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As a featured ocular inflammatory disease, autoimmune uveitis is the major cause of blindness in the clinic. Although current immunosuppressive regimens can alleviate the progression of autoimmune uveitis, they have serious side effects. Therefore, an alternative therapeutic strategy is urgently required. The present study investigated the therapeutic efficacy of human amniotic epithelial cells (hAECs) on autoimmune uveitis in a rat model. Herein, experimental autoimmune uveitis (EAU) was induced in rats via a subcutaneous injection of interphotoreceptor retinoid-binding protein. EAU rats were treated with hAECs or the vehicle solution via a subretinal injection on day 0 and day 6 after immunization, and rats were sacrificed on day 12 and day 18 for further analysis. The pathological development of EAU was evaluated by slit lamp microscopy. Immune cell infiltration and retinal structure damage were examined by histological examination of hematoxylin and eosin (H&E) and immunofluorescence staining. T-cell subsets were detected by flow cytometry, and the levels of inflammatory cytokines were quantified by enzyme-linked immunosorbent assay (ELISA). hAEC treatment ameliorated the pathological progression of EAU and preserved the retinal structure organization and thickness, especially in the preventive group that received a subretinal injection on day 0. Moreover, hAECs inhibited the retinal infiltration of macrophages and T-cells. Mechanistically, hAECs modulated the balance of T-cell subsets by downregulating T helper (Th)17 cells and upregulating T regulatory (Treg) cells, as confirmed by decreased interleukin (IL)-17 and increased IL-10 levels in the spleens and lymph nodes of EAU rats. Furthermore, hAECs improved the local cytokine environment in EAU rats by suppressing the monocyte chemoattractant protein (MCP)-1, IL-17 and interferon (IFN)-γ levels and enhancing the IL-10 in the aqueous humor. Therefore, subretinal transplantation of hAECs in EAU rats ameliorated ocular inflammation, preserved the retinal structure and coordinated the immune balance. The current study provides a novel therapeutic strategy for autoimmune uveitis and related ocular inflammatory diseases in the clinic.

Magnesioferrite, a rare metasomatic mineral, was discovered for the first time in China from the Qinlou Au (Fe, Cu) magnesian skarn deposit, Sanpu, Huaibei, Auhui Province, and the Mulonggou Fe (Mo, Cu) magnesian skarn deposit, Luonan County, Shaanxi Province. In this paper, the geological setting, mineral associations, chemical composition, some physical properties, X-ray powder diffraction data and infrared spectroscopy of magnesioferrite and magnesiomagnetite are discussed. Magnesioferrite contains 17.66%–13.48% of MgO. Its main associated minerals are clinohumite, chondrodite, serpentine, calcite and magnesiomagnetite. The density of magnesioferrite is 4.537–4.720, reflectances in percent are: 17.8–18.1, hardness is 838–900 kg/mm2, and the cell parameter ao = 8.371–8.379 A. A systematic study of the magnesioferrite-magnesiomagnetite-magnetite series suggests that along with the increase of magnesioferrite molecules in the mineral, the density, reflectances and cell parameters decrease correspondingly, the hardness heightens, and the infrared absorption spectral band becomes wider. The authors consider that magnesioferrite is a product of contact metasomatism between hypabyssal intermediate-acid intrusions and dolomitic marble. It was formed in shallow exocontact zones under relatively oxidized conditions.

Minerals of various mantle-derived xenoliths from the Hannuoba basalt in Hebei Province have been studied by means of IR spectroscopy. The results show that all xenoliths from the mantle at depths