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Ferroptotic agent‐induced endoplasmic reticulum stress response plays a pivotal role in the autophagic process outcome
Ferroptosis has been reported as a unique form of cell death. However, in recent years, researchers have increasingly challenged the uniqueness of ferroptosis compared to other types of cell death. In this study, we examined whether ferroptosis shares cell death pathways with other types of cell dea...
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Published in: | Journal of cellular physiology 2020-10, Vol.235 (10), p.6767-6778 |
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creator | Lee, Young‐Sun Kalimuthu, Kalishwaralal Seok Park, Yong Makala, Hima Watkins, Simon C. Choudry, M. Haroon A. Bartlett, David L. Tae Kwon, Yong Lee, Yong J. |
description | Ferroptosis has been reported as a unique form of cell death. However, in recent years, researchers have increasingly challenged the uniqueness of ferroptosis compared to other types of cell death. In this study, we examined whether ferroptosis shares cell death pathways with other types of cell death, especially autophagy, via the autophagic process. Here, we observed that ferroptosis inducers (artesunate [ART] and erastin [ERA]) and autophagy inducers (bortezomib [BOR] and XIE62‐1004) led to autophagosome formation via the endoplasmic reticulum (ER) stress response. Unlike XIE62‐1004, ART, ERA, and BOR, which affect glutathione production or utilization, induced oxidative stress responses—an increase in the levels of heme oxygenase‐1 and lipid peroxidation. Oxidative stress responses were attenuated by deletion of autophagy‐related gene‐5 or treatment with autophagy inhibitors (bafilomycin and chloroquine). Our studies provide an overview of common death pathways—the ER stress response‐associated autophagic process in ferroptosis and autophagy. We also highlight the role played by glutathione redox system in the outcome of the autophagic process.
The role played by glutathione redox system in the outcome of the autophagic process. |
doi_str_mv | 10.1002/jcp.29571 |
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The role played by glutathione redox system in the outcome of the autophagic process.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.29571</identifier><identifier>PMID: 31985039</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Apoptosis ; Apoptosis - physiology ; Artesunate ; Autophagosomes - metabolism ; Autophagosomes - physiology ; Autophagy ; Autophagy - physiology ; Bortezomib ; Cell death ; Cell Line, Tumor ; Cellular stress response ; Chloroquine ; Endoplasmic reticulum ; endoplasmic reticulum stress ; Endoplasmic Reticulum Stress - physiology ; Ferroptosis ; Ferroptosis - physiology ; Gene deletion ; Glutathione ; Glutathione - metabolism ; HCT116 Cells ; Heme ; Heme Oxygenase-1 - metabolism ; Humans ; Lipid peroxidation ; Lipid Peroxidation - physiology ; Lipids ; Mortality ; Oxidation-Reduction ; Oxidative stress ; Oxidative Stress - physiology ; Oxygenase ; Peroxidation ; Phagocytosis ; Signal Transduction - physiology</subject><ispartof>Journal of cellular physiology, 2020-10, Vol.235 (10), p.6767-6778</ispartof><rights>2020 Wiley Periodicals, Inc.</rights><rights>2020 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4431-981a1c4cb687672f849704e97711a7710d33f51bb9b5b162b374bd31b97891e43</citedby><cites>FETCH-LOGICAL-c4431-981a1c4cb687672f849704e97711a7710d33f51bb9b5b162b374bd31b97891e43</cites><orcidid>0000-0001-5914-8489</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31985039$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Young‐Sun</creatorcontrib><creatorcontrib>Kalimuthu, Kalishwaralal</creatorcontrib><creatorcontrib>Seok Park, Yong</creatorcontrib><creatorcontrib>Makala, Hima</creatorcontrib><creatorcontrib>Watkins, Simon C.</creatorcontrib><creatorcontrib>Choudry, M. Haroon A.</creatorcontrib><creatorcontrib>Bartlett, David L.</creatorcontrib><creatorcontrib>Tae Kwon, Yong</creatorcontrib><creatorcontrib>Lee, Yong J.</creatorcontrib><title>Ferroptotic agent‐induced endoplasmic reticulum stress response plays a pivotal role in the autophagic process outcome</title><title>Journal of cellular physiology</title><addtitle>J Cell Physiol</addtitle><description>Ferroptosis has been reported as a unique form of cell death. However, in recent years, researchers have increasingly challenged the uniqueness of ferroptosis compared to other types of cell death. In this study, we examined whether ferroptosis shares cell death pathways with other types of cell death, especially autophagy, via the autophagic process. Here, we observed that ferroptosis inducers (artesunate [ART] and erastin [ERA]) and autophagy inducers (bortezomib [BOR] and XIE62‐1004) led to autophagosome formation via the endoplasmic reticulum (ER) stress response. Unlike XIE62‐1004, ART, ERA, and BOR, which affect glutathione production or utilization, induced oxidative stress responses—an increase in the levels of heme oxygenase‐1 and lipid peroxidation. Oxidative stress responses were attenuated by deletion of autophagy‐related gene‐5 or treatment with autophagy inhibitors (bafilomycin and chloroquine). Our studies provide an overview of common death pathways—the ER stress response‐associated autophagic process in ferroptosis and autophagy. We also highlight the role played by glutathione redox system in the outcome of the autophagic process.
