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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
Main Authors: Jurewicz, Anna, Matysiak, Mariola, Tybor, Krzysztof, Kilianek, Lukasz, Raine, Cedric S., Selmaj, Krzysztof
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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. 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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. 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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. 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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. 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identifier ISSN: 0006-8950
ispartof Brain (London, England : 1878), 2005-11, Vol.128 (11), p.2675-2688
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source Oxford Journals Online
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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