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Endocytosis of glycosylphosphatidylinositol-anchored proteins
Glycosylphosphatidylinositol-anchored proteins (GPI-APs) represent an interesting amalgamation of the three basic kinds of cellular macromolecules viz. proteins, carbohydrates and lipids. An unusually hybrid moiety, the GPI-anchor is expressed in a diverse range of organisms from parasites to mammal...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2764642/ https://www.ncbi.nlm.nih.gov/pubmed/19832981 http://dx.doi.org/10.1186/1423-0127-16-93 |
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author | Lakhan, Shaheen E Sabharanjak, Shefali De, Ananya |
author_facet | Lakhan, Shaheen E Sabharanjak, Shefali De, Ananya |
author_sort | Lakhan, Shaheen E |
collection | PubMed |
description | Glycosylphosphatidylinositol-anchored proteins (GPI-APs) represent an interesting amalgamation of the three basic kinds of cellular macromolecules viz. proteins, carbohydrates and lipids. An unusually hybrid moiety, the GPI-anchor is expressed in a diverse range of organisms from parasites to mammalian cells and serves to anchor a large number of functionally diverse proteins and has been the center of attention in scientific debate for some time now. Membrane organization of GPI-APs into laterally-organized cholesterol-sphingolipid ordered membrane domains or "rafts" and endocytosis of GPI-APs has been intensely debated. Inclusion into or exclusion from these membrane domains seems to be the critical factor in determining the endocytic mechanisms and intracellular destinations of GPI-APs. The intracellular signaling as well as endocytic trafficking of GPI-APs is critically dependent upon the cell surface organization of GPI-APs, and the associations with these lipid rafts play a vital role during these processes. The mechanism of endocytosis for GPI-APs may differ from other cellular endocytic pathways, such as those mediated by clathrin-coated pits (caveolae), and is necessary for unique biological functions. Numerous intracellular factors are involved in and regulate the endocytosis of GPI-APs, and these may be variably dependent on cell-type. The central focus of this article is to describe the significance of the endocytosis of GPI-APs on a multitude of biological processes, ranging from nutrient-uptake to more complex immune responses. Ultimately, a thorough elucidation of GPI-AP mediated signaling pathways and their regulatory elements will enhance our understanding of essential biological processes and benefit as components of disease intervention strategies. |
format | Text |
id | pubmed-2764642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27646422009-10-21 Endocytosis of glycosylphosphatidylinositol-anchored proteins Lakhan, Shaheen E Sabharanjak, Shefali De, Ananya J Biomed Sci Review Glycosylphosphatidylinositol-anchored proteins (GPI-APs) represent an interesting amalgamation of the three basic kinds of cellular macromolecules viz. proteins, carbohydrates and lipids. An unusually hybrid moiety, the GPI-anchor is expressed in a diverse range of organisms from parasites to mammalian cells and serves to anchor a large number of functionally diverse proteins and has been the center of attention in scientific debate for some time now. Membrane organization of GPI-APs into laterally-organized cholesterol-sphingolipid ordered membrane domains or "rafts" and endocytosis of GPI-APs has been intensely debated. Inclusion into or exclusion from these membrane domains seems to be the critical factor in determining the endocytic mechanisms and intracellular destinations of GPI-APs. The intracellular signaling as well as endocytic trafficking of GPI-APs is critically dependent upon the cell surface organization of GPI-APs, and the associations with these lipid rafts play a vital role during these processes. The mechanism of endocytosis for GPI-APs may differ from other cellular endocytic pathways, such as those mediated by clathrin-coated pits (caveolae), and is necessary for unique biological functions. Numerous intracellular factors are involved in and regulate the endocytosis of GPI-APs, and these may be variably dependent on cell-type. The central focus of this article is to describe the significance of the endocytosis of GPI-APs on a multitude of biological processes, ranging from nutrient-uptake to more complex immune responses. Ultimately, a thorough elucidation of GPI-AP mediated signaling pathways and their regulatory elements will enhance our understanding of essential biological processes and benefit as components of disease intervention strategies. BioMed Central 2009-10-15 /pmc/articles/PMC2764642/ /pubmed/19832981 http://dx.doi.org/10.1186/1423-0127-16-93 Text en Copyright ©2009 Lakhan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Lakhan, Shaheen E Sabharanjak, Shefali De, Ananya Endocytosis of glycosylphosphatidylinositol-anchored proteins |
title | Endocytosis of glycosylphosphatidylinositol-anchored proteins |
title_full | Endocytosis of glycosylphosphatidylinositol-anchored proteins |
title_fullStr | Endocytosis of glycosylphosphatidylinositol-anchored proteins |
title_full_unstemmed | Endocytosis of glycosylphosphatidylinositol-anchored proteins |
title_short | Endocytosis of glycosylphosphatidylinositol-anchored proteins |
title_sort | endocytosis of glycosylphosphatidylinositol-anchored proteins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2764642/ https://www.ncbi.nlm.nih.gov/pubmed/19832981 http://dx.doi.org/10.1186/1423-0127-16-93 |
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