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Tumour necrosis factor-induced death of adult human oligodendrocytes is mediated by apoptosis inducing factor
Tumour necrosis factor (TNF)-induced death of oligodendrocytes, the cell type targeted in multiple sclerosis, is mediated by TNF receptor p55 (TNFR-p55). The ligation of TNFR-p55 induces several signal transduction pathways; however, the precise mechanism involved in human oligodendrocyte (hOL) deat...
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Published in: | Brain (London, England : 1878) England : 1878), 2005-11, Vol.128 (11), p.2675-2688 |
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container_title | Brain (London, England : 1878) |
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description | Tumour necrosis factor (TNF)-induced death of oligodendrocytes, the cell type targeted in multiple sclerosis, is mediated by TNF receptor p55 (TNFR-p55). The ligation of TNFR-p55 induces several signal transduction pathways; however, the precise mechanism involved in human oligodendrocyte (hOL) death is unknown. We defined that TNF-induced death of hOLs is non-caspase dependent, as evidenced by lack of generation of caspases 8, 1 and 3 active subunits; lack of cleavage of caspases 1 and 3 fluorogenic substrates; and lack of hOL death inhibition by the general caspase inhibitor, ZVAD.FMK. Electrophoresis of TNF-exposed hOL DNA revealed large-scale DNA fragmentation characteristic of apoptosis-inducing factor (AIF)-mediated cell death, and co-localization experiments showed that AIF translocation to the nucleus occurred upon exposure to TNF. AIF depletion by an antisense strategy prevented TNF-induced hOL death. These results indicate that TNF-induced death of hOLs is dependent on AIF, information of significance for the design strategies to protect hOLs during immune-mediated demyelination. |
doi_str_mv | 10.1093/brain/awh627 |
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The ligation of TNFR-p55 induces several signal transduction pathways; however, the precise mechanism involved in human oligodendrocyte (hOL) death is unknown. We defined that TNF-induced death of hOLs is non-caspase dependent, as evidenced by lack of generation of caspases 8, 1 and 3 active subunits; lack of cleavage of caspases 1 and 3 fluorogenic substrates; and lack of hOL death inhibition by the general caspase inhibitor, ZVAD.FMK. Electrophoresis of TNF-exposed hOL DNA revealed large-scale DNA fragmentation characteristic of apoptosis-inducing factor (AIF)-mediated cell death, and co-localization experiments showed that AIF translocation to the nucleus occurred upon exposure to TNF. AIF depletion by an antisense strategy prevented TNF-induced hOL death. These results indicate that TNF-induced death of hOLs is dependent on AIF, information of significance for the design strategies to protect hOLs during immune-mediated demyelination.</description><identifier>ISSN: 0006-8950</identifier><identifier>EISSN: 1460-2156</identifier><identifier>DOI: 10.1093/brain/awh627</identifier><identifier>PMID: 16219674</identifier><identifier>CODEN: BRAIAK</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; AIF = apoptosis-inducing factor ; Animals ; anti-GFAP = anti-glial fibrillary acidic protein ; anti-MBP = anti-myelin basic protein ; Apoptosis - drug effects ; apoptosis inducing factor ; Apoptosis Inducing Factor - antagonists & inhibitors ; Apoptosis Inducing Factor - physiology ; asAIF = antisense AIF ; Biological and medical sciences ; Calpain - physiology ; CASP8 and FADD-Like Apoptosis Regulating Protein ; Caspases - metabolism ; Cathepsins - physiology ; cell death ; Cell Death - drug effects ; Cell Death - physiology ; Cell Line ; DNA Fragmentation ; Drug toxicity and drugs side effects treatment ; FACS = fluorescence-activated cell sorter ; FADD = Fas-associated protein with death domain ; hOL = human oligodendrocyte ; Human viral diseases ; Humans ; Infectious diseases ; Inhibitor of Apoptosis Proteins - metabolism ; Intracellular Signaling Peptides and Proteins - metabolism ; Medical sciences ; Membrane Potentials - drug effects ; Mice ; Mitochondrial Membranes - drug effects ; Mitochondrial Membranes - physiology ; multiple sclerosis ; Neurology ; OL = oligodendrocyte ; oligodendrocytes ; Oligodendroglia - drug effects ; Oligodendroglia - pathology ; Pharmacology. Drug treatments ; PI = propidium iodide ; Poly (ADP-Ribose) Polymerase-1 ; Poly(ADP-ribose) Polymerases - metabolism ; Serine Endopeptidases - physiology ; Staurosporine - pharmacology ; TNF = tumour necrosis factor ; TNFR-p55 = TNF receptor p55 ; Toxicity: nervous system and muscle ; TPCK = N-tosyl-l-phenylalanine chloromethyl ketone ; TRADD = TNF-R1-associated death domain ; Translocation, Genetic ; Tumor Necrosis Factors - pharmacology ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids</subject><ispartof>Brain (London, England : 1878), 2005-11, Vol.128 (11), p.2675-2688</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Nov 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-efa10fb3ea05fc117e0610bb2bbbc5d7871dbe20320b22dd31d756ad93c67bd93</citedby><cites>FETCH-LOGICAL-c415t-efa10fb3ea05fc117e0610bb2bbbc5d7871dbe20320b22dd31d756ad93c67bd93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17251347$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16219674$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jurewicz, Anna</creatorcontrib><creatorcontrib>Matysiak, Mariola</creatorcontrib><creatorcontrib>Tybor, Krzysztof</creatorcontrib><creatorcontrib>Kilianek, Lukasz</creatorcontrib><creatorcontrib>Raine, Cedric S.</creatorcontrib><creatorcontrib>Selmaj, Krzysztof</creatorcontrib><title>Tumour necrosis factor-induced death of adult human oligodendrocytes is mediated by apoptosis inducing factor</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><description>Tumour necrosis factor (TNF)-induced death of oligodendrocytes, the cell type targeted in multiple sclerosis, is mediated by TNF receptor p55 (TNFR-p55). The ligation of TNFR-p55 induces several signal transduction pathways; however, the precise mechanism involved in human oligodendrocyte (hOL) death is unknown. We defined that TNF-induced death of hOLs is non-caspase dependent, as evidenced by lack of generation of caspases 8, 1 and 3 active subunits; lack of cleavage of caspases 1 and 3 fluorogenic substrates; and lack of hOL death inhibition by the general caspase inhibitor, ZVAD.FMK. Electrophoresis of TNF-exposed hOL DNA revealed large-scale DNA fragmentation characteristic of apoptosis-inducing factor (AIF)-mediated cell death, and co-localization experiments showed that AIF translocation to the nucleus occurred upon exposure to TNF. AIF depletion by an antisense strategy prevented TNF-induced hOL death. These results indicate that TNF-induced death of hOLs is dependent on AIF, information of significance for the design strategies to protect hOLs during immune-mediated demyelination.</description><subject>Adult</subject><subject>AIF = apoptosis-inducing factor</subject><subject>Animals</subject><subject>anti-GFAP = anti-glial fibrillary acidic protein</subject><subject>anti-MBP = anti-myelin basic protein</subject><subject>Apoptosis - drug effects</subject><subject>apoptosis inducing factor</subject><subject>Apoptosis Inducing Factor - antagonists & inhibitors</subject><subject>Apoptosis Inducing Factor - physiology</subject><subject>asAIF = antisense AIF</subject><subject>Biological and medical sciences</subject><subject>Calpain - physiology</subject><subject>CASP8 and FADD-Like Apoptosis Regulating Protein</subject><subject>Caspases - metabolism</subject><subject>Cathepsins - physiology</subject><subject>cell death</subject><subject>Cell Death - drug effects</subject><subject>Cell Death - physiology</subject><subject>Cell Line</subject><subject>DNA Fragmentation</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>FACS = fluorescence-activated cell sorter</subject><subject>FADD = Fas-associated protein with death domain</subject><subject>hOL = human oligodendrocyte</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Inhibitor of Apoptosis Proteins - metabolism</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Medical sciences</subject><subject>Membrane Potentials - drug effects</subject><subject>Mice</subject><subject>Mitochondrial Membranes - drug effects</subject><subject>Mitochondrial Membranes - physiology</subject><subject>multiple sclerosis</subject><subject>Neurology</subject><subject>OL = oligodendrocyte</subject><subject>oligodendrocytes</subject><subject>Oligodendroglia - drug effects</subject><subject>Oligodendroglia - pathology</subject><subject>Pharmacology. Drug treatments</subject><subject>PI = propidium iodide</subject><subject>Poly (ADP-Ribose) Polymerase-1</subject><subject>Poly(ADP-ribose) Polymerases - metabolism</subject><subject>Serine Endopeptidases - physiology</subject><subject>Staurosporine - pharmacology</subject><subject>TNF = tumour necrosis factor</subject><subject>TNFR-p55 = TNF receptor p55</subject><subject>Toxicity: nervous system and muscle</subject><subject>TPCK = N-tosyl-l-phenylalanine chloromethyl ketone</subject><subject>TRADD = TNF-R1-associated death domain</subject><subject>Translocation, Genetic</subject><subject>Tumor Necrosis Factors - pharmacology</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhi0EokvhxhlZSHAi1GPHdnKsCrRIK_FVJMTF8le6Lkm82Ilg_z3e3YhKXDjNYZ55pHlfhJ4CeQ2kZWcm6TCe6V8bQeU9tIJakIoCF_fRihAiqqbl5AQ9yvmWEKgZFQ_RCQgKrZD1Cg3X8xDnhEdvU8wh407bKaYqjG623mHn9bTBscPazf2EN_OgRxz7cBOdH12Kdjf5jMvd4F3QU7kwO6y3cTsdbAdNGG8W7WP0oNN99k-WeYq-vnt7fXFVrT9cvr84X1e2Bj5VvtNAOsO8JryzANITAcQYaoyx3MlGgjOeEkaJodQ5Bk5yoV3LrJCmjFP08ujdpvhz9nlSQ8jW970efZyzEo1kgrTwXxAkaxjQpoDP_wFvS2xjeUJBy2vGhKAFenWE9lnm5Du1TWHQaaeAqH1Z6lCWOpZV8GeLczYlvjt4aacALxZAZ6v7LunRhnzHScqB1XtRdeRCnvzvv3udfighmeTq6tt39fnjlzeSf1qrS_YHtiWvlQ</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Jurewicz, Anna</creator><creator>Matysiak, Mariola</creator><creator>Tybor, Krzysztof</creator><creator>Kilianek, Lukasz</creator><creator>Raine, Cedric S.</creator><creator>Selmaj, Krzysztof</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20051101</creationdate><title>Tumour necrosis factor-induced death of adult human oligodendrocytes is mediated by apoptosis inducing factor</title><author>Jurewicz, Anna ; Matysiak, Mariola ; Tybor, Krzysztof ; Kilianek, Lukasz ; Raine, Cedric S. ; Selmaj, Krzysztof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-efa10fb3ea05fc117e0610bb2bbbc5d7871dbe20320b22dd31d756ad93c67bd93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>AIF = apoptosis-inducing factor</topic><topic>Animals</topic><topic>anti-GFAP = anti-glial fibrillary acidic protein</topic><topic>anti-MBP = anti-myelin basic protein</topic><topic>Apoptosis - drug effects</topic><topic>apoptosis inducing factor</topic><topic>Apoptosis Inducing Factor - antagonists & inhibitors</topic><topic>Apoptosis Inducing Factor - physiology</topic><topic>asAIF = antisense AIF</topic><topic>Biological and medical sciences</topic><topic>Calpain - physiology</topic><topic>CASP8 and FADD-Like Apoptosis Regulating Protein</topic><topic>Caspases - metabolism</topic><topic>Cathepsins - physiology</topic><topic>cell death</topic><topic>Cell Death - drug effects</topic><topic>Cell Death - physiology</topic><topic>Cell Line</topic><topic>DNA Fragmentation</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>FACS = fluorescence-activated cell sorter</topic><topic>FADD = Fas-associated protein with death domain</topic><topic>hOL = human oligodendrocyte</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Inhibitor of Apoptosis Proteins - metabolism</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Medical sciences</topic><topic>Membrane Potentials - drug effects</topic><topic>Mice</topic><topic>Mitochondrial Membranes - drug effects</topic><topic>Mitochondrial Membranes - physiology</topic><topic>multiple sclerosis</topic><topic>Neurology</topic><topic>OL = oligodendrocyte</topic><topic>oligodendrocytes</topic><topic>Oligodendroglia - drug effects</topic><topic>Oligodendroglia - pathology</topic><topic>Pharmacology. Drug treatments</topic><topic>PI = propidium iodide</topic><topic>Poly (ADP-Ribose) Polymerase-1</topic><topic>Poly(ADP-ribose) Polymerases - metabolism</topic><topic>Serine Endopeptidases - physiology</topic><topic>Staurosporine - pharmacology</topic><topic>TNF = tumour necrosis factor</topic><topic>TNFR-p55 = TNF receptor p55</topic><topic>Toxicity: nervous system and muscle</topic><topic>TPCK = N-tosyl-l-phenylalanine chloromethyl ketone</topic><topic>TRADD = TNF-R1-associated death domain</topic><topic>Translocation, Genetic</topic><topic>Tumor Necrosis Factors - pharmacology</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jurewicz, Anna</creatorcontrib><creatorcontrib>Matysiak, Mariola</creatorcontrib><creatorcontrib>Tybor, Krzysztof</creatorcontrib><creatorcontrib>Kilianek, Lukasz</creatorcontrib><creatorcontrib>Raine, Cedric S.