The role played by glutathione redox system in the outcome of the autophagic process.</description><subject>Apoptosis</subject><subject>Apoptosis - physiology</subject><subject>Artesunate</subject><subject>Autophagosomes - metabolism</subject><subject>Autophagosomes - physiology</subject><subject>Autophagy</subject><subject>Autophagy - physiology</subject><subject>Bortezomib</subject><subject>Cell death</subject><subject>Cell Line, Tumor</subject><subject>Cellular stress response</subject><subject>Chloroquine</subject><subject>Endoplasmic reticulum</subject><subject>endoplasmic reticulum stress</subject><subject>Endoplasmic Reticulum Stress - physiology</subject><subject>Ferroptosis</subject><subject>Ferroptosis - physiology</subject><subject>Gene deletion</subject><subject>Glutathione</subject><subject>Glutathione - metabolism</subject><subject>HCT116 Cells</subject><subject>Heme</subject><subject>Heme Oxygenase-1 - metabolism</subject><subject>Humans</subject><subject>Lipid peroxidation</subject><subject>Lipid Peroxidation - physiology</subject><subject>Lipids</subject><subject>Mortality</subject><subject>Oxidation-Reduction</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - physiology</subject><subject>Oxygenase</subject><subject>Peroxidation</subject><subject>Phagocytosis</subject><subject>Signal Transduction - physiology</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kcuKFDEUhoMoTju68AUk4EYXPZNbVSobQZoZLwzoQtchSZ3uTlNVKXMZ7d08gs_ok5i2x0EFNwnk__JxDj9CTyk5o4Sw852bz5hqJL2HFpQouRRtw-6jRc3oUjWCnqBHKe0IIUpx_hCdcKq6hnC1QN8uIcYw55C9w2YDU_5x891PfXHQY5j6MA8mjTWLUIkylBGnHCGl-pDmMCXAldgnbPDsr0M2A45hAOwnnLeATclh3ppNFcwxuMO_ULILIzxGD9ZmSPDk9j5Fny8vPq3eLq8-vHm3en21dELwOn1HDXXC2baTrWTrTihJBCgpKTX1ID3n64Zaq2xjacssl8L2nFolO0VB8FP06uidix2hd3XDaAY9Rz-auNfBeP13Mvmt3oRrLXnHlDwIXtwKYvhSIGU9-uRgGMwEoSTNuGhZ17bqgD7_B92FEqe6nmaCEyZFQ1mlXh4pF0NKEdZ3w1CiD33q2qf-1Wdln_05_R35u8AKnB-Br36A_f9N-v3q41H5EwqCrSk</recordid><startdate>202010</startdate><enddate>202010</enddate><creator>Lee, Young‐Sun</creator><creator>Kalimuthu, Kalishwaralal</creator><creator>Seok Park, Yong</creator><creator>Makala, Hima</creator><creator>Watkins, Simon C.</creator><creator>Choudry, M. Haroon A.</creator><creator>Bartlett, David L.</creator><creator>Tae Kwon, Yong</creator><creator>Lee, Yong J.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5914-8489</orcidid></search><sort><creationdate>202010</creationdate><title>Ferroptotic agent‐induced endoplasmic reticulum stress response plays a pivotal role in the autophagic process outcome</title><author>Lee, Young‐Sun ; Kalimuthu, Kalishwaralal ; Seok Park, Yong ; Makala, Hima ; Watkins, Simon C. ; Choudry, M. Haroon A. ; Bartlett, David L. ; Tae Kwon, Yong ; Lee, Yong J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4431-981a1c4cb687672f849704e97711a7710d33f51bb9b5b162b374bd31b97891e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Apoptosis</topic><topic>Apoptosis - physiology</topic><topic>Artesunate</topic><topic>Autophagosomes - metabolism</topic><topic>Autophagosomes - physiology</topic><topic>Autophagy</topic><topic>Autophagy - physiology</topic><topic>Bortezomib</topic><topic>Cell death</topic><topic>Cell Line, Tumor</topic><topic>Cellular stress response</topic><topic>Chloroquine</topic><topic>Endoplasmic reticulum</topic><topic>endoplasmic reticulum stress</topic><topic>Endoplasmic Reticulum Stress - physiology</topic><topic>Ferroptosis</topic><topic>Ferroptosis - physiology</topic><topic>Gene deletion</topic><topic>Glutathione</topic><topic>Glutathione - metabolism</topic><topic>HCT116 Cells</topic><topic>Heme</topic><topic>Heme