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Chloroquine allows the secretion of internalized SVI-epidermal growth factor from fibroblasts

Journal Article · · J. Cell. Physiol.; (United States)
Incubation of cells with labelled hormone in the presence of the lysosomotropic agent chloroquine produces an enhanced intracellular accumulation of hormone and receptor. Using a pulse-chase paradigm in which cell surface receptors were labelled with SVI-EGF at 4 degrees C, it was found that when 100 microM chloroquine was present in the 37 degrees C chase medium intact hormone