Chlamydia and programmed cell death
Discordant views regarding host cell death induction by Chlamydia are likely owing to the different methods used for evaluation of apoptosis. Apoptotic and non-apoptotic death owing to both caspase-dependent and -independent activation of the Bax protein occur late in the productive growth cycle. Ev...
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Veröffentlicht in: | Current opinion in microbiology 2006-02, Vol.9 (1), p.102-108 |
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description | Discordant views regarding host cell death induction by
Chlamydia are likely owing to the different methods used for evaluation of apoptosis. Apoptotic and non-apoptotic death owing to both caspase-dependent and -independent activation of the Bax protein occur late in the productive growth cycle. Evidence also suggests that
Chlamydia inhibits apoptosis during productive growth as part of its intracellular survival strategy. This is in part owing to proteolytic degradation of the BH3-only family of pro-apoptotic proteins in the mitochondrial pathway.
Chlamydia also inhibits apoptosis during persistent growth or in phagocytes, but induces apoptosis in T cells, which suggests that apoptosis has an immunomodulatory role in chlamydial infections. The contribution of apoptosis in disease pathogenesis remains a focus for future research. |
doi_str_mv | 10.1016/j.mib.2005.12.004 |
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Chlamydia are likely owing to the different methods used for evaluation of apoptosis. Apoptotic and non-apoptotic death owing to both caspase-dependent and -independent activation of the Bax protein occur late in the productive growth cycle. Evidence also suggests that
Chlamydia inhibits apoptosis during productive growth as part of its intracellular survival strategy. This is in part owing to proteolytic degradation of the BH3-only family of pro-apoptotic proteins in the mitochondrial pathway.
Chlamydia also inhibits apoptosis during persistent growth or in phagocytes, but induces apoptosis in T cells, which suggests that apoptosis has an immunomodulatory role in chlamydial infections. The contribution of apoptosis in disease pathogenesis remains a focus for future research.</description><identifier>ISSN: 1369-5274</identifier><identifier>EISSN: 1879-0364</identifier><identifier>DOI: 10.1016/j.mib.2005.12.004</identifier><identifier>PMID: 16406838</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Apoptosis ; bcl-2-Associated X Protein - agonists ; BH3 Interacting Domain Death Agonist Protein - antagonists & inhibitors ; Chlamydia ; Chlamydia - immunology ; Chlamydia - pathogenicity ; Chlamydia Infections - immunology ; Chlamydia Infections - microbiology ; Humans ; Phagocytes - microbiology ; Phagocytes - pathology ; T-Lymphocytes - microbiology ; T-Lymphocytes - pathology</subject><ispartof>Current opinion in microbiology, 2006-02, Vol.9 (1), p.102-108</ispartof><rights>2005 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-b3ed008484cfecdbca083d937884e346badcd762008d21e872d9e37a722700453</citedby><cites>FETCH-LOGICAL-c382t-b3ed008484cfecdbca083d937884e346badcd762008d21e872d9e37a722700453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1369527405001980$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16406838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miyairi, Isao</creatorcontrib><creatorcontrib>Byrne, Gerald I</creatorcontrib><title>Chlamydia and programmed cell death</title><title>Current opinion in microbiology</title><addtitle>Curr Opin Microbiol</addtitle><description>Discordant views regarding host cell death induction by
Chlamydia are likely owing to the different methods used for evaluation of apoptosis. Apoptotic and non-apoptotic death owing to both caspase-dependent and -independent activation of the Bax protein occur late in the productive growth cycle. Evidence also suggests that
Chlamydia inhibits apoptosis during productive growth as part of its intracellular survival strategy. This is in part owing to proteolytic degradation of the BH3-only family of pro-apoptotic proteins in the mitochondrial pathway.
