| Literature DB >> 22365666 |
Ineke den Braber1, Tendai Mugwagwa, Nienke Vrisekoop, Liset Westera, Ramona Mögling, Anne Bregje de Boer, Neeltje Willems, Elise H R Schrijver, Gerrit Spierenburg, Koos Gaiser, Erik Mul, Sigrid A Otto, An F C Ruiter, Mariette T Ackermans, Frank Miedema, José A M Borghans, Rob J de Boer, Kiki Tesselaar.
Abstract
Parallels between T cell kinetics in mice and men have fueled the idea that a young mouse is a good model system for a young human, and an old mouse, for an elderly human. By combining in vivo kinetic labeling using deuterated water, thymectomy experiments, analysis of T cell receptor excision circles and CD31 expression, and mathematical modeling, we have quantified the contribution of thymus output and peripheral naive T cell division to the maintenance of T cells in mice and men. Aging affected naive T cell maintenance fundamentally differently in mice and men. Whereas the naive T cell pool in mice was almost exclusively sustained by thymus output throughout their lifetime, the maintenance of the adult human naive T cell pool occurred almost exclusively through peripheral T cell division. These findings put constraints on the extrapolation of insights into T cell dynamics from mouse to man and vice versa. Copyright ÂEntities:
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Year: 2012 PMID: 22365666 DOI: 10.1016/j.immuni.2012.02.006
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745