The hairless (hr) gene is expressed in a large number of tissues, primarily
the skin, and a mutation in the hi gene is responsible for the typical cut
aneous phenotype of hairless mice. R;Mutant hr mouse strains show immune de
fects involving especially T cells and macrophages, as well as an age-relat
ed immunodeficiency and an accelerated atrophy of the thymus. These data su
ggest that the hr mutation causes a defect of this organ. although hr trans
cripts have not been detected in fetal or adult mice thymus. The present st
udy analyses the thymus of young (3 mo) and adult (9 mo) homozygous hr-rh-j
mice (a strain of hairless mice) by means of structural techniques and imm
unohistochemistry to selectively identify thymic epithelial cells, dendriti
c cells, and macrophages. There were structural alterations in the thymus o
f both young and adult rh-rh-j mice, which were more severe in older animal
s. These alterations consisted of relative cortical atrophy, enlargement of
blood vessels, proliferation of perivascular connective tissue, and the ap
pearance of cysts. hr-rh-j mice also showed a decrease in the number of epi
thelial and dendritic cells, and macrophages. Taken together, present resul
ts strongly suggest degeneration and accelerated age-dependent regression o
f the thymus in hr-rh-j mice, which could explain at least in part the immu
ne defects reported in hairless mouse strains.