Cargando…

Secretome Analysis of Host Cells Infected with Toxoplasma gondii after Treatment of Human Epidermal Growth Factor Receptor 2/4 Inhibitors

Toxoplasma gondii, a ubiquitous, intracellular parasite of the phylum Apicomplexa, infects an estimated one-third of the human population as well as a broad range of warm-blooded animals. We have observed that some tyrosine kinase inhibitors suppressed the growth of T. gondii within host ARPE-10 cel...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Hye-Jung, Ahn, Hye-Jin, Kang, Hyeweon, Park, Jaehui, Oh, Seul gi, Choi, Saehae, Lee, Won-Kyu, Nam, Ho-Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Parasitology and Tropical Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338902/
https://www.ncbi.nlm.nih.gov/pubmed/32615738
http://dx.doi.org/10.3347/kjp.2020.58.3.249
_version_ 1783554781571186688
author Kim, Hye-Jung
Ahn, Hye-Jin
Kang, Hyeweon
Park, Jaehui
Oh, Seul gi
Choi, Saehae
Lee, Won-Kyu
Nam, Ho-Woo
author_facet Kim, Hye-Jung
Ahn, Hye-Jin
Kang, Hyeweon
Park, Jaehui
Oh, Seul gi
Choi, Saehae
Lee, Won-Kyu
Nam, Ho-Woo
author_sort Kim, Hye-Jung
collection PubMed
description Toxoplasma gondii, a ubiquitous, intracellular parasite of the phylum Apicomplexa, infects an estimated one-third of the human population as well as a broad range of warm-blooded animals. We have observed that some tyrosine kinase inhibitors suppressed the growth of T. gondii within host ARPE-10 cells. Among them, afatinib, human epithermal growth factor receptor 2 and 4 (HER2/4) inhibitor, may be used as a therapeutic agent for inhibiting parasite growth with minimal adverse effects on host. In this report, we conducted a proteomic analysis to observe changes in host proteins that were altered via infection with T. gondii and the treatment of HER2/4 inhibitors. Secreting proteins were subjected to a procedure of micor basic reverse phase liquid chromatography, nano-liquid chromatography-mass spectrometry, and ingenuity pathway analysis serially. As a result, the expression level of heterogeneous nuclear ribonucleoprotein K, semaphorin 7A, a GPI membrane anchor, serine/threonine-protein phosphatase 2A, and calpain small subunit 1 proteins were significantly changed, and which were confirmed further by western blot analysis. Changes in various proteins, including these 4 proteins, can be used as a basis for explaining the effects of T. gondii infections and HER2/4 inhibitors.
format Online
Article
Text
id pubmed-7338902
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Korean Society for Parasitology and Tropical Medicine
record_format MEDLINE/PubMed
spelling pubmed-73389022020-07-16 Secretome Analysis of Host Cells Infected with Toxoplasma gondii after Treatment of Human Epidermal Growth Factor Receptor 2/4 Inhibitors Kim, Hye-Jung Ahn, Hye-Jin Kang, Hyeweon Park, Jaehui Oh, Seul gi Choi, Saehae Lee, Won-Kyu Nam, Ho-Woo Korean J Parasitol Original Article Toxoplasma gondii, a ubiquitous, intracellular parasite of the phylum Apicomplexa, infects an estimated one-third of the human population as well as a broad range of warm-blooded animals. We have observed that some tyrosine kinase inhibitors suppressed the growth of T. gondii within host ARPE-10 cells. Among them, afatinib, human epithermal growth factor receptor 2 and 4 (HER2/4) inhibitor, may be used as a therapeutic agent for inhibiting parasite growth with minimal adverse effects on host. In this report, we conducted a proteomic analysis to observe changes in host proteins that were altered via infection with T. gondii and the treatment of HER2/4 inhibitors. Secreting proteins were subjected to a procedure of micor basic reverse phase liquid chromatography, nano-liquid chromatography-mass spectrometry, and ingenuity pathway analysis serially. As a result, the expression level of heterogeneous nuclear ribonucleoprotein K, semaphorin 7A, a GPI membrane anchor, serine/threonine-protein phosphatase 2A, and calpain small subunit 1 proteins were significantly changed, and which were confirmed further by western blot analysis. Changes in various proteins, including these 4 proteins, can be used as a basis for explaining the effects of T. gondii infections and HER2/4 inhibitors. The Korean Society for Parasitology and Tropical Medicine 2020-06 2020-06-26 /pmc/articles/PMC7338902/ /pubmed/32615738 http://dx.doi.org/10.3347/kjp.2020.58.3.249 Text en Copyright © 2020 by The Korean Society for Parasitology and Tropical Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Hye-Jung
Ahn, Hye-Jin
Kang, Hyeweon
Park, Jaehui
Oh, Seul gi
Choi, Saehae
Lee, Won-Kyu
Nam, Ho-Woo
Secretome Analysis of Host Cells Infected with Toxoplasma gondii after Treatment of Human Epidermal Growth Factor Receptor 2/4 Inhibitors
title Secretome Analysis of Host Cells Infected with Toxoplasma gondii after Treatment of Human Epidermal Growth Factor Receptor 2/4 Inhibitors
title_full Secretome Analysis of Host Cells Infected with Toxoplasma gondii after Treatment of Human Epidermal Growth Factor Receptor 2/4 Inhibitors
title_fullStr Secretome Analysis of Host Cells Infected with Toxoplasma gondii after Treatment of Human Epidermal Growth Factor Receptor 2/4 Inhibitors
title_full_unstemmed Secretome Analysis of Host Cells Infected with Toxoplasma gondii after Treatment of Human Epidermal Growth Factor Receptor 2/4 Inhibitors
title_short Secretome Analysis of Host Cells Infected with Toxoplasma gondii after Treatment of Human Epidermal Growth Factor Receptor 2/4 Inhibitors
title_sort secretome analysis of host cells infected with toxoplasma gondii after treatment of human epidermal growth factor receptor 2/4 inhibitors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338902/
https://www.ncbi.nlm.nih.gov/pubmed/32615738
http://dx.doi.org/10.3347/kjp.2020.58.3.249
work_keys_str_mv AT kimhyejung secretomeanalysisofhostcellsinfectedwithtoxoplasmagondiiaftertreatmentofhumanepidermalgrowthfactorreceptor24inhibitors
AT ahnhyejin secretomeanalysisofhostcellsinfectedwithtoxoplasmagondiiaftertreatmentofhumanepidermalgrowthfactorreceptor24inhibitors
AT kanghyeweon secretomeanalysisofhostcellsinfectedwithtoxoplasmagondiiaftertreatmentofhumanepidermalgrowthfactorreceptor24inhibitors
AT parkjaehui secretomeanalysisofhostcellsinfectedwithtoxoplasmagondiiaftertreatmentofhumanepidermalgrowthfactorreceptor24inhibitors
AT ohseulgi secretomeanalysisofhostcellsinfectedwithtoxoplasmagondiiaftertreatmentofhumanepidermalgrowthfactorreceptor24inhibitors
AT choisaehae secretomeanalysisofhostcellsinfectedwithtoxoplasmagondiiaftertreatmentofhumanepidermalgrowthfactorreceptor24inhibitors
AT leewonkyu secretomeanalysisofhostcellsinfectedwithtoxoplasmagondiiaftertreatmentofhumanepidermalgrowthfactorreceptor24inhibitors
AT namhowoo secretomeanalysisofhostcellsinfectedwithtoxoplasmagondiiaftertreatmentofhumanepidermalgrowthfactorreceptor24inhibitors