Gastrointestinal epithelium is an early extrathymic site for increased prevalence of CD34(+) progenitor cells in contrast to the thymus during primary simian immunodeficiency virus infection
Jj. Mattapallil et al., Gastrointestinal epithelium is an early extrathymic site for increased prevalence of CD34(+) progenitor cells in contrast to the thymus during primary simian immunodeficiency virus infection, J VIROLOGY, 73(5), 1999, pp. 4518-4523
The objective of this study was to determine the effects of primary simian
immunodeficiency virus (SIV) infection on the prevalence and phenotype of p
rogenitor cells present in the gastrointestinal epithelia of SIV-infected r
hesus macaques, a primate model for human immunodeficiency virus pathogenes
is, The gastrointestinal epithelium was residence to progenitor cells expre
ssing CD34 antigen, a subset of which also coexpressed Thy-1 and c-kit rece
ptors, suggesting that the CD34(+) population in the intestine comprised a
subpopulation of primitive precursors, Following experimental SIVmac251 inf
ection, an ear ly increase in the proportions of CD34(+) Thy-1(+) and CD34(
+) c-kit(+) progenitor cells was observed in the gastrointestinal epitheliu
m, Tn contrast, the proportion of CD34(+) tells in the thymus declined duri
ng primary SIV infection, which was characterized by a decrease in the freq
uency of CD34(+) Thy-1(+) progenitor cells. A severe depletion in the frequ
ency of CD4-committed CD34(+) progenitors was observed in the gastrointesti
nal epithelium 2 weeks after SIV infection which persisted even 4 weeks aft
er infection. A coincident increase in the frequency of CD8-committed CD34(
+) progenitor cells was observed during primary SIV infection. These result
s indicate that in contrast to the primary lymphoid organs such as the thym
us, the gastrointestinal epithelium may be an early extrathymic site for th
e increased prevalence of both primitive and committed CD34(+) progenitor c
ells. The gastrointestinal epithelium may potentially play an important rol
e in maintaining T-cell homeostasis in the intestinal mucosa during primary
SIV infection.