Inability of rat alveolar macrophages to recycle L-citrulline to L-arginine despite induction of argininosuccinate synthetase mRNA and protein, and inhibition of nitric oxide synthesis by exogenous L-citrulline
R. Hammermann et al., Inability of rat alveolar macrophages to recycle L-citrulline to L-arginine despite induction of argininosuccinate synthetase mRNA and protein, and inhibition of nitric oxide synthesis by exogenous L-citrulline, N-S ARCH PH, 358(6), 1998, pp. 601-607
In the present study it was tested whether rat alveolar macrophages (AM Phi
) convert L-citrulline to L-arginine to maintain nitric oxide (NO) synthesi
s under conditions of limited availability of L-arginine. Rat AM Phi (0.5 x
10(6) cells/well, cultured for 20 h in the absence or presence of 1 mu g/m
l lipopolysaccharides, LPS), were incubated for 6 h in amino acid-free Kreb
s solution and nitrite accumulation was determined as a measure of NO synth
esis. After culture in the absence of LPS, nitrite in the incubation media
was at the detection limit, independent of the addition of L-arginine or L-
citrulline. AM Phi, cultured in the presence of LPS, produced about 4 nmol
per 106 cells and 6 h nitrite, and L-arginine enhanced nitrite accumulation
in a concentration-dependent manner, maximally about threefold (EC50: 55 m
u M). In LPS-treated AM Phi L-citrulline (up to 10 mM) failed to enhance ni
trite accumulation, but rather inhibited it by about 50% in the presence of
100 mu M L-arginine, i.e. when NO synthesis was enhanced. L-Arginine in th
e culture medium was H-3-labelled and its metabolism analysed by HPLC. In m
edium of AM Phi exposed to LPS [H-3]-L-arginine was reduced by about 60% af
ter a 20-h culture period and this was almost balanced by an almost equal i
ncrease in [H-3]-L-citrulline and [H-3]-L-ornithine, i.e. L-arginine was ma
rkedly consumed. When [C-14]-L-citrulline was added to the culture medium o
f AM Phi, no significant formation of [C-14]-L-arginine could be detected.
On the other hand, argininosuccinate synthetase mRNA (by RT-PCR) and protei
n (by Western blot) was marginally detectable in control AM Phi, but clearl
y induced after exposure to LPS. Finally, L-citrulline was shown to inhibit
L-arginine uptake in a concentration dependent manner, by about 50% at 10
mM.
In conclusion, although the expression of argininosuccinate synthetase in r
at AM Phi can be induced by LPS, AM Phi appear not to be able to recycle si
gnificant amounts of L-citrulline to L-arginine to maintain sustained NO sy
nthesis. On the contrary, at high concentrations L-citrulline can reduce NO
synthesis, and this effect appears to be caused by inhibitory effects on L
-arginine uptake.