Expression of the inhibitor of apoptosis protein family in multiple sclerosis reveals a potential immunomodulatory role during autoimmune mediated demyelination

A failure of autoreactive T cells to undergo apoptosis may contribute to the pathogenesis of multiple sclerosis (MS). The role of the inhibitor of apoptosis (IAP) family of anti-apoptotic proteins such as X-linked IAP (XIAP), human inhibitor of apoptosis-1 (HIAP-1), human inhibitor of apoptosis-2 (H...

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Published in:Multiple sclerosis Vol. 14; no. 5; pp. 577 - 594
Main Authors: Hebb, ALO, Moore, CS, Bhan, V, Campbell, T, Fisk, JD, Robertson, HA, Thorne, M, Lacasse, E, Holcik, M, Gillard, J, Crocker, SJ, Robertson, GS
Format: Journal Article
Language:English
Published: London, England SAGE Publications 01-06-2008
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Abstract A failure of autoreactive T cells to undergo apoptosis may contribute to the pathogenesis of multiple sclerosis (MS). The role of the inhibitor of apoptosis (IAP) family of anti-apoptotic proteins such as X-linked IAP (XIAP), human inhibitor of apoptosis-1 (HIAP-1), human inhibitor of apoptosis-2 (HIAP-2), neuronal apoptosis inhibitory protein (NAIP) and Survivin in relapsing–remitting, secondary-progressive, primary-progressive or benign forms of MS is unclear. We report here that expression of the IAP family of genes in peripheral blood samples and brain tissues from MS cases support a role for differential regulation of these potent anti-apoptotic proteins in the pathology of MS. XIAP mRNA and protein levels were elevated in peripheral blood mononuclear cells from patients with active disease relative to normal subjects. In patients with active MS, HIAP-1 and HIAP-2 mRNA levels were elevated in resting T cells while NAIP mRNA was increased in whole blood. In post-mortem MS brain tissue, XIAP and HIAP-1 in myelin lesions were co-localized with microglia and T cells, respectively. Only in primary-progressive patients was Survivin expression elevated suggestive of a distinct pathological basis for this subtype of MS. Taken together, these results suggest that patterns of inhibitor of apoptosis expression in immune cells may have value in distinguishing between MS subtypes and offer insight into the mechanisms responsible for their distinct clinical courses.
AbstractList A failure of autoreactive T cells to undergo apoptosis may contribute to the pathogenesis of multiple sclerosis (MS). The role of the inhibitor of apoptosis (IAP) family of anti-apoptotic proteins such as X-linked IAP (XIAP), human inhibitor of apoptosis-1 (HIAP-1), human inhibitor of apoptosis-2 (HIAP-2), neuronal apoptosis inhibitory protein (NAIP) and Survivin in relapsing-remitting, secondary-progressive, primary-progressive or benign forms of MS is unclear. We report here that expression of the IAP family of genes in peripheral blood samples and brain tissues from MS cases support a role for differential regulation of these potent anti-apoptotic proteins in the pathology of MS. XIAP mRNA and protein levels were elevated in peripheral blood mononuclear cells from patients with active disease relative to normal subjects. In patients with active MS, HIAP-1 and HIAP-2 mRNA levels were elevated in resting T cells while NAIP mRNA was increased in whole blood. In post-mortem MS brain tissue, XIAP and HIAP-1 in myelin lesions were co-localized with microglia and T cells, respectively. Only in primary-progressive patients was Survivin expression elevated suggestive of a distinct pathological basis for this subtype of MS. Taken together, these results suggest that patterns of inhibitor of apoptosis expression in immune cells may have value in distinguishing between MS subtypes and offer insight into the mechanisms responsible for their distinct clinical courses.
