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 |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: ALO surname: Hebb fullname: Hebb, ALO organization: Department of Pharmacology, Dalhousie University, Halifax, NS, B3H 1X5, Canada – sequence: 2 givenname: CS surname: Moore fullname: Moore, CS organization: Department of Pharmacology, Dalhousie University, Halifax, NS, B3H 1X5, Canada – sequence: 3 givenname: V surname: Bhan fullname: Bhan, V organization: Department of Medicine (Neurology), Dalhousie University, Halifax, NS, B3H 1V7, Canada – sequence: 4 givenname: T surname: Campbell fullname: Campbell, T organization: Department of Medicine (Neurology), Dalhousie University, Halifax, NS, B3H 1V7, Canada – sequence: 5 givenname: JD surname: Fisk fullname: Fisk, JD organization: Department of Psychiatry, Dalhousie University, Halifax, NS, B3H 2E2, Canada; Department of Psychology, QEII Health Sciences Centre, Halifax, NS, B3H 2E2, Canada – sequence: 6 givenname: HA surname: Robertson fullname: Robertson, HA organization: Department of Pharmacology, Dalhousie University, Halifax, NS, B3H 1X5, Canada – sequence: 7 givenname: M surname: Thorne fullname: Thorne, M organization: Department of Pharmacology, Dalhousie University, Halifax, NS, B3H 1X5, Canada – sequence: 8 givenname: E surname: Lacasse fullname: Lacasse, E organization: Aegera Therapeutics Inc., Nun’s Island (Montreal), PQ, H3E 1A8, Canada – sequence: 9 givenname: M surname: Holcik fullname: Holcik, M organization: Apoptosis Research Centre, Children's Hospital of Eastern Ontario, Ottawa, Ontario, KIH 8L1, Canada – sequence: 10 givenname: J surname: Gillard fullname: Gillard, J organization: Aegera Therapeutics Inc., Nun’s Island (Montreal), PQ, H3E 1A8, Canada – sequence: 11 givenname: SJ surname: Crocker fullname: Crocker, SJ organization: Molecular and Integrative Neuroscience Department, the Scripps Research Institute, La Jolla, CA, 92037, USA – sequence: 12 givenname: GS surname: Robertson fullname: Robertson, GS organization: Department of Pharmacology, Dalhousie University, Halifax, NS, B3H 1X5, Canada; Department of Psychiatry, Dalhousie University, Halifax, NS, B3H 2E2, Canada |
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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 |
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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 |
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