Effect of X and Y box deletions on the development of diabetes in H-2Ea chain transgenic NOD mice.
O'Shea, H., Yousaf, N., Altmann, D., Fehervari, Z., Tonks, P., Hetherington, C., Harach, S., Bland, C., Cooke, Anne and Lund, Torben (2006) Effect of X and Y box deletions on the development of diabetes in H-2Ea chain transgenic NOD mice. Scandinavian journal of immunology., 63 (1) . pp. 17-25. ISSN 0300-9475 [Article] (doi:10.1111/j.1365-3083.2006.001701.x)
Abstract
The development of type 1 diabetes in nonobese diabetic (NOD) mice is influenced by major histocompatibility complex (MHC) class II genes. The NOD-E transgenic mouse, which expresses H2-E as a result of the introduction of an Ead gene, is protected from development of type 1 diabetes. While the mechanism of protection remains unclear, the effect has been regarded as a model system for MHC protection from autoimmunity. We have investigated the effect of deletions of the Ea promoter region, which, in turn, affect H2-E expression patterns in transgenic NOD mice. We have constructed transgenic NOD mice where the X (ΔX) and Y (ΔY) boxes of the Ead gene have, respectively, been functionally deleted. Previous reports, using X- or Y-box-deleted H2-E transgenic mice, made by crossing the appropriate transgenes onto the NOD background from C57BL/6 transgenic mice, indicated that promoter mutation abrogated the H2-E-mediated protection seen in NOD-E. The NOD ΔX and NOD ΔY transgenic mice generated in the present study differ in susceptibility to diabetes from wild-type NOD mice. NOD ΔY1 animals are protected from diabetes development, while ΔX mice remain susceptible, albeit to a lesser extent than the parental NOD strain.
Item Type: | Article |
---|---|
Research Areas: | A. > School of Science and Technology > Natural Sciences |
Item ID: | 3977 |
Useful Links: | |
Depositing User: | Mrs Sue Black |
Date Deposited: | 04 Feb 2010 15:59 |
Last Modified: | 13 Oct 2016 14:17 |
URI: | https://eprints.mdx.ac.uk/id/eprint/3977 |
Actions (login required)
![]() |
View Item |
Statistics
Additional statistics are available via IRStats2.