Differential tumor necrosis factor and nitric oxide production in retinal Müller glial cells from C3H/HeN and C3H/HeJ mice

Abstract

Tumor necrosis factor (TNF) and nitric oxide (NO) have been shown to play a role in the pathogenesis of endotoxin-induced uveitis (EIU) in rats. Susceptibility to develop EIU in vivo is correlated with the extent of TNF production by retinal Müller glial cells (RMG). Moreover, RMG cells from the susceptible Lewis rat strain synthesize high amounts of nitrite under in vitro stimulation. Variations in susceptibility to endotoxin are observed among mice strains: C₃H/HeN mice are known to be susceptible to develop EIU while C₃H/HeJ are refractory. We show here that treatment of RMG cells from both strains with LPS+IFN-γ does not induce TNF synthesis in culture supernatants but produces high amounts of NO only in the supernatants from activated C₃H/HeN RMG cells. The addition of TNF in the culture medium containing LPS/IFN-γ further increases nitrite production in C₃H/HeN RMG cells and allows the synthesis of low levels of nitrite in C₃H/HeJ RMG cells. Addition of a specific NO synthase inhibitor, N^G-monomethyl-L-arginine (L-NMMA), blocks NO release. We have previously shown that intraperitoneal injections of the NO synthase inhibitor, N^G-nitro-L-arginine methyl ester (L-NAME) which inhibited nitrite and TNF release in the ocular media reduced EIU in rat. We conclude here that the in vivo susceptibility to develop EIU in mice is correlated with the extent of in vitro nitrite production by RMG cells confirming the implication of NO in the induction of ocular inflammation. The low level of retinal inflammation observed during EIU in C₃H/HeN mice compared to rats could be related to the absence of TNF production by RMG cells.

Key Words:

• Mouse
• Müller glial cell
• tumor necrosis factor
• nitric oxide synthase
• culture
• susceptibility