期刊
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
卷 286, 期 4, 页码 764-770出版社
ACADEMIC PRESS INC
DOI: 10.1006/bbrc.2001.5448
关键词
neurodegenerative disease; nitric oxide; superoxide; reactive nitrogen species; reactive oxygen species; protein kinase C; brain; hippocampus
资金
- NIMH NIH HHS [MH18273, MH1198301] Funding Source: Medline
- NINDS NIH HHS [NS34007] Funding Source: Medline
Protein kinase C (PKC) is an important intracellular signaling molecule whose activity is essential for a number of aspects of neuronal function including synaptic plasticity. We investigated the regulation of PKC activity by reactive nitrogen species in order to examine whether such species regulate PKC in neurons. Neither autonomous nor cofactor-dependent PKC activity was altered when either hippocampal homogenates or rat brain purified PKC were incubated briefly with three different nitric oxide donor compounds. However, brief incubation of either hippocampal homogenates or purified PKC with peroxynitrite (ONOO-) inhibited cofactor-dependent PKC activity in a manner that correlated with the nitration of tyrosine residues on PKC, suggesting that this modification was responsible for the inhibition of PKC. Consistent with this idea, reducing agents had no effect on the inhibition of PKC activity caused by ONOO-. Because there are numerous PKC isoforms that differ in the composition of the regulatory domain, we studied the effect of ONOO- on various PKC isoforms. ONOO- inhibited the cofactor-dependent activity of the alpha, beta II, epsilon, and zeta isoforms, indicating that inhibition of enzymatic activity by ONOO- was not PKC isoform-specific. We also were able to isolate nitrated PKC alpha and PKC beta II from ONOO--treated hippocampal homogenates via immunoprecipitation. Collectively, our findings support the hypothesis that ONOO- inhibits PKC activity via tyrosine nitration in neurons. (C) 2001 Academic Press.
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