Journal
JOURNAL OF IMMUNOLOGY
Volume 187, Issue 4, Pages 1542-1546Publisher
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1100907
Keywords
-
Categories
Funding
- National Institutes of Health [AI 019335, AI 079159]
- Howard Hughes Medical Institute
Ask authors/readers for more resources
The molecular mechanisms that regulate mature T cell fate and enable cells to differentiate into memory T cells are largely unknown. Memory T cells share certain key features with stem cells: they both have the ability to self-renew and are long-lived. The Wnt-beta-catenin signaling pathway is a key player in regulating stem cell self-renewal and differentiation. We generated a conditional knockout mouse that specifically lacks beta-catenin in mature T cells and report in this article that beta-catenin is not involved in regulating effector versus memory T cell differentiation. beta-catenin-deficient memory T cells were phenotypically and functionally indistinguishable from control cells and made normal recall responses. beta-catenin deficiency does not affect T cell migration, T cell function in a model of chronic infection, or lymphopenia-induced proliferation. Together, our data suggest that self-renewal and differentiation are regulated differently in memory T cells compared with epithelial and hematopoietic stem cells. The Journal of Immunology, 2011, 187: 1542-1546.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available