Prevention of insulin-dependent diabetes mellitus in non-obese diabetic mice by transgenes encoding modified I-A β-chain or normal I-E α-chain (original) (raw)
- Letter
- Published: 21 June 1990
- Lorraine O'Reilly1,
- Patricia Hutchings1,
- Osami Kanagawa2,
- Elizabeth Simpson3,
- Robert Gravely1,
- Phillip Chandler3,
- Julian Dyson3,
- Jean K. Picard3,
- Andrew Edwards3,
- Dimitris Kioussis4 &
- …
- Anne Cooke1
Nature volume 345, pages 727–729 (1990)Cite this article
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Abstract
INSULIN-dependent diabetes mellitus (IDDM) is a disease with an autoimmune aetiology. The inbred non-obese diabetic (NOD) mouse strain provides a good animal model of the human disease1 and genetic analysis suggests that, as in man, at least one of the several genes controlling the development of IDDM is linked to the major histocompatibility complex2,3. The NOD mouse does not express I-E2 owing to a deletion in the promoter region of the I-E α-chain gene, and the sequence of NOD I-A β-chain in the first external domain is unique with His 56 and Ser 57 (ref. 4) replacing Pro and Asp, respectively, at these positions. There has been considerable interest in the role amino acid 57 might have in conferring susceptibility to autoimmune diseases, including IDDM. The presence of a charged residue (such as Asp) at this position might affect the conformation of the peptide binding groove5. But it could be assumed that Pro 56 gives rise to a different conformation of I-A β-chain than does His 56. We therefore constructed transgenic NOD mice in which the transgene encoded a modified Aβnod with Pro 56, and studied its effect on the development of IDDM in this mouse strain. Previous studies have suggested that NOD mice expressing I-E as a result of the introduction of an I-E α-chain (Eα) transgene are potected from the development of insulitis and hence IDDM6,7. To explore further the protective effect of this molecule we constructed a second class of transgenic NOD mouse carrying an Eαd transgene. Both transgenes protected the mice from IDDM, but this was not associated with a complete deletion of any T cells expressing commonly used T-cell receptor V β genes.
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Authors and Affiliations
- University College and Middlesex School of Medicine, 40-50 Tottenham Street, London, WIP 9PG, UK
Torben Lund, Lorraine O'Reilly, Patricia Hutchings, Robert Gravely & Anne Cooke - Department of Pathology, Washington University, School of Medicine, 660 South Euclid Avenue, St Louis, Missouri, USA
Osami Kanagawa - Clinical Research Centre, Watford Road, Harrow, Middlesex, HA1 3UJ, UK
Elizabeth Simpson, Phillip Chandler, Julian Dyson, Jean K. Picard & Andrew Edwards - National Institute for Medical Research, The Ridgeway, Mill Hill, NW7 1AA, UK
Dimitris Kioussis
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- Torben Lund
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Lund, T., O'Reilly, L., Hutchings, P. et al. Prevention of insulin-dependent diabetes mellitus in non-obese diabetic mice by transgenes encoding modified I-A β-chain or normal I-E α-chain.Nature 345, 727–729 (1990). https://doi.org/10.1038/345727a0
- Received: 25 April 1990
- Accepted: 14 May 1990
- Issue Date: 21 June 1990
- DOI: https://doi.org/10.1038/345727a0