Matches in SemOpenAlex for { <https://semopenalex.org/work/W2069421982> ?p ?o ?g. }
- W2069421982 endingPage "2121" @default.
- W2069421982 startingPage "2116" @default.
- W2069421982 abstract "Cell-surface receptors that undergo clathrin-mediated endocytosis contain short amino acid sequences in their cytoplasmic domain that serve as internalization signals. Interactions between these sequences and components of the endocytic machinery should become limiting upon overexpression of the constitutively recycling transferrin receptor (TfR). A tetracycline-responsive system was used to induce overexpression of the TfR up to 20-fold in HeLa cells. Internalization assays indicate the rate of 125I-transferrin uptake per surface TfR is reduced by a factor of 4 in induced cells. Consistent with endocytosis being the rate-limiting step, TfRs shift from an endosomal to more of a plasma membrane distribution with TfR overexpression. The clathrin-associated protein AP-2 has been proposed to interact directly with the cytoplasmic domain of many receptors, yet no changes in the amount or distribution of AP-2 were detected in induced cells. The internalization rate for the epidermal growth factor receptor was also measured, with or without induction of TfR expression. Even though endocytosis of the TfR is saturated in induced cells, 125I-labeled epidermal growth factor continues to be internalized at a rate identical to that seen in uninduced cells. We propose that there are different limiting steps for the endocytosis of these two receptors. Cell-surface receptors that undergo clathrin-mediated endocytosis contain short amino acid sequences in their cytoplasmic domain that serve as internalization signals. Interactions between these sequences and components of the endocytic machinery should become limiting upon overexpression of the constitutively recycling transferrin receptor (TfR). A tetracycline-responsive system was used to induce overexpression of the TfR up to 20-fold in HeLa cells. Internalization assays indicate the rate of 125I-transferrin uptake per surface TfR is reduced by a factor of 4 in induced cells. Consistent with endocytosis being the rate-limiting step, TfRs shift from an endosomal to more of a plasma membrane distribution with TfR overexpression. The clathrin-associated protein AP-2 has been proposed to interact directly with the cytoplasmic domain of many receptors, yet no changes in the amount or distribution of AP-2 were detected in induced cells. The internalization rate for the epidermal growth factor receptor was also measured, with or without induction of TfR expression. Even though endocytosis of the TfR is saturated in induced cells, 125I-labeled epidermal growth factor continues to be internalized at a rate identical to that seen in uninduced cells. We propose that there are different limiting steps for the endocytosis of these two receptors." @default.
- W2069421982 created "2016-06-24" @default.
- W2069421982 creator A5033221123 @default.
- W2069421982 creator A5044002256 @default.
- W2069421982 creator A5059139062 @default.
- W2069421982 date "1997-01-01" @default.
- W2069421982 modified "2023-09-26" @default.
- W2069421982 title "Saturation of the Endocytic Pathway for the Transferrin Receptor Does Not Affect the Endocytosis of the Epidermal Growth Factor Receptor" @default.
- W2069421982 cites W1211619533 @default.
- W2069421982 cites W1487627529 @default.
- W2069421982 cites W149688775 @default.
- W2069421982 cites W1504143645 @default.
- W2069421982 cites W1515946344 @default.
- W2069421982 cites W1519083075 @default.
- W2069421982 cites W1521301888 @default.
- W2069421982 cites W1523766194 @default.
- W2069421982 cites W1526795140 @default.
- W2069421982 cites W1535731511 @default.
- W2069421982 cites W1565751394 @default.
- W2069421982 cites W1583703772 @default.
- W2069421982 cites W1607784649 @default.
- W2069421982 cites W1807013767 @default.
- W2069421982 cites W1807118481 @default.
- W2069421982 cites W1967436918 @default.
- W2069421982 cites W1968164116 @default.
- W2069421982 cites W1969882621 @default.
- W2069421982 cites W1974639063 @default.
- W2069421982 cites W1979757599 @default.
- W2069421982 cites W1979815209 @default.
- W2069421982 cites W2027615173 @default.
- W2069421982 cites W2029991413 @default.
- W2069421982 cites W2030634945 @default.
- W2069421982 cites W2033175618 @default.
- W2069421982 cites W2034556361 @default.
- W2069421982 cites W2035584408 @default.
- W2069421982 cites W2042238592 @default.
- W2069421982 cites W2044343226 @default.
- W2069421982 cites W2049645388 @default.
- W2069421982 cites W2050960932 @default.
- W2069421982 cites W2054537734 @default.
- W2069421982 cites W2059031237 @default.
- W2069421982 cites W2061462231 @default.
- W2069421982 cites W2067691363 @default.
- W2069421982 cites W2071846646 @default.
- W2069421982 cites W2080066315 @default.
- W2069421982 cites W2090429649 @default.
- W2069421982 cites W2095606352 @default.
- W2069421982 cites W2100047958 @default.
- W2069421982 cites W2114361525 @default.
- W2069421982 cites W2128840474 @default.
- W2069421982 cites W2133809169 @default.
- W2069421982 cites W2165610167 @default.
- W2069421982 cites W2178812731 @default.
- W2069421982 cites W311244383 @default.
- W2069421982 cites W348795408 @default.
- W2069421982 cites W6167358 @default.
- W2069421982 doi "https://doi.org/10.1074/jbc.272.4.2116" @default.
- W2069421982 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/8999911" @default.
- W2069421982 hasPublicationYear "1997" @default.
- W2069421982 type Work @default.
- W2069421982 sameAs 2069421982 @default.
- W2069421982 citedByCount "109" @default.
- W2069421982 countsByYear W20694219822012 @default.
- W2069421982 countsByYear W20694219822013 @default.
- W2069421982 countsByYear W20694219822014 @default.
- W2069421982 countsByYear W20694219822015 @default.
- W2069421982 countsByYear W20694219822016 @default.
- W2069421982 countsByYear W20694219822017 @default.
- W2069421982 countsByYear W20694219822018 @default.
- W2069421982 countsByYear W20694219822019 @default.
- W2069421982 countsByYear W20694219822020 @default.
- W2069421982 countsByYear W20694219822021 @default.
- W2069421982 countsByYear W20694219822023 @default.
- W2069421982 crossrefType "journal-article" @default.
- W2069421982 hasAuthorship W2069421982A5033221123 @default.
- W2069421982 hasAuthorship W2069421982A5044002256 @default.
- W2069421982 hasAuthorship W2069421982A5059139062 @default.
- W2069421982 hasBestOaLocation W20694219821 @default.
- W2069421982 hasConcept C102747710 @default.
- W2069421982 hasConcept C117943116 @default.
- W2069421982 hasConcept C139770010 @default.
- W2069421982 hasConcept C170493617 @default.
- W2069421982 hasConcept C190062978 @default.
- W2069421982 hasConcept C22814914 @default.
- W2069421982 hasConcept C2776362946 @default.
- W2069421982 hasConcept C2779438470 @default.
- W2069421982 hasConcept C28005876 @default.
- W2069421982 hasConcept C32264632 @default.
- W2069421982 hasConcept C55493867 @default.
- W2069421982 hasConcept C63162447 @default.
- W2069421982 hasConcept C79747257 @default.
- W2069421982 hasConcept C79879829 @default.
- W2069421982 hasConcept C86803240 @default.
- W2069421982 hasConcept C95444343 @default.
- W2069421982 hasConceptScore W2069421982C102747710 @default.
- W2069421982 hasConceptScore W2069421982C117943116 @default.
- W2069421982 hasConceptScore W2069421982C139770010 @default.
- W2069421982 hasConceptScore W2069421982C170493617 @default.