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Stress-Induced Accumulation of HnRNP K into Stress Granules
Stress granules (SGs) are cytoplasmic aggregates to reprogram gene expression in response to cellular stimulus. Here, we show that while SGs are being assembled in response to clotrimazole, an antifungal medication heterogeneous nuclear ribonucleoprotein (hnRNP) K, an RNA-binding protein that mediat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955021/ https://www.ncbi.nlm.nih.gov/pubmed/35340804 http://dx.doi.org/10.26502/jcsct.5079129 |
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author | Kim, Jayoung Yeon, Austin Kim, Woong-Ki Kim, Khae-Hawn Ohn, Takbum |
author_facet | Kim, Jayoung Yeon, Austin Kim, Woong-Ki Kim, Khae-Hawn Ohn, Takbum |
author_sort | Kim, Jayoung |
collection | PubMed |
description | Stress granules (SGs) are cytoplasmic aggregates to reprogram gene expression in response to cellular stimulus. Here, we show that while SGs are being assembled in response to clotrimazole, an antifungal medication heterogeneous nuclear ribonucleoprotein (hnRNP) K, an RNA-binding protein that mediates translational silencing of mRNAs, is rapidly accumulated in SGs in U-2OS osteosarcoma cells. Forced expression of hnRNP K induces resistance to clotrimazole-induced apoptosis. Erk/MAPK is transiently activated in response to clotrimazole, and pharmacological suppression of the Erk/MAPK pathway sensitizes the cells to apoptosis. Inhibition of the Erk/MAPK pathway promotes the assembly of SGs. These results suggest that dynamic cytoplasmic formation of SGs and hnRNP K relocation to SGs may be defensive mechanisms against clotrimazole–induced apoptosis in U-2OS osteosarcoma cells. |
format | Online Article Text |
id | pubmed-8955021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-89550212022-03-25 Stress-Induced Accumulation of HnRNP K into Stress Granules Kim, Jayoung Yeon, Austin Kim, Woong-Ki Kim, Khae-Hawn Ohn, Takbum J Cancer Sci Clin Ther Article Stress granules (SGs) are cytoplasmic aggregates to reprogram gene expression in response to cellular stimulus. Here, we show that while SGs are being assembled in response to clotrimazole, an antifungal medication heterogeneous nuclear ribonucleoprotein (hnRNP) K, an RNA-binding protein that mediates translational silencing of mRNAs, is rapidly accumulated in SGs in U-2OS osteosarcoma cells. Forced expression of hnRNP K induces resistance to clotrimazole-induced apoptosis. Erk/MAPK is transiently activated in response to clotrimazole, and pharmacological suppression of the Erk/MAPK pathway sensitizes the cells to apoptosis. Inhibition of the Erk/MAPK pathway promotes the assembly of SGs. These results suggest that dynamic cytoplasmic formation of SGs and hnRNP K relocation to SGs may be defensive mechanisms against clotrimazole–induced apoptosis in U-2OS osteosarcoma cells. 2021 2021-10-15 /pmc/articles/PMC8955021/ /pubmed/35340804 http://dx.doi.org/10.26502/jcsct.5079129 Text en https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license 4.0 |
spellingShingle | Article Kim, Jayoung Yeon, Austin Kim, Woong-Ki Kim, Khae-Hawn Ohn, Takbum Stress-Induced Accumulation of HnRNP K into Stress Granules |
title | Stress-Induced Accumulation of HnRNP K into Stress Granules |
title_full | Stress-Induced Accumulation of HnRNP K into Stress Granules |
title_fullStr | Stress-Induced Accumulation of HnRNP K into Stress Granules |
title_full_unstemmed | Stress-Induced Accumulation of HnRNP K into Stress Granules |
title_short | Stress-Induced Accumulation of HnRNP K into Stress Granules |
title_sort | stress-induced accumulation of hnrnp k into stress granules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955021/ https://www.ncbi.nlm.nih.gov/pubmed/35340804 http://dx.doi.org/10.26502/jcsct.5079129 |
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