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P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization
BACKGROUND: Polarization of microglia cells in the glioma microenvironment is closely related to the malignant progression and invasion of gliomas. Prolyl 4-hydroxylase subunit α1 (P4HA1) is the rate-limiting subunit of prolyl 4-hydroxylase (P4H). In previous studies, we showed that P4HA1 could prom...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954035/ https://www.ncbi.nlm.nih.gov/pubmed/33727827 http://dx.doi.org/10.2147/OTT.S299977 |
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author | Wang, Qiyan Zhang, Junwen Fang, Sheng Wang, Jialin Han, Xiangming Liu, Fusheng Jin, Guishan |
author_facet | Wang, Qiyan Zhang, Junwen Fang, Sheng Wang, Jialin Han, Xiangming Liu, Fusheng Jin, Guishan |
author_sort | Wang, Qiyan |
collection | PubMed |
description | BACKGROUND: Polarization of microglia cells in the glioma microenvironment is closely related to the malignant progression and invasion of gliomas. Prolyl 4-hydroxylase subunit α1 (P4HA1) is the rate-limiting subunit of prolyl 4-hydroxylase (P4H). In previous studies, we showed that P4HA1 could promote the proliferation, migration, and invasion of glioma cells, but the specific mechanisms through which this occurs have not been fully elucidated. MATERIALS AND METHODS: Interactions between glioma and microglia cells were analyzed using bioinformatics. Then, co-culture models were used to obtain conditioned media. To characterize microglial cell polarization, we used PCR and immunofluorescence. Proliferation and invasion assays were used to explore the biological behavior of glioma cells affected by microglia. Finally, marker expression was detected using immunohistochemistry in glioblastoma multiform (GBM) specimens. RESULTS: Knockdown of P4HA1 resulted in reduced chemotaxis of microglia toward GBM cells and increased polarization of microglia toward the M1 phenotype. The changed microglial polarization state, in turn, inhibited the proliferation and invasion of GBM cells. Moreover, in GBM tissue specimens, the P4HA1 expression level is negatively correlated with that of the CD86 microglia M1-specific marker. CONCLUSION: Our results show that P4HA1 promotes immunosuppressive microenvironment formation by cross-talk between GBM and microglia cells and indirectly increases the aggressiveness of GBM. |
format | Online Article Text |
id | pubmed-7954035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-79540352021-03-15 P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization Wang, Qiyan Zhang, Junwen Fang, Sheng Wang, Jialin Han, Xiangming Liu, Fusheng Jin, Guishan Onco Targets Ther Original Research BACKGROUND: Polarization of microglia cells in the glioma microenvironment is closely related to the malignant progression and invasion of gliomas. Prolyl 4-hydroxylase subunit α1 (P4HA1) is the rate-limiting subunit of prolyl 4-hydroxylase (P4H). In previous studies, we showed that P4HA1 could promote the proliferation, migration, and invasion of glioma cells, but the specific mechanisms through which this occurs have not been fully elucidated. MATERIALS AND METHODS: Interactions between glioma and microglia cells were analyzed using bioinformatics. Then, co-culture models were used to obtain conditioned media. To characterize microglial cell polarization, we used PCR and immunofluorescence. Proliferation and invasion assays were used to explore the biological behavior of glioma cells affected by microglia. Finally, marker expression was detected using immunohistochemistry in glioblastoma multiform (GBM) specimens. RESULTS: Knockdown of P4HA1 resulted in reduced chemotaxis of microglia toward GBM cells and increased polarization of microglia toward the M1 phenotype. The changed microglial polarization state, in turn, inhibited the proliferation and invasion of GBM cells. Moreover, in GBM tissue specimens, the P4HA1 expression level is negatively correlated with that of the CD86 microglia M1-specific marker. CONCLUSION: Our results show that P4HA1 promotes immunosuppressive microenvironment formation by cross-talk between GBM and microglia cells and indirectly increases the aggressiveness of GBM. Dove 2021-03-08 /pmc/articles/PMC7954035/ /pubmed/33727827 http://dx.doi.org/10.2147/OTT.S299977 Text en © 2021 Wang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Wang, Qiyan Zhang, Junwen Fang, Sheng Wang, Jialin Han, Xiangming Liu, Fusheng Jin, Guishan P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization |
title | P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization |
title_full | P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization |
title_fullStr | P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization |
title_full_unstemmed | P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization |
title_short | P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization |
title_sort | p4ha1 down-regulation inhibits glioma invasiveness by promoting m1 microglia polarization |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954035/ https://www.ncbi.nlm.nih.gov/pubmed/33727827 http://dx.doi.org/10.2147/OTT.S299977 |
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