</creatorcontrib><creatorcontrib>Selmaj, Krzysztof</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain (London, England : 1878)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jurewicz, Anna</au><au>Matysiak, Mariola</au><au>Tybor, Krzysztof</au><au>Kilianek, Lukasz</au><au>Raine, Cedric S.</au><au>Selmaj, Krzysztof</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumour necrosis factor-induced death of adult human oligodendrocytes is mediated by apoptosis inducing factor</atitle><jtitle>Brain (London, England : 1878)</jtitle><addtitle>Brain</addtitle><date>2005-11-01</date><risdate>2005</risdate><volume>128</volume><issue>11</issue><spage>2675</spage><epage>2688</epage><pages>2675-2688</pages><issn>0006-8950</issn><eissn>1460-2156</eissn><coden>BRAIAK</coden><abstract>Tumour necrosis factor (TNF)-induced death of oligodendrocytes, the cell type targeted in multiple sclerosis, is mediated by TNF receptor p55 (TNFR-p55). The ligation of TNFR-p55 induces several signal transduction pathways; however, the precise mechanism involved in human oligodendrocyte (hOL) death is unknown. We defined that TNF-induced death of hOLs is non-caspase dependent, as evidenced by lack of generation of caspases 8, 1 and 3 active subunits; lack of cleavage of caspases 1 and 3 fluorogenic substrates; and lack of hOL death inhibition by the general caspase inhibitor, ZVAD.FMK. Electrophoresis of TNF-exposed hOL DNA revealed large-scale DNA fragmentation characteristic of apoptosis-inducing factor (AIF)-mediated cell death, and co-localization experiments showed that AIF translocation to the nucleus occurred upon exposure to TNF. AIF depletion by an antisense strategy prevented TNF-induced hOL death. These results indicate that TNF-induced death of hOLs is dependent on AIF, information of significance for the design strategies to protect hOLs during immune-mediated demyelination.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>16219674</pmid><doi>10.1093/brain/awh627</doi><tpages>14</tpages></addata></record> |
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subjects | Adult AIF = apoptosis-inducing factor Animals anti-GFAP = anti-glial fibrillary acidic protein anti-MBP = anti-myelin basic protein Apoptosis - drug effects apoptosis inducing factor Apoptosis Inducing Factor - antagonists & inhibitors Apoptosis Inducing Factor - physiology asAIF = antisense AIF Biological and medical sciences Calpain - physiology CASP8 and FADD-Like Apoptosis Regulating Protein Caspases - metabolism Cathepsins - physiology cell death Cell Death - drug effects Cell Death - physiology Cell Line DNA Fragmentation Drug toxicity and drugs side effects treatment FACS = fluorescence-activated cell sorter FADD = Fas-associated protein with death domain hOL = human oligodendrocyte Human viral diseases Humans Infectious diseases Inhibitor of Apoptosis Proteins - metabolism Intracellular Signaling Peptides and Proteins - metabolism Medical sciences Membrane Potentials - drug effects Mice Mitochondrial Membranes - drug effects Mitochondrial Membranes - physiology multiple sclerosis Neurology OL = oligodendrocyte oligodendrocytes Oligodendroglia - drug effects Oligodendroglia - pathology Pharmacology. Drug treatments PI = propidium iodide Poly (ADP-Ribose) Polymerase-1 Poly(ADP-ribose) Polymerases - metabolism Serine Endopeptidases - physiology Staurosporine - pharmacology TNF = tumour necrosis factor TNFR-p55 = TNF receptor p55 Toxicity: nervous system and muscle TPCK = N-tosyl-l-phenylalanine chloromethyl ketone TRADD = TNF-R1-associated death domain Translocation, Genetic Tumor Necrosis Factors - pharmacology Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids |
title | Tumour necrosis factor-induced death of adult human oligodendrocytes is mediated by apoptosis inducing factor |
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