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Monoclonal B-cell h...
Monoclonal B-cell hyperplasia and leukocyte imbalance precede development of B-cell malignancies in uracil-DNA glycosylase deficient mice
- Article/chapterEnglish2005
Publisher, publication year, extent ...
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Elsevier BV,2005
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printrdacarrier
Numbers
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LIBRIS-ID:oai:DiVA.org:umu-57319
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https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-57319URI
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https://doi.org/10.1016/j.dnarep.2005.08.004DOI
Supplementary language notes
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Language:English
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Summary in:English
Part of subdatabase
Classification
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Notes
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Ung-deficient mice have reduced class switch recombination, skewed somatic hypermutation, lymphatic hyperplasia and a 22-fold increased risk of developing B-cell lymphomas. We find that lymphomas are of follicular (FL) and diffuse large B-cell type (DLBCL). All FLs and 75% of the DLBCLs were monoclonal while 25% were biclonal. Monoclonality was also observed in hyperplasia, and could represent an early stage of lymphoma development. Lymphoid hyperplasia occurs very early in otherwise healthy Ung-deficient mice, observed as a significant increase of splenic B-cells. Furthermore, loss of Ung also causes a significant reduction of T-helper cells, and 50% of the young Ung(-/-) mice investigated have no detectable NK/NKT-cell population in their spleen. The immunological imbalance is confirmed in experiments with spleen cells where the production of the cytokines interferon gamma, interleukin 6 and interleukin 2 is clearly different in wild type and in Ung-deficient mice. This suggests that Ung-proteins, directly or indirectly, have important functions in the immune system, not only in the process of antibody maturation, but also for production and functions of immunologically important cell types. The immunological imbalances shown here in the Ung-deficient mice may be central in the development of lymphomas in a background of generalised lymphoid hyperplasia.
Subject headings and genre
Added entries (persons, corporate bodies, meetings, titles ...)
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Ericsson, MadeleneDepartment of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim(Swepub:umu)maer0239
(author)
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Dai, Hong Yan
(author)
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Peña-Diaz, Javier
(author)
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Slupphaug, Geir
(author)
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Nilsen, Hilde
(author)
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Aarset, Harald
(author)
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Krokan, Hans E
(author)
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Department of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim
(creator_code:org_t)
Related titles
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In:DNA Repair: Elsevier BV4:12, s. 1432-14411568-78641568-7856
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