K. Arsalane et al., Increased serum and urinary concentrations of lung Clara cell protein in rats acutely exposed to ozone, TOX APPL PH, 159(3), 1999, pp. 169-174
Clara cell protein (CC16) is a 16-17-kDa protein secreted by Clara cells in
the bronchial lining fluid of the lung from which it passively diffuses in
to serum before being eliminated by the kidneys. The concentration of CC16
in serum has recently been proposed as a peripheral marker of the integrity
of Clara cells and/or of the bronchoalveolar/blood barrier. To evaluate th
e sensitivity of this new lung marker to acute epithelial damage induced by
ozone (O-3), CC16 was determined in the serum of rats after a single 3-h e
xposure to 0.3, 0.6, or 1 ppm O-3. The urinary excretion of the protein was
also studied in rats repeatedly exposed to 1 ppm O-3, 3 h/day, for up to 1
0 days. The concentrations of CC16 in the lung or trachea homogenates, the
lung CC16 mRNA levels, and classical markers of lung injury in bronchoalveo
lar lavage fluid (BALF) were also determined. O-3 produced a transient incr
ease of CC16 concentration in serum that reached values on average 13 times
above normal 2 h after exposure to 1 ppm O-3 The intravascular leakage of
CC16 was dose-dependent and correlated with the extent of lung injury as as
sessed by the levels of total protein, LDH, and inflammatory cells in BALE.
This effect was most likely responsible for the concomitant marked reducti
on of CC16 concentrations in BALE and lung homogenate, since the CC16 mRNA
levels in the lungs were unchanged and the absolute amounts of CC16 leaking
into serum or lost from the respiratory tract were similar. These changes
were paralleled by an elevation of the urinary excretion of CC16 resulting
from an overloading of the tubular reabsorption process. These results demo
nstrate that the assay of CC16 in serum and even in urine represents a new
noninvasive test to detect the increased lung epithelial permeability induc
ed by O-3. (C) 1999 Academic Press.