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PMID: 6310570 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Isolation and characterization of a highly enriched preparation of receptosomes (endosomes) from a human cell line.

Dickson RB, Beguinot L, Hanover JA, Richert ND, Willingham MC, Pastan I

Abstract

Receptor-mediated endocytosis proceeds by transfer of receptor-ligand complexes from clathrin-coated pits at the cell surface to uncoated endocytic vesicles termed receptosomes (or endosomes). These vesicles have now been purified more than 37-fold based on their content of newly internalized epidermal growth factor. 125I-labeled EGF was bound to human KB carcinoma cells at 4 degrees C, and then the cells were warmed to 37 degrees C for 8 min and disrupted. The purification scheme involved density gradient centrifugation on colloidal silica and sucrose and gel filtration on Sephacryl S-1000. Relative to homogenate, receptosomes are enriched 4.3-fold in their cholesterol content and depleted in enzyme markers for plasma membranes (2- to 3-fold) and lysosomes (9-fold). Receptosomes have a polypeptide composition that is different from plasma membrane, lysosome, and other homogenate fractions. They are enriched in transferrin receptors (30-fold) and in unidentified Mr 70,000-75,000 glycoprotein(s); they contain phosphomannosyl receptors. They do not contain detectable amounts of clathrin.

MeSH Terms
Carcinoma Cell Line Cell Membrane/physiology,ultrastructure Endocytosis Humans Lysosomes/ultrastructure Microscopy, Electron Mouth Neoplasms Receptors, Cell Surface/isolation & purification,physiology
Chemicals
Receptors, Cell Surface
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Dickson R B
Beguinot L
Hanover J A
Richert N D
Willingham M C
Pastan I
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30 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1983-09-00
Pages
5335-9
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC384250
Subset
IM
Grants
NIADDK NIH HHS · F32 AM06318-OS · United States
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