1.Cl- channel expression in choroid plexus epithelial cells.
Peter D BROWN ; Hidetoshi KAJITA ; Aneela MAJID ; Tracey SPEAKE
Journal of Korean Medical Science 2000;15(Suppl):S10-S11
No abstract available.
Animal
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Chloride Channels/metabolism
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Chloride Channels/biosynthesis*
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Choroid Plexus/metabolism*
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Choroid Plexus/cytology
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Epithelial Cells/metabolism*
2.Pathology of Rhegmatogenous Retinal Detachment.
Journal of the Korean Ophthalmological Society 1974;15(3):221-224
Description histopathologic pictures of rhegmatogenous retinal dctachment in its early stase to late stage is reviewed. Histology on the results of experimental retinal detachment and reattachment is introduced with short comment. Formatlon of subretinal fluid in retinal detachment is a complex and dynamic processes involving alterations in retinal and choroidal structures and metabolism of vitreal components. Peripheral retinal degenerations as predispoing features of retinal detachment are listed. Some pathologic findings following retinal detachment surgeries of clinical importances are noted briefly.
Choroid
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Metabolism
;
Pathology*
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Retinal Degeneration
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Retinal Detachment*
;
Retinaldehyde*
;
Subretinal Fluid
3.Two Cases of Ocular Albinism.
Journal of the Korean Ophthalmological Society 1980;21(4):645-647
Ocular albinism is a rare condition of abnormality in the cellular metabolism of the product of melanin in the ocular tissue. This disease is transmitted as an imtermediate sex linked recessive. This condition was first described by Nettleship in 1909. In addition, many authors described this condition. The fundamentalelinical symptoms and signs are lowered visual acuity, photophobia, nystagmus, the yellow-orange color of the fundus with the choroidal vessels perfectly visible, absence of the foveal reflex and iris that transilluminates well with scleral illumination. Recently, we experienced two cases of typical ocular albinism.
Albinism, Ocular*
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Choroid
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Iris
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Lighting
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Melanins
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Metabolism
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Photophobia
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Reflex
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Visual Acuity
4.Degradation of phagosomes and diurnal changes of lysosomes in rabbit retinal pigment epithelium.
Korean Journal of Ophthalmology 1996;10(2):82-91
Diurnal changes of lysosomes including ultrastructural changes of phagosomes and acid phosphatase reactions in phagosomes, as well as diurnal biochemical changes in cathepsin D activity, were studied in the retinal pigment epithelium (RPE) of the rabbit. The rabbit was maintained on a natural light-dark cycle over seven days in fall and was sacrificed at various times during the day and night. The number of lysosomes or phagosomes in the RPE was the highest at 1.5 hours after exposure to sunlight (8:00 AM), and thereafter decreased with time. Three types of phagosomes were observed and acid phosphatase reactions were different in each type of phagosome; the fresh phagosomes were negative or positive, lamellar bodies positive, and dense bodies partially positive. The biochemical activity of cathepsin D was the highest at 8:00 AM, and this was consistent with the time of peak in phagocytic activity in the RPE. This report shows that phagocytic activity in the RPE occurred in the early stage after exposure to sunlight, and that fresh phagosomes were sequentially degraded to lamellar or dense bodies. Cathepsin D activity also increased, and this was consistent with the phagocytic activity in the RPE.
Acid Phosphatase/metabolism
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Animals
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Cathepsin D/metabolism
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Cell Count
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Choroid/metabolism/ultrastructure
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Circadian Rhythm/*physiology
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Lysosomes/*metabolism/ultrastructure
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Phagosomes/*metabolism/ultrastructure
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Pigment Epithelium of Eye/*metabolism/ultrastructure
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Rabbits
5.Crystalline Retinopathy without Corneal Dystrophy.
Journal of the Korean Ophthalmological Society 2000;41(6):1445-1450
Bietti's crystalline retinopathy is a rare form of tapetoretinal degeneration characterized by yellow, polygonal, glistening intraretinal crystals in the posterior pole and in the superficial paralimbal cornea, which may be due to a systemic abnormality of lipid metabolism, and has been to have a autosomal recessive pattern.Also lots of the reports described similar cases without any corneal changes. 56 years-old female with complaint of progressive visual decrease had corrected visual acuity of 0.1 in her right eye and 1.0 in her left eye.Yellow intraretinal crystals with retinal pigment epithelial (RPE)dystrophy and choroidal sclerosis were noticed without any corneal changes.During follow-up for thirty months, visual acuity gradually decreased to counting fingers in her right eye and 0.7 in her left eye, and RPE degeneration and choroidal sclerosis worsened with no change in intraretinal crystals.
