Kaneko Shiho, Okuda-Ashitaka Emiko, Ando Akira, Nishimura Kazuhiro, Igarashi Kazuei, Maeda Masahide, Furuta Kyoji, Suzuki Masaaki, Matsumura Miyo, Ito Seiji
Department of Ophthalmology, Kansai Medical University, Moriguchi, Osaka, Japan.
Am J Physiol Cell Physiol. 2007 Aug;293(2):C729-37. doi: 10.1152/ajpcell.00018.2007. Epub 2007 May 9.
We previously showed that ornithine was mainly transported via cationic amino acid transporter (CAT)-1 in human retinal pigment epithelial (RPE) cell line, human telomerase RT (hTERT)-RPE, and that CAT-1 was involved in ornithine cytotoxicity in ornithine-delta-aminotransferase (OAT)-deficient cell produced by a OAT specific inhibitor, 5-fluoromethylornithine (5-FMO). We showed here that CAT-1 mRNA expression was increased by ornithne in OAT-deficient RPE cells, which was reversed by an inhibitor of ornithine decarboxylase (ODC), alpha-difluoromethylornithine (DFMO). Polyamines, especially spermine, one of the metabolites of ODC, also enhanced the expression of CAT-1 mRNA. ODC mRNA expression was also increased by ornithine and polyamines, and gene silencing of ODC by siRNA decreased ornithine transport activity and its cytotoxicity. In addition, the mRNA of nuclear protein c-myc was also increased in 5-FMO- and ornithine-treated hTERT-RPE cells, and gene silencing of c-myc prevented the induction of CAT-1 and ODC. Increases in expression of CAT-1, ODC, and c-myc, and the inhibition of these stimulated expression by DFMO were also observed in primary porcine RPE cells. These results suggest that spermine plays an important role in stimulation of mRNA expression of CAT-1, which is a crucial role in ornithine cytotoxicity in OAT-deficient hTERT-RPE cells.
我们之前发现,在人视网膜色素上皮(RPE)细胞系人端粒酶逆转录酶(hTERT)-RPE中,鸟氨酸主要通过阳离子氨基酸转运体(CAT)-1进行转运,并且在鸟氨酸δ-氨基转移酶(OAT)特异性抑制剂5-氟甲基鸟氨酸(5-FMO)产生的OAT缺陷细胞中,CAT-1参与了鸟氨酸的细胞毒性作用。我们在此表明,在OAT缺陷的RPE细胞中,鸟氨酸可增加CAT-1 mRNA的表达,而鸟氨酸脱羧酶(ODC)抑制剂α-二氟甲基鸟氨酸(DFMO)可使其逆转。多胺,尤其是ODC的代谢产物之一精胺,也能增强CAT-1 mRNA的表达。鸟氨酸和多胺也能增加ODC mRNA的表达,通过小干扰RNA(siRNA)使ODC基因沉默可降低鸟氨酸转运活性及其细胞毒性。此外,在5-FMO和鸟氨酸处理的hTERT-RPE细胞中,核蛋白c-myc的mRNA也增加,c-myc基因沉默可阻止CAT-1和ODC的诱导。在原代猪RPE细胞中也观察到CAT-1、ODC和c-myc表达的增加,以及DFMO对这些刺激表达的抑制作用。这些结果表明,精胺在刺激CAT-1 mRNA表达中起重要作用,这在OAT缺陷的hTERT-RPE细胞中鸟氨酸的细胞毒性中起关键作用。