A failure of autoreactive T cells to undergo apoptosis may contribute to the pathogenesis of multiple sclerosis (MS). The role of the inhibitor of apoptosis (IAP) family of anti-apoptotic proteins such as X-linked IAP (XIAP), human inhibitor of apoptosis-1 (HIAP-1), human inhibitor of apoptosis-2 (HIAP-2), neuronal apoptosis inhibitory protein (NAIP) and Survivin in relapsing-remitting, secondary-progressive, primary-progressive or benign forms of MS is unclear. We report here that expression of the IAP family of genes in peripheral blood samples and brain tissues from MS cases support a role for differential regulation of these potent anti-apoptotic proteins in the pathology of MS. XIAP mRNA and protein levels were elevated in peripheral blood mononuclear cells from patients with active disease relative to normal subjects. In patients with active MS, HIAP-1 and HIAP-2 mRNA levels were elevated in resting T cells while NAIP mRNA was increased in whole blood. In post-mortem MS brain tissue, XIAP and HIAP-1 in myelin lesions were co-localized with microglia and T cells, respectively. Only in primary-progressive patients was Survivin expression elevated suggestive of a distinct pathological basis for this subtype of MS. Taken together, these results suggest that patterns of inhibitor of apoptosis expression in immune cells may have value in distinguishing between MS subtypes and offer insight into the mechanisms responsible for their distinct clinical courses. [PUBLICATION ABSTRACT]
Author Robertson, HA
Holcik, M
Moore, CS
Bhan, V
Lacasse, E
Campbell, T
Hebb, ALO
Thorne, M
Crocker, SJ
Fisk, JD
Gillard, J
Robertson, GS
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  organization: Department of Psychiatry, Dalhousie University, Halifax, NS, B3H 2E2, Canada; Department of Psychology, QEII Health Sciences Centre, Halifax, NS, B3H 2E2, Canada
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  organization: Apoptosis Research Centre, Children's Hospital of Eastern Ontario, Ottawa, Ontario, KIH 8L1, Canada
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  fullname: Robertson, GS
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Issue 5
Keywords CD3+ cells
brain
lesions
microglia
demyelination
Autoimmunity
Nervous system diseases
Multiple sclerosis
Neuroglia
Central nervous system
Protein
Inflammatory disease
Encephalon
Microglia
Demyelination
Central nervous system disease
Degenerative disease
Apoptosis
Language English
License CC BY 4.0
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PublicationDate 2008-06-00
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PublicationTitle Multiple sclerosis
PublicationTitleAlternate Mult Scler
PublicationYear 2008
Publisher SAGE Publications
Arnold
Sage Publications Ltd
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atypb9
atypb8
Chofflon M (atypb33) 2005; 19
Feuer R (atypb31) 2003; 163
atypb48
atypb49
atypb44
atypb45
atypb46
atypb47
atypb40
atypb41
atypb42
atypb43
atypb15
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atypb57
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atypb3
atypb53
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atypb19
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atypb27
atypb28
atypb29
atypb22
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atypb37
atypb38
atypb39
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atypb36
atypb73
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atypb71
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Snippet A failure of autoreactive T cells to undergo apoptosis may contribute to the pathogenesis of multiple sclerosis (MS). The role of the inhibitor of apoptosis...
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SubjectTerms Adult
Aged
Autoimmunity - genetics
Autoimmunity - immunology
Baculoviral IAP Repeat-Containing 3 Protein
Biological and medical sciences
Blotting, Western
Brain - pathology
Brain - physiology
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Demyelinating Diseases - genetics
Demyelinating Diseases - immunology
Demyelinating Diseases - pathology
Female
Gene Expression - immunology
Gene Expression Profiling
Humans
Immunologic Factors - genetics
Immunologic Factors - immunology
Inhibitor of Apoptosis Proteins - genetics
Inhibitor of Apoptosis Proteins - immunology
Inhibitor of Apoptosis Proteins - metabolism
Male
Medical sciences
Microglia - immunology
Microtubule-Associated Proteins - genetics
Microtubule-Associated Proteins - immunology
Microtubule-Associated Proteins - metabolism
Middle Aged
Multiple Sclerosis - genetics
Multiple Sclerosis - immunology
Multiple Sclerosis - pathology
Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
Neoplasm Proteins - genetics
Neoplasm Proteins - immunology
Neoplasm Proteins - metabolism
Neurology
Neuronal Apoptosis-Inhibitory Protein - genetics
Neuronal Apoptosis-Inhibitory Protein - immunology
Neuronal Apoptosis-Inhibitory Protein - metabolism
T-Lymphocytes - immunology
T-Lymphocytes - metabolism
Ubiquitin-Protein Ligases
X-Linked Inhibitor of Apoptosis Protein - genetics
X-Linked Inhibitor of Apoptosis Protein - immunology
X-Linked Inhibitor of Apoptosis Protein - metabolism
Title Expression of the inhibitor of apoptosis protein family in multiple sclerosis reveals a potential immunomodulatory role during autoimmune mediated demyelination
URI https://journals.sagepub.com/doi/full/10.1177/1352458507087468
https://www.ncbi.nlm.nih.gov/pubmed/18566024
https://www.proquest.com/docview/218862689
https://search.proquest.com/docview/20823289
https://search.proquest.com/docview/69241479
Volume 14
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