کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6196928 1602596 2014 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Plasma membrane protein polarity and trafficking in RPE cells: Past, present and future
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی و میکروب شناسی (عمومی)
پیش نمایش صفحه اول مقاله
Plasma membrane protein polarity and trafficking in RPE cells: Past, present and future
چکیده انگلیسی


- The retinal support functions of RPE require polarized plasma membrane (PM) proteins.
- PM protein polarity in RPE is different from that of conventional epithelia.
- The sorting signals, machinery and trafficking routes of PM proteins in RPE are only partly known.
- RPE trafficking mechanisms were studied in RPE cell lines or extrapolated from MDCK cells.
- Novel microscopy techniques will expand our understanding of RPE polarity and trafficking.

The retinal pigment epithelium (RPE) comprises a monolayer of polarized pigmented epithelial cells that is strategically interposed between the neural retina and the fenestrated choroid capillaries. The RPE performs a variety of vectorial transport functions (water, ions, metabolites, nutrients and waste products) that regulate the composition of the subretinal space and support the functions of photoreceptors (PRs) and other cells in the neural retina. To this end, RPE cells display a polarized distribution of channels, transporters and receptors in their plasma membrane (PM) that is remarkably different from that found in conventional extra-ocular epithelia, e.g. intestine, kidney, and gall bladder. This characteristic PM protein polarity of RPE cells depends on the interplay of sorting signals in the RPE PM proteins and sorting mechanisms and biosynthetic/recycling trafficking routes in the RPE cell. Although considerable progress has been made in our understanding of the RPE trafficking machinery, most available data have been obtained from immortalized RPE cell lines that only partially maintain the RPE phenotype and by extrapolation of data obtained in the prototype Madin-Darby Canine Kidney (MDCK) cell line. The increasing availability of RPE cell cultures that more closely resemble the RPE in vivo together with the advent of advanced live imaging microscopy techniques provides a platform and an opportunity to rapidly expand our understanding of how polarized protein trafficking contributes to RPE PM polarity.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Experimental Eye Research - Volume 126, September 2014, Pages 5-15
نویسندگان
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