Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Invest Ophthalmol Vis Sci. 2010 Nov;51(11):5617-22. doi: 10.1167/iovs.10-5463. Epub 2010 Jun 10.
ABCG2 is a putative marker of progenitor cells, including the corneal epithelium. The authors investigated whether ABCG2 functions in the homeostasis of corneal epithelial cells using abcg2 knockout (KO) mice and corneal epithelial cell lines.
abcg2 KO mice and a spontaneously immortalized murine corneal epithelial cell line (TKE2) were used for experiments. Flow cytometry was used to determine the presence of side population (SP) cells based on the ability of ABCG2 to efflux Hoechst 33342 dye. Expression of ABCG2 was also examined by RT-PCR. Cytotoxicity assay (IC(50)) and propidium iodide staining were performed in semiconfluent cells treated with hypoxia (1% O(2)) or with the pro-oxidant mitoxantrone.
abcg2 KO mice had a normal corneal epithelial phenotype; however, cultured abcg2 KO epithelial cells were prone to oxidative damage by mitoxantrone. TKE2 cells were resistant to mitoxantrone at low doses, but higher concentrations were toxic in a dose-dependent manner. Coculture with the ABCG2 inhibitors reserpine and Ko143 inhibited resistance to mitoxantrone, with a statistically higher cell death ratio. abcg2 KO cells were also significantly more sensitive to hypoxia than were wild-type control cells.
ABCG2 may protect corneal epithelial progenitor SP cells against oxidative stress induced by toxins and hypoxia.
ABCG2 是祖细胞的一个假定标志物,包括角膜上皮细胞。作者使用 abcg2 敲除 (KO) 小鼠和角膜上皮细胞系来研究 ABCG2 是否在角膜上皮细胞的稳态中发挥作用。
使用 abcg2 KO 小鼠和自发永生化的小鼠角膜上皮细胞系 (TKE2) 进行实验。流式细胞术用于根据 ABCG2 将 Hoechst 33342 染料外排的能力来确定侧群 (SP) 细胞的存在。还通过 RT-PCR 检查 ABCG2 的表达。在接受缺氧 (1% O2) 或促氧化剂米托蒽醌处理的半汇合细胞中进行细胞毒性测定 (IC50) 和碘化丙啶染色。
abcg2 KO 小鼠具有正常的角膜上皮表型;然而,培养的 abcg2 KO 上皮细胞容易受到米托蒽醌的氧化损伤。TKE2 细胞对低剂量的米托蒽醌具有抗性,但高浓度则以剂量依赖性方式产生毒性。与 ABCG2 抑制剂利血平和 Ko143 共培养抑制了对米托蒽醌的抗性,细胞死亡率有统计学上的显著增加。与野生型对照细胞相比,abcg2 KO 细胞对缺氧也更为敏感。
ABCG2 可能保护角膜上皮祖细胞 SP 细胞免受毒素和缺氧引起的氧化应激。