Choroid
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Cornea
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Crystallins*
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Female
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Fingers
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Follow-Up Studies
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Humans
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Lipid Metabolism
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Middle Aged
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Retinaldehyde
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Retinitis Pigmentosa
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Sclerosis
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Visual Acuity
6.Outflow of aqueous humor following cyclodialysis or ciliochoroidal detachment in rabbit.
Shin Hwan JOO ; Myung Kyoo KO ; Joon Kiu CHOE
Korean Journal of Ophthalmology 1989;3(2):65-69
Cyclodialysis and ciliochoroidal detachment were performed in three eyes of three rabbits and in three eyes of another three rabbits, respectively. After aspiration of the aqueous humor, 0.1 ml of 10% sodium fluorescein was injected intracamerally, and the eyeball was enucleated between 30 minutes and one hour after injection and prepared for fluorescence microscopy. Sodium fluorescein concentrations in the supraciliary space were much greater in the group with cyclodialysis or ciliochoroidal detachment than in the normal control group. These results suggest that (1) in the eye with cyclodialysis, the aqueous humor may freely gain access to the supraciliary space through the cleft between the anterior chamber and the supraciliary space and then be removed rapidly and (2) in the eye with ciliochoroidal detachment, the aqueous humor may pass through the uveoscleral outflow pathway.
Animals
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Anterior Chamber/metabolism
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Aqueous Humor/*secretion
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Choroid/metabolism/*surgery
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Ciliary Body/metabolism/*surgery
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Fluorescein
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Fluoresceins/diagnostic use
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Microscopy, Fluorescence
;
Rabbits
7.Dynamic expression of VIPR2 in form deprivation myopia.
Shuang-zhen LIU ; Hua WANG ; Jing-jing JIANG ; Ping-bao WANG ; Xiao-ying WU ; Xing-ping TAN ; Zhao-hua XIA
Journal of Central South University(Medical Sciences) 2005;30(4):456-459
OBJECTIVE:
To investigate the dynamic expression and significance of vasoactive intestinal peptide receptor 2 (VIPR2) on retina-choroid-clera in high myopia.
METHODS:
Twenty-one yellow chicks of 1 day old were used in the research. The right eyes were the experimental group, covered continuously for 1 week, 2 weeks and 4 weeks respectively. The left eyes were not covered as the normal control group. Both groups were detected diopter degrees using retinoscopic refraction, determinated eyeball axis using ophthalmology ultra-A, and investigated VIPR2 expression on retina-choroid-sclera in both groups at three stages by SP immunohistochemical staining.
RESULTS:
The experimental eyes changed from hypermetropia at pre-experiment to high myopia during the experiment stages, and the diopter degrees were deeper and eyeball axis was longer along with the period of being covered. Both groups had strong expression of VIPR2 on photoreceptor-outer segment of the retina and choroids. The expression was down-regulated with the time in both groups. Compared with the control group, VIPR2 expression of the experimental group was significantly up-regulated (P < 0.05).
CONCLUSION
Form deprivation could induce high myopia. The expression of VIPR2 existed on photoreceptor-outer segment of the retina and choroids. VIPR2 may play an important role on the formation and development of myopia.
Animals
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Animals, Newborn
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Chickens
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Choroid
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metabolism
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Female
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Male
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Myopia
;
etiology
;
metabolism
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Receptors, Vasoactive Intestinal Peptide, Type II
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biosynthesis
;
genetics
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Retina
;
metabolism
8.Atypical presentations of choroidal melanocytoma.
Xiao ZHANG ; Rong-ping DAI ; Wei-jing CHAO ; Fang-tian DONG
Chinese Medical Journal 2009;122(10):1238-1240
9.The role of Nrf2 in the alteration of tight junction protein expression in choroid plexus epithelial cells created by lanthanum-activated MMP9.
