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The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway

The folate receptor, also known as the membrane folate-binding protein, is maximally expressed on the surface of folate-depleted tissue culture cells and mediates the high affinity accumulation of 5- methyltetrahydrofolic acid in the cytoplasm of these cells. Recent evidence suggests that this recep...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2116044/
https://www.ncbi.nlm.nih.gov/pubmed/1968465
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collection PubMed
description The folate receptor, also known as the membrane folate-binding protein, is maximally expressed on the surface of folate-depleted tissue culture cells and mediates the high affinity accumulation of 5- methyltetrahydrofolic acid in the cytoplasm of these cells. Recent evidence suggests that this receptor recycles during folate internalization and that it is anchored in the membrane by a glycosyl- phosphatidylinositol linkage. Using quantitative immunocytochemistry, we now show that (a) this receptor is highly clustered on the cell surface; (b) these clusters are preferentially associated with uncoated membrane invaginations rather than clathrin-coated pits; and (c) the receptor is not present in endosomes or lysosomes. This receptor appears to physically move in and out of the cell using a novel uncoated pit pathway that does not merge with the clathrin-coated pit endocytic machinery.
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spelling pubmed-21160442008-05-01 The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway J Cell Biol Articles The folate receptor, also known as the membrane folate-binding protein, is maximally expressed on the surface of folate-depleted tissue culture cells and mediates the high affinity accumulation of 5- methyltetrahydrofolic acid in the cytoplasm of these cells. Recent evidence suggests that this receptor recycles during folate internalization and that it is anchored in the membrane by a glycosyl- phosphatidylinositol linkage. Using quantitative immunocytochemistry, we now show that (a) this receptor is highly clustered on the cell surface; (b) these clusters are preferentially associated with uncoated membrane invaginations rather than clathrin-coated pits; and (c) the receptor is not present in endosomes or lysosomes. This receptor appears to physically move in and out of the cell using a novel uncoated pit pathway that does not merge with the clathrin-coated pit endocytic machinery. The Rockefeller University Press 1990-03-01 /pmc/articles/PMC2116044/ /pubmed/1968465 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway
title The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway
title_full The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway
title_fullStr The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway
title_full_unstemmed The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway
title_short The glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway
title_sort glycophospholipid-linked folate receptor internalizes folate without entering the clathrin-coated pit endocytic pathway
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2116044/
https://www.ncbi.nlm.nih.gov/pubmed/1968465