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Evidence for Involvement of p59fyn in Fasting‐Induced Thymic Involution
Author(s) -
Nishio H.,
Takase I.,
Fukunishi S.,
Takagi T.,
Tamura A.,
Miyazaki T.,
Suzuki K.
Publication year - 2005
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.2005.01646.x
Subject(s) - medicine , fyn , endocrinology , involution (esoterism) , thymic involution , cd8 , biology , thymocyte , kinase , terminal deoxynucleotidyl transferase , tyrosine kinase , t cell , immunology , immune system , microbiology and biotechnology , immunohistochemistry , receptor , tunel assay , consciousness , neuroscience
p59fyn, a member of the src‐family protein tyrosine kinase, is expressed abundantly in thymus. We examined the possible involvement of p59fyn in thymic involution induced by a fasting stress in Fyn –/– mice. An acute 48 h fast resulted in severe atrophy of the thymus and a marked decrease of the total thymocyte number with depletion of the CD4 + CD8 + [double positive (DP)] population in Fyn +/+ (control) mice. A remarkable increase in terminal deoxynucleotidyl transferase‐mediated dUTP‐biotin nick end labelling‐positive signals was detected in the fasted group of control mice. However, these findings were not observed in Fyn –/– mice. Interestingly, MRL/MPJ‐lpr/lpr, a Fas‐deficient model animal, also showed no significant decrease of DP cell numbers in the fasted group. p59fyn is known to interact with Fas signalling, and these findings suggest that p59fyn is involved in fasting‐induced thymic involution, raising the possibility that Fas/p59fyn‐mediated signalling may, at least partially, be associated with the phenomenon.