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J. Biochem, 2003, Vol. 133, No. 4 501-505
© 2003 Japanese Biochemical Society

CELL

Nitric Oxide Synthase Induction, cGMP Elevation, and Biopterin Synthesis in Vascular Smooth Muscle Cells Stimulated with Interleukin-1ß in Hypoxia

Kaori Nagao1, Shigeo Takenaka2, Ryoichi Yamaji1, Hiroshi Inui+,1 and Yoshihisa Nakano1

1 Department of Applied Biological Chemistry, and 2 Department of Veterinary Sciences, Osaka Prefecture University, Sakai, Osaka 599-8531

In cultured rat vascular smooth muscle cells (VSMC), inducible nitric oxide synthase (iNOS) expression evoked by interleukin-1ß (IL-1ß) or tumor necrosis factor–{alpha} was greatly enhanced in hypoxia (2% O2), compared to in normoxia. In contrast, iNOS induction by interferon-{gamma}, lipopolysaccharide or their combination was barely influenced by hypoxia. These results indicate that iNOS induction is regulated by hypoxia in different manners, depending on the stimuli in VSMC. Nitric oxide (NO) production in response to stimulation with interferon-{gamma} plus lipopolysaccharide was significantly decreased in hypoxia, due to a decrease in the concentration of O2 as a substrate. In contrast, the level of NO production in hypoxia was almost the same as that in normoxia when the cells were stimulated by IL-1ß. In addition, cGMP increased in response to IL-1ß in hypoxia to a level comparable to that in normoxia. Thus, it seems that the IL-1ß–induced expression of iNOS is up-regulated in hypoxia to compensate for a decrease in the enzyme activity due to the lower availability of O2 as a substrate, and consequently a sufficient amount of NO is produced to elevate cGMP to an adequate level. In addition, the IL-1ß–induced synthesis of tetrahydrobiopterin, a cofactor for iNOS, was also greatly stimulated by hypoxia in VSMC.

+ To whom correspondence should be addressed. Tel/Fax: +81-72-254-9454, Email: inui{at}server.biochem.osakafu-u.ac.jp


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