Jing SUN ; Xing Bo XU ; Hong Yue SU ; Li Cheng YAN ; Yan Shu ZHANG ; Li Jin ZHANG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2023;41(1):2-7
Objective: To investigate the effect of nuclear factor erythroid 2-related factor 2 (Nrf2) in the alteration of tight junction protein expression in choroid plexus epithelial cells created by lanthanum-activated matrix metalloproteinase 9 (MMP9) . Methods: In October 2020, immortalized rat choroid plexus epithelial cell line (Z310) cells were used as the blood-cerebrospinal fluid barrier in vitro, and were divided into control group and 0.125, 0.25, 0.5 mmol/L lanthanum chloride (LaCl(3)) treatment group. After treating Z310 cells with different concentrations of LaCl(3) for 24 hours, the morphological changes of Z310 cells were observed under inverted microscope, the protein expression levels of MMP9, occludin and zonula occludens-1 (ZO-1) were observed by cellular immunofluorescence method, and the protein expression levels of MMP9, tissue inhibitors of metalloproteinase1 (TIMP1) , occludin, ZO-1 and Nrf2 were detected by Western blotting. The level of reactive oxygen species (ROS) in cells was detected by flow cytometry. Results: Compared with the control group, Z310 cells in the LaCl(3) treatment group were smaller in size, with fewer intercellular junctions, and more dead cells and cell fragments. The expression level of MMP9 protein in cells treated with 0.25 and 0.5 mmol/L LaCl(3) was significantly higher than that in the control group (P<0.05) , and the expression level of TIMP1 and tight junction proteins occudin and ZO-1 was significantly lower than that in the control group (P<0.05) . Compared with the control group, the ROS production level in the 0.25, 0.5 mmol/L LaCl(3) treatment group was significantly increased (P<0.05) , and the Nrf2 protein expression level in the 0.125, 0.25, 0.5 mmol/L LaCl(3) treatment group was significantly decreased (P<0.05) . Conclusion: Lanthanum may increase the level of ROS in cells by down regulating the expression of Nrf2, thus activating MMP9 to reduce the expression level of intercellular tight junction proteins occludin and ZO-1.
Rats
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Animals
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Matrix Metalloproteinase 9/metabolism*
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NF-E2-Related Factor 2/metabolism*
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Tight Junction Proteins/metabolism*
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Occludin/pharmacology*
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Choroid Plexus/metabolism*
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Reactive Oxygen Species/metabolism*
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Lanthanum/pharmacology*
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Epithelial Cells
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Zonula Occludens-1 Protein/metabolism*
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Phosphoproteins/pharmacology*
10.Expression of hepcidin at the choroid plexus in normal aging rats is associated with IL-6/Stat3 signaling pathway.
Chong-Bin LIU ; Rui WANG ; Miao-Wu DONG ; Xi-Ren GAO ; Feng YU
Acta Physiologica Sinica 2014;66(6):639-646
Accumulating evidence has revealed that brain iron concentrations increase with aging, and the choroid plexus (CP) may be at the basis of iron-mediated toxicity and the increase in inflammation and oxidative stress that occurs with aging. The mechanism involves not only hepcidin, the key hormone in iron metabolism, but also iron-related proteins and signaling-transduction molecules, such as IL-6 and signal transducer and activator of transcription 3 (Stat3). The aim of the present study was to investigate the correlation between the IL-6/Stat3 signaling pathway and hepcidin at the CP in normal aging. Quantitative real time PCR and Western blot were used to determine the alterations in specific mRNA and corresponding protein changes at the CP at ages of 3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33 and 36 months in Brown-Norway/Fischer (B-N/F) rats. The results demonstrated that hepcidin mRNA level at the CP kept stable in young rats (from 3 to 18 months), and increased with aging (from 21 to 36 months). The alterations of IL-6/p-Stat3 mRNA and protein expressions in normal aging were in accordance with that of hepcidin mRNA. Our data suggest that IL-6 may regulate hepcidin expression at the CP, upon interaction with the cognate cellular receptor, and through the Stat3 signaling transduction pathway.
Aging
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physiology
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Animals
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Choroid Plexus
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metabolism
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Hepcidins
;
physiology
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Interleukin-6
;
physiology
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Iron
;
metabolism
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RNA, Messenger
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Rats
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Rats, Inbred F344
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STAT3 Transcription Factor
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physiology
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Signal Transduction