| First Author | Nakamura-Yanagidaira T | Year | 2011 |
| Journal | Mol Vis | Volume | 17 |
| Pages | 2157-70 | PubMed ID | 21850191 |
| Mgi Jnum | J:179520 | Mgi Id | MGI:5302602 |
| Citation | Nakamura-Yanagidaira T, et al. (2011) Development of spontaneous neuropathy in NF-kappaBp50-deficient mice by calcineurin-signal involving impaired NF-kappaB activation. Mol Vis 17:2157-70 |
| abstractText | PURPOSE: The transcriptional regulator, nuclear factor-kappa B (NF-kappaB)/Rel family are involved in neuronal cell death and survival. Previously, we reported that NF-kappaBp50-deficient (p50-deficient) mice exhibit many features resembling human normal tension glaucoma (NTG). The developmental mechanism of human NTG is not clearly understood, and a radical curative treatment has yet to be established. Our aim is to elucidate the signal cascade which mediates the spontaneous optic neuropathy in p50-deficient mice as a model of NTG. METHODS: To demonstrate the expression and activation of pro-apoptotic factors, which mediate the death of retinal ganglion cells (RGCs) in p50-deficient mice, western blot (WB) and luciferase reporter assays with retinas from p50-deficient and wild type mice, and cultured RGC-5 cells were performed. Furthermore, we tested the neuroprotective effects of chemical reagents (memantine, lomerizine, and tacrolimus) against N-methyl-D-aspartate (NMDA)-susceptible RGC damage according to in vitro experiments with RGC-5 cells. To elucidate the NF-kappaB-mediated death signaling, the effects of chemical reagents on spontaneous optic neuropathy were examined by histopathological studies. RESULTS: WB experiments and luciferase reporter assays showed that NF-kappaB-inducible BCL2-associated X protein (Bax) and a pro-apoptotic factor, activated caspase 3 were expressed in the retina of p50-deficient mice as well as NMDA-treated RGC-5 cells. Further, the constitutively active cleaved forms of calcineurin (CaN), which have been reported to lead to apoptosis, were detected in the retina of p50-deficient mice as well as NMDA-treated RGC-5 cells. Pre-treatment with tacrolimus markedly protected RGC-5 cells from NMDA-induced neurotoxicity, and then both spontaneous RGC death and degenerative changes to the optic nerve in p50-deficient mice were significantly reduced by the chronic administration of tacrolimus. The experiments with cultured RGC-5 cells supported the results of histological examinations with p50-deficient mice, suggesting that CaN activation leads to NF-kappaB-induced Bax activation and caspase 3 activation, and mediates spontaneous optic neuropathy in p50-deficient mice. CONCLUSIONS: Research findings show that the chronic administration of tacrolimus significantly reduces spontaneous optic neuropathy in p50-deficient mice. We demonstrated a potential CaN signal cascade, which spontaneously induces age-dependent RGC death and degenerative optic nerve changes in p50-deficient mice. |