Oxygenase-1 - metabolism</topic><topic>Humans</topic><topic>Lipid peroxidation</topic><topic>Lipid Peroxidation - physiology</topic><topic>Lipids</topic><topic>Mortality</topic><topic>Oxidation-Reduction</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - physiology</topic><topic>Oxygenase</topic><topic>Peroxidation</topic><topic>Phagocytosis</topic><topic>Signal Transduction - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Young‐Sun</creatorcontrib><creatorcontrib>Kalimuthu, Kalishwaralal</creatorcontrib><creatorcontrib>Seok Park, Yong</creatorcontrib><creatorcontrib>Makala, Hima</creatorcontrib><creatorcontrib>Watkins, Simon C.</creatorcontrib><creatorcontrib>Choudry, M. Haroon A.</creatorcontrib><creatorcontrib>Bartlett, David L.</creatorcontrib><creatorcontrib>Tae Kwon, Yong</creatorcontrib><creatorcontrib>Lee, Yong J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Young‐Sun</au><au>Kalimuthu, Kalishwaralal</au><au>Seok Park, Yong</au><au>Makala, Hima</au><au>Watkins, Simon C.</au><au>Choudry, M. Haroon A.</au><au>Bartlett, David L.</au><au>Tae Kwon, Yong</au><au>Lee, Yong J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ferroptotic agent‐induced endoplasmic reticulum stress response plays a pivotal role in the autophagic process outcome</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J Cell Physiol</addtitle><date>2020-10</date><risdate>2020</risdate><volume>235</volume><issue>10</issue><spage>6767</spage><epage>6778</epage><pages>6767-6778</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Ferroptosis has been reported as a unique form of cell death. However, in recent years, researchers have increasingly challenged the uniqueness of ferroptosis compared to other types of cell death. In this study, we examined whether ferroptosis shares cell death pathways with other types of cell death, especially autophagy, via the autophagic process. Here, we observed that ferroptosis inducers (artesunate [ART] and erastin [ERA]) and autophagy inducers (bortezomib [BOR] and XIE62‐1004) led to autophagosome formation via the endoplasmic reticulum (ER) stress response. Unlike XIE62‐1004, ART, ERA, and BOR, which affect glutathione production or utilization, induced oxidative stress responses—an increase in the levels of heme oxygenase‐1 and lipid peroxidation. Oxidative stress responses were attenuated by deletion of autophagy‐related gene‐5 or treatment with autophagy inhibitors (bafilomycin and chloroquine). Our studies provide an overview of common death pathways—the ER stress response‐associated autophagic process in ferroptosis and autophagy. We also highlight the role played by glutathione redox system in the outcome of the autophagic process.
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subjects | Apoptosis Apoptosis - physiology Artesunate Autophagosomes - metabolism Autophagosomes - physiology Autophagy Autophagy - physiology Bortezomib Cell death Cell Line, Tumor Cellular stress response Chloroquine Endoplasmic reticulum endoplasmic reticulum stress Endoplasmic Reticulum Stress - physiology Ferroptosis Ferroptosis - physiology Gene deletion Glutathione Glutathione - metabolism HCT116 Cells Heme Heme Oxygenase-1 - metabolism Humans Lipid peroxidation Lipid Peroxidation - physiology Lipids Mortality Oxidation-Reduction Oxidative stress Oxidative Stress - physiology Oxygenase Peroxidation Phagocytosis Signal Transduction - physiology |
title | Ferroptotic agent‐induced endoplasmic reticulum stress response plays a pivotal role in the autophagic process outcome |
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