O. Lesur et al., FUNCTIONAL IL-2 RECEPTORS ARE EXPRESSED BY RAT LUNG TYPE-II EPITHELIAL-CELLS, American journal of physiology. Lung cellular and molecular physiology, 17(3), 1997, pp. 495-503
Interferon (IFN)-gamma-induced inhibition of type II epithelial cell t
hymidine incorporation (45% decrease vs. control) was restored by cocu
ltures with mitogen-activated peripheral blood mononuclear cells (PBMC
) and conditioned media (CM) from mitogen-activated PBMC. Successive e
xposure of type II cells to IFN-gamma and interleukin (IL)-2 produced
similar alterations in thymidine incorporation. Given that IL-2 is a p
owerful pleiotropic cytokine produced by lymphoid and myeloid cells, t
he presence of IL-2 receptors (IL-2R) was assessed in primary cultures
of rat type II pneumocytes (TIIP) and the nontransformed alveolar typ
e II epithelial cell line L2. The presence of IL-2R membrane protein o
n rat type II cells was established by immunodetection assays. The exp
ression of all three murine IL-2R alpha-, beta-, and gamma-chain RNA t
ranscripts in primary TIIP cultures and L2 cells was highlighted by re
verse transcriptase-polymerase chain reaction analysis. Overall, these
experiments demonstrate, for the first time, that type II epithelial
cells can express functional IL-2R, confirming TIIP as a potential ''p
artner'' in the lung immune system. Consequently, it can be speculated
that TIIP are new cellular targets for lymphokines using (IL-2R) gamm
a-chain-bearing receptors in lung distal airspaces.