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Med Sci Monit ; 16(1): BR17-23, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20037481

ABSTRACT

BACKGROUND: Recent evidence shows that complements are closely related to the occurrence of choroidal neovascularization (CNV). We studied the effect of complement 5b-9 complex (C5b-9) on membrane permeability and molecular biological behavior in cultured human retinal pigment epithelium (RPE) cells and considered the role of C5b-9 in CNV. MATERIAL/METHODS: Human RPE cells were exposed to different concentrations of C5b-9 for 24 hours, then observed through light and electron microscopy. The dynamics of calcium ion change in cells exposed to sublysis C5b-9 were analyzed by confocal laser scanning microscope, and the amount of VEGF and TGF-beta2 mRNA was determined by reverse transcription polymerase chain reaction (RT-PCR) RESULTS: RPE cells were destroyed when exposed to 80 microg/ml and 40 microg/ml C5b-9. The structure of RPE cells was not obviously changed when exposed to 20 microg/ml or less C5b-9; however, pigment granules are released from the cell membrane when observed using electron microscopy. In most of the cells, calcium fluorescence intensity increased rapidly after the deposition of C5b-9, to a peak at 4 min, lasted for about 6 min, and then began to decrease. The expression of VEGF and TGF- beta2 mRNA in RPE cells with C5b-9 was increased at 4 h and decreased at 24 h, but they were higher than in the control group. CONCLUSIONS: These observations suggest C5b-9 can induce a change in membrane permeability, an increase in cytoplasmic calcium ion concentration, and significant up-regulation of angiogenic factors in cultured RPE cells, which may be one of many potential mechanisms of CNV formation.


Subject(s)
Choroidal Neovascularization/metabolism , Complement C5b/toxicity , Complement C9/toxicity , Multiprotein Complexes/toxicity , Retinal Pigment Epithelium/drug effects , Calcium/metabolism , Cell Membrane Permeability/drug effects , Cells, Cultured , Choroidal Neovascularization/etiology , DNA Primers/genetics , Humans , Microscopy, Confocal , Microscopy, Electron , Multiprotein Complexes/metabolism , Retinal Pigment Epithelium/ultrastructure , Reverse Transcriptase Polymerase Chain Reaction , Transforming Growth Factor beta2/metabolism , Vascular Endothelial Growth Factor A/metabolism
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