Apoptosis, autophagy, and more
Cell death has been subdivided into the categories apoptosis (Type I), autophagic cell death (Type II), and necrosis (Type III). The boundary between Type I and II has never been completely clear and perhaps does not exist due to intrinsic factors among different cell types and the crosstalk among o...
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Veröffentlicht in: | International Journal of Biochemistry and Cell Biology 2004-12, Vol.36 (12), p.2405-2419 |
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creator | Lockshin, Richard A. Zakeri, Zahra |
description | Cell death has been subdivided into the categories apoptosis (Type I), autophagic cell death (Type II), and necrosis (Type III). The boundary between Type I and II has never been completely clear and perhaps does not exist due to intrinsic factors among different cell types and the crosstalk among organelles within each type. Apoptosis can begin with autophagy, autophagy can end with apoptosis, and blockage of caspase activity can cause a cell to default to Type II cell death from Type I. Furthermore, autophagy is a normal physiological process active in both homeostasis (organelle turnover) and atrophy. “Autophagic cell death” may be interpreted as the process of autophagy that, unlike other situations, does not terminate before the cell collapses. Since switching among the alternative pathways to death is relatively common, interpretations based on knockouts or inhibitors, and therapies directed at controlling apoptosis must include these considerations. |
doi_str_mv | 10.1016/j.biocel.2004.04.011 |
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The boundary between Type I and II has never been completely clear and perhaps does not exist due to intrinsic factors among different cell types and the crosstalk among organelles within each type. Apoptosis can begin with autophagy, autophagy can end with apoptosis, and blockage of caspase activity can cause a cell to default to Type II cell death from Type I. Furthermore, autophagy is a normal physiological process active in both homeostasis (organelle turnover) and atrophy. “Autophagic cell death” may be interpreted as the process of autophagy that, unlike other situations, does not terminate before the cell collapses. 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Since switching among the alternative pathways to death is relatively common, interpretations based on knockouts or inhibitors, and therapies directed at controlling apoptosis must include these considerations.</description><subject>Animals</subject><subject>Apoptosis - physiology</subject><subject>Autophagy - physiology</subject><subject>Cell Death - physiology</subject><subject>Humans</subject><subject>Lysosomes - metabolism</subject><issn>1357-2725</issn><issn>1878-5875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UE1LAzEUDKJYrf4DKT15cte8fGzSi1CKX1DwoueQzb7VlLZZk12h_95dtuBNePDmMDPvzRByAzQHCsX9Ji99cLjNGaUiHwbghFyAVjqTWsnTHnOpMqaYnJDLlDaUUpCMn5MJSM6k1HBBZssmNG1IPt3NbdeG5st-Hnq4r-a7EPGKnNV2m_D6uKfk4-nxffWSrd-eX1fLdea41G22QEBhFS-4LQCsc-jqsgaHUgthC8UFKxWrnXS0Yq7ktbaLUjCuBIiK1Qs-JbejbxPDd4epNTuf-nBbu8fQJVMUmmro354SMRJdDClFrE0T_c7GgwFqhl7Mxoy9mKEXMwxAL5sd_btyh9Wf6FhET3gYCdin_PEYTXIe9w4rH9G1pgr-_wu_dL50EA</recordid><startdate>20041201</startdate><enddate>20041201</enddate><creator>Lockshin, Richard A.</creator><creator>Zakeri, Zahra</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>20041201</creationdate><title>Apoptosis, autophagy, and more</title><author>Lockshin, Richard A. ; Zakeri, Zahra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-9e1e4a7363a611accecfbf1ce5844a67342b72fc5c0d2cb3f8a9b4237414d2f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Apoptosis - physiology</topic><topic>Autophagy - physiology</topic><topic>Cell Death - physiology</topic><topic>Humans</topic><topic>Lysosomes - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lockshin, Richard A.</creatorcontrib><creatorcontrib>Zakeri, Zahra</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International Journal of Biochemistry and Cell Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lockshin, Richard A.</au><au>Zakeri, Zahra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apoptosis, autophagy, and more</atitle><jtitle>International Journal of Biochemistry and Cell Biology</jtitle><addtitle>Int J Biochem Cell Biol</addtitle><date>2004-12-01</date><risdate>2004</risdate><volume>36</volume><issue>12</issue><spage>2405</spage><epage>2419</epage><pages>2405-2419</pages><issn>1357-2725</issn><eissn>1878-5875</eissn><abstract>Cell death has been subdivided into the categories apoptosis (Type I), autophagic cell death (Type II), and necrosis (Type III). 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subjects | Animals Apoptosis - physiology Autophagy - physiology Cell Death - physiology Humans Lysosomes - metabolism |
title | Apoptosis, autophagy, and more |
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