Chlamydia also inhibits apoptosis during persistent growth or in phagocytes, but induces apoptosis in T cells, which suggests that apoptosis has an immunomodulatory role in chlamydial infections. The contribution of apoptosis in disease pathogenesis remains a focus for future research.</description><subject>Apoptosis</subject><subject>bcl-2-Associated X Protein - agonists</subject><subject>BH3 Interacting Domain Death Agonist Protein - antagonists & inhibitors</subject><subject>Chlamydia</subject><subject>Chlamydia - immunology</subject><subject>Chlamydia - pathogenicity</subject><subject>Chlamydia Infections - immunology</subject><subject>Chlamydia Infections - microbiology</subject><subject>Humans</subject><subject>Phagocytes - microbiology</subject><subject>Phagocytes - pathology</subject><subject>T-Lymphocytes - microbiology</subject><subject>T-Lymphocytes - pathology</subject><issn>1369-5274</issn><issn>1879-0364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLAzEUhYMoVqs_wI0UBHcz3jwmyeBKii8ouNF1yCS3NmWmU5Op0H9vSgvudJW7-M7JxyHkikJJgcq7ZdmFpmQAVUlZCSCOyBnVqi6AS3Gcby7romJKjMh5SkvIRF3JUzKiUoDUXJ-Rm-mitd3WBzuxKz9Zx_4z2q5DP3HYthOPdlhckJO5bRNeHt4x-Xh6fJ--FLO359fpw6xwXLOhaDh6AC20cHN0vnEWNPc1V1oL5EI21juvZNbVnlHUivkaubKKMZXNKj4mt_vebPG1wTSYLqSdhl1hv0lGKsmhlupfkCrInzKeQboHXexTijg36xg6G7eGgtlNaJY52pjdhIYykzVy5vpQvmnyDr-Jw2YZuN8DmLf4DhhNcgFXDn2I6Abj-_BH_Q-SL38I</recordid><startdate>20060201</startdate><enddate>20060201</enddate><creator>Miyairi, Isao</creator><creator>Byrne, Gerald I</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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20060201</creationdate><title>Chlamydia and programmed cell death</title><author>Miyairi, Isao ; Byrne, Gerald I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-b3ed008484cfecdbca083d937884e346badcd762008d21e872d9e37a722700453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Apoptosis</topic><topic>bcl-2-Associated X Protein - agonists</topic><topic>BH3 Interacting Domain Death Agonist Protein - antagonists & inhibitors</topic><topic>Chlamydia</topic><topic>Chlamydia - immunology</topic><topic>Chlamydia - pathogenicity</topic><topic>Chlamydia Infections - immunology</topic><topic>Chlamydia Infections - microbiology</topic><topic>Humans</topic><topic>Phagocytes - microbiology</topic><topic>Phagocytes - pathology</topic><topic>T-Lymphocytes - microbiology</topic><topic>T-Lymphocytes - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miyairi, Isao</creatorcontrib><creatorcontrib>Byrne, Gerald I</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Current opinion in microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miyairi, Isao</au><au>Byrne, Gerald I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chlamydia and programmed cell death</atitle><jtitle>Current opinion in microbiology</jtitle><addtitle>Curr Opin Microbiol</addtitle><date>2006-02-01</date><risdate>2006</risdate><volume>9</volume><issue>1</issue><spage>102</spage><epage>108</epage><pages>102-108</pages><issn>1369-5274</issn><eissn>1879-0364</eissn><abstract>Discordant views regarding host cell death induction by
Chlamydia are likely owing to the different methods used for evaluation of apoptosis. Apoptotic and non-apoptotic death owing to both caspase-dependent and -independent activation of the Bax protein occur late in the productive growth cycle. Evidence also suggests that
Chlamydia inhibits apoptosis during productive growth as part of its intracellular survival strategy. This is in part owing to proteolytic degradation of the BH3-only family of pro-apoptotic proteins in the mitochondrial pathway.
Chlamydia also inhibits apoptosis during persistent growth or in phagocytes, but induces apoptosis in T cells, which suggests that apoptosis has an immunomodulatory role in chlamydial infections. The contribution of apoptosis in disease pathogenesis remains a focus for future research.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>16406838</pmid><doi>10.1016/j.mib.2005.12.004</doi><tpages>7</tpages></addata></record> |
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subjects | Apoptosis bcl-2-Associated X Protein - agonists BH3 Interacting Domain Death Agonist Protein - antagonists & inhibitors Chlamydia Chlamydia - immunology Chlamydia - pathogenicity Chlamydia Infections - immunology Chlamydia Infections - microbiology Humans Phagocytes - microbiology Phagocytes - pathology T-Lymphocytes - microbiology T-Lymphocytes - pathology |
title | Chlamydia and programmed cell death |
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