Lymphocytes in the bronchoalveolar lavage fluid (BAL) are increased in many
lung diseases, which might be an indicator for protective reactions or pat
hology. High er lymphocyte numbers at distinct organ sites may be due to a
number of reasons such as increased entry, increased proliferation, reduced
apoptosis or reduced exit. It is not known whether lymphocyte numbers are
influenced by local proliferation in the healthy lung. Therefore, the proli
feration of lymphocytes was studied in vivo in different lung compartments
of healthy rats: the marginal vascular pool, the interstitial pool and the
bronchoalveolar pool. Bromodeoxyuridine (BrdU) was used as an S-phase proli
feration marker. The cells were obtained 1 h and 24 h after i.v. injection
of BrdU. The labeled cells and their phenotypes were determined by immunocy
tochemistry, since it was not possible to use flow cytometry because of the
low numbers. In the lung compartments 0.7-1.5% of all nucleated cells were
found to be BrdU(+), whereas 24 h later this increased to 3.2-5.7%. The fr
equency of BrdU(+) T cells was significantly higher in the lung compartment
s compared to the blood, with the maximum in the marginal vascular pool. Lo
cal proliferation of lymphocytes involved mainly CD8(+) T cells, Thus. loca
l proliferation plays a role in the number and composition of lymphocytes i
n the healthy normal lung.