Effects of (-)-epigallocatechin gallate on RPE cell migration and adhesion.

Purpose: In diseases such as proliferative vitreoretinopathy (PVR), proliferative diabetic retinopathy (PDR), and age-related macular degeneration (AMD), retinal pigment epithelial (RPE) cells can initiate proliferation and migration and secrete extracellular matrix (ECM) proteins. (-)-Epigallocatechin gallate (EGCG)-a natural anti-oxidant flavonoid that is abundant in green tea-has been shown to suppress the migration and adhesion of many cell types, but its effects on RPE cell migration and adhesion were unknown. Several studies have shown that platelet-derived growth factor (PDGF) enhances proliferation and migration effects on RPE cells in PVR, and that fibronectin is a major ECM component of PVR tissue.

Lycopene inhibits PDGF-BB-induced retinal pigment epithelial cell migration by suppression of PI3K/Akt and MAPK pathways.

Retinal pigment epithelial (RPE) cells play a dominant role in the development of proliferative vitreoretinopathy (PVR), which is the leading cause of failure in retinal reattachment surgery. Several studies have shown that platelet-derived growth factor (PDGF) exhibits chemotaxis and proliferation effects on RPE cells in PVR. In this study, the inhibitory effect of lycopene on PDGF-BB-induced ARPE19 cell migration is examined.

Protective effects of (-)-epigallocatechin gallate on UVA-induced damage in ARPE19 cells.

Purpose: Oxidative injury to the retinal pigment epithelium (RPE) has been proposed to play a contributing role in age-related macular degeneration (AMD). Exposure to solar ultraviolet (UV) radiation is believed to cause the production of reactive oxygen species (ROS), which may cause oxidative damage to RPE cells. Studies have shown that (-)-epigallocatechin gallate (EGCG), an abundant and active component in green tea, can protect several cell types from oxidative stress.

Syntheses, structures, and magnetic properties of mononuclear CuII and tetranuclear CuII3MII (M = Cu, Co, or Mn) compounds derived from N,N'-ethylenebis(3-ethoxysalicylaldimine): cocrystallization due to potential encapsulation of water.

Syntheses, structures, and magnetic properties of one mononuclear inclusion compound [CuIIL1 within (H2O)] (1) and three tetrametal systems of the composition [{CuIIL1}2{CuIIL1MII(H2O)3}]ClO4)2 (M = Cu (2), M = Co (3), M = Mn (4)) derived from the hexadentate Schiff base compartmental ligand N,N'-ethylenebis(3-ethoxysalicylaldimine) (H2L1) have been described. Compounds 1 and 2 crystallize in orthorhombic Pbcn and monoclinic P21/c systems, respectively, and the space group of the isomorphous compounds 3 and 4 is monoclinic C2/c. The water molecule in 1 is encapsulated in the vacant O4 compartment because of the hydrogen bonding interactions with the ether and phenolate oxygens, resulting in the formation of an inclusion product.

Syntheses, structures, and magnetic properties of diphenoxo-bridged M(II)Ln(III) complexes derived from N,N'-ethylenebis(3-ethoxysalicylaldiimine) (M = Cu or Ni; Ln = Ce-Yb): observation of surprisingly strong exchange interactions.

A series of heterodinuclear Cu(II)Ln(III) and Ni(II)Ln(III) complexes, [M(II)L(1)Ln(III)(NO(3))(3)] (M = Cu or Ni; Ln = Ce-Yb), with the hexadentate Schiff base compartmental ligand N,N'-ethylenebis(3-ethoxysalicylaldiimine) (H(2)L(1)) have been synthesized and characterized. The X-ray crystal structure determinations of 13 of these compounds reveal that they are all isostructural. All of these complexes crystallize with the same orthorhombic P2(1)2(1)2(1) space group with closely similar unit cell parameters.

Syntheses, crystal engineering, and magnetic property of a dicyanamide bridged three-dimensional manganese(II)-nitronyl nitroxide coordination polymer derived from a new radical.

Syntheses, structural characterization, crystal engineering, and variable-temperature magnetic study at fixed field strength of a novel dicyanamide bridged three-dimensional manganese(II)-nitronyl nitroxide compound, [Mn(II)(NIT-tz)(dca)(2)] (1), (NIT-tz = 2-(2-thiazole)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazolyl-1-oxy-3-oxide, a new Ullman type radical) have been described. The compound crystallizes in the orthorhombic P2(1)2(1)2(1) space group with the following unit cell parameters: a = 11.015(2) A, b = 12.