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Publication : Activation of cellular death programs associated with immunosenescence-like phenotype in TPPII knockout mice.

First Author  Huai J Year  2008
Journal  Proc Natl Acad Sci U S A Volume  105
Issue  13 Pages  5177-82
PubMed ID  18362329 Mgi Jnum  J:133572
Mgi Id  MGI:3778855 Doi  10.1073/pnas.0801413105
Citation  Huai J, et al. (2008) Activation of cellular death programs associated with immunosenescence-like phenotype in TPPII knockout mice. Proc Natl Acad Sci U S A 105(13):5177-82
abstractText  The giant cytosolic protease tripeptidyl peptidase II (TPPII) has been implicated in the regulation of proliferation and survival of malignant cells, particularly lymphoma cells. To address its functions in normal cellular and systemic physiology we have generated TPPII-deficient mice. TPPII deficiency activates cell type-specific death programs, including proliferative apoptosis in several T lineage subsets and premature cellular senescence in fibroblasts and CD8(+) T cells. This coincides with up-regulation of p53 and dysregulation of NF-kappaB. Prominent degenerative alterations at the organismic level were a decreased lifespan and symptoms characteristic of immunohematopoietic senescence. These symptoms include accelerated thymic involution, lymphopenia, impaired proliferative T cell responses, extramedullary hematopoiesis, and inflammation. Thus, TPPII is important for maintaining normal cellular and systemic physiology, which may be relevant for potential therapeutic applications of TPPII inhibitors.
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