نتایج جستجو برای: human retinal pigment epithelium cell

تعداد نتایج: 3004906  

Journal: :Investigative ophthalmology & visual science 1996
J Ortego J Escribano S P Becerra M Coca-Prados

PURPOSE To study the expression of the neurotrophic pigment epithelium-derived factor (PEDF), a protein with neurotrophic and neuronal-survival activities, by the human ocular ciliary epithelium. METHODS Total RNA extracted from human and bovine ocular tissues were screened by Northern blot analysis with cDNA probes for PEDF. Antibodies to PEDF were used to monitor its synthesis and secretion...

Journal: :Molecular & cellular proteomics : MCP 2003
Karen A West Lin Yan Karen Shadrach Jian Sun Azeem Hasan Masaru Miyagi John S Crabb Joe G Hollyfield Alan D Marmorstein John W Crabb

The retinal pigment epithelium (RPE) is a single cell layer adjacent to the rod and cone photoreceptors that plays key roles in retinal physiology and the biochemistry of vision. RPE cells were isolated from normal adult human donor eyes, subcellular fractions were prepared, and proteins were fractionated by electrophoresis. Following in-gel proteolysis, proteins were identified by peptide sequ...

Journal: :Investigative ophthalmology & visual science 1986
R Yamakawa N Ogino

Prostaglandin synthetic activity of neural retina and retinal pigment epithelium in chick retina was studied using arachidonic acid and prostaglandin H2 (intermediate prostaglandin endoperoxide) as substrates. To obtain sufficient enzyme activity in retinal pigment epithelium, cultured chick retinal pigment epithelial cells were used. Little arachidonic acid was converted into prostaglandins, a...

جوان, محمد, پروینی, مریم, کاظم, پریور,

Pluripotent stem cells as the cells with a capacity for self-renewal and differentiation into various specificcell types have been highly regarded in regenerative medicine studies. To repair the eye disease damages, thedifferentiation into retinal pigment epithelial cells of pluripotent stem cells has gained great importance inrecent decades because the inappropriate function of these cells is ...

2014
Ramzi M. Alameddine Ahmad M. Mansour Eman Kahtani

Choroidal osteomas are rare benign ossifying tumors that appear as irregular slightly elevated, yellow-white, juxtapapillary, choroidal mass with well-defined geographic borders, depigmentation of the overlying pigment epithelium; and with multiple small vascular networks on the tumor surface. Visual loss results from three mechanisms: Atrophy of the retinal pigment epithelium overlying a decal...

Journal: :Investigative ophthalmology & visual science 2008
Bartosz Rózanowski Janice M Burke Michael E Boulton Tadeusz Sarna Małgorzata Rózanowska

PURPOSE To determine the effects of human retinal pigment epithelial (RPE) cell pigment granules on photosensitized and iron ion-mediated oxidation and the effect of the photodegradation of melanosomes on their antioxidant properties. METHODS RPE cells were isolated from human and bovine eyes; pigmented and nonpigmented bovine retinal pigment epithelia were isolated separately. Melanosomes, m...

Journal: :Investigative ophthalmology & visual science 1993
M L Katz H J Stientjes C L Gao J S Christianson

PURPOSE One of the most prominent changes that occurs in the retinal pigment epithelium during senescence is the progressive accumulation of the autofluorescent pigment lipofuscin. Experiments were conducted to evaluate the role of nonenzymatic oxidation of photoreceptor outer segments in retinal pigment epithelium lipofuscin formation. METHODS Albino Fischer rats were given intravitreal inje...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
William A Beltran Artur V Cideciyan Alfred S Lewin Simone Iwabe Hemant Khanna Alexander Sumaroka Vince A Chiodo Diego S Fajardo Alejandro J Román Wen-Tao Deng Malgorzata Swider Tomas S Alemán Sanford L Boye Sem Genini Anand Swaroop William W Hauswirth Samuel G Jacobson Gustavo D Aguirre

Hereditary retinal blindness is caused by mutations in genes expressed in photoreceptors or retinal pigment epithelium. Gene therapy in mouse and dog models of a primary retinal pigment epithelium disease has already been translated to human clinical trials with encouraging results. Treatment for common primary photoreceptor blindness, however, has not yet moved from proof of concept to the cli...

2013
Charles W. Higdon Robi D. Mitra Stephen L. Johnson

In order to facilitate understanding of pigment cell biology, we developed a method to concomitantly purify melanocytes, iridophores, and retinal pigmented epithelium from zebrafish, and analyzed their transcriptomes. Comparing expression data from these cell types and whole embryos allowed us to reveal gene expression co-enrichment in melanocytes and retinal pigmented epithelium, as well as in...

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