The Influence of the Proinflammatory Cytokine, Osteopontin, on Autoimmune Demyelinating Disease

Author:

Chabas Dorothée1,Baranzini Sergio E.2,Mitchell Dennis1,Bernard Claude C. A.3,Rittling Susan R.4,Denhardt David T.4,Sobel Raymond A.5,Lock Christopher1,Karpuj Marcela12,Pedotti Rosetta1,Heller Renu6,Oksenberg Jorge R.2,Steinman Lawrence1

Affiliation:

1. Department of Neurology and Neurological Sciences, Beckman Center for Molecular Medicine, B002, Stanford, CA 94305, USA.

2. Department of Neurology, University of California at San Francisco School of Medicine, San Francisco, CA 94143, USA.

3. Neuroimmunology Laboratory, Department of Biochemistry, La Trobe University, Bundoora, Victoria, 3083 Australia.

4. Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.

5. Department of Pathology (Neuropathology), Stanford University School of Medicine, Stanford, CA 94305, USA.

6. Roche Bioscience, 3401 Hillview Avenue, Palo Alto, CA 94304, USA.

Abstract

Multiple sclerosis is a demyelinating disease, characterized by inflammation in the brain and spinal cord, possibly due to autoimmunity. Large-scale sequencing of cDNA libraries, derived from plaques dissected from brains of patients with multiple sclerosis (MS), indicated an abundance of transcripts for osteopontin (OPN). Microarray analysis of spinal cords from rats paralyzed by experimental autoimmune encephalomyelitis (EAE), a model of MS, also revealed increased OPN transcripts. Osteopontin-deficient mice were resistant to progressive EAE and had frequent remissions, and myelin-reactive T cells in OPN –/– mice produced more interleukin 10 and less interferon-γ than in OPN +/+ mice. Osteopontin thus appears to regulate T helper cell–1 (T H 1)–mediated demyelinating disease, and it may offer a potential target in blocking development of progressive MS.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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