NITRIC-OXIDE AND PEROXYNITRITE-DEPENDENT ACONITASE INACTIVATION AND IRON-REGULATORY PROTEIN-1 ACTIVATION IN MAMMALIAN FIBROBLASTS

The reaction of reactive oxygen and nitrogen species with the [4Fe-4S] (2+) cluster of mitochondrial (m-) and cytosolic (c-) aconitases leads to loss of catalytic activity and, in the case of the c-aconitase, tr iggers total cluster disruption to yield the iron-regulatory protein-1 (IRP-1). Herein we have studied the relative contribution and interpl ay of reactive oxygen species (O-2(radical anion) and H2O2), nitric ox ide ((NO)-N-.), and peroxynitrite in the modulation of m- and c-aconit ase and IRP-1 activities in V79-M8 mammalian fibroblasts, identifying key variables that control the various reactivities at the cellular le vel. Extracellular production of H2O2 led to inactivation of both m- a nd c-aconitase and IRP-1 activation, while extracellular O-2(radical a nion) had no effect. However, increased intracellular production of OH caused a loss in m- and c-aconitase activity and IRP-1 activation. Ni tric oxide released from NOC-12 had a more complex effect on aconitase and IRP-1 activities. Mitochondrial aconitase was more sensitive than c-aconitase to (NO)-N-.-mediated inactivation and minimal activation of IRP-1 was observed during a 30-min exposure to the (NO)-N-. donor. The action of (NO)-N-. was down- or upregulated by the presence of ext ra- or intracelular O-2(radical anion), respectively. Extracellular O- 2(radical anion) decreased the (NO)-N-.-mediated inactivation of aconi tases, due to the preferential extracellular decomposition and the low er diffusivity of peroxynitrite compared to (NO)-N-.. On the other han d,(NO)-N-. exposure concomitant with enhanced intracellular O-2(radica l anion), fluxes lead to intracellular peroxynitrite formation as evid enced by Western blot analysis of nitrated proteins, which increased t he effects observed with (NO)-N-. alone. Peroxynitrite-mediated aconit ase inactivation, IRP-1 activation, and cellular protein nitration wer e more pronounced in cells with low GSH content such as V79-M8 glutath ione-depleted cells as well as in pGSOD4 cells which contain 32% of th e GSH of the parental strain. Mechanistically, our results imply that the differential actions of the studied reactive species toward cellul ar aconitases depend on at least three critical factors: (i) their rea ction rates with aconitases, (ii) the cellular compartment where they are formed, and (iii) the intracellular status of glutathione. (C) 199 8 Academic Press.