFN-γR1 and IFN-γR2 in a murine model treated with Toxoplasma
gondii and its products |
title_full | The gene expression level of IFN-γR1 and IFN-γR2 in a murine model treated with Toxoplasma
gondii and its products |
title_fullStr | The gene expression level of IFN-γR1 and IFN-γR2 in a murine model treated with Toxoplasma
gondii and its products |
title_full_unstemmed | The gene expression level of IFN-γR1 and IFN-γR2 in a murine model treated with Toxoplasma
gondii and its products |
title_short | The gene expression level of IFN-γR1 and IFN-γR2 in a murine model treated with Toxoplasma
gondii and its products |
title_sort | gene expression level of ifn-γr1 and ifn-γr2 in a murine model treated with toxoplasma
gondii and its products |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833851/ https://www.ncbi.nlm.nih.gov/pubmed/27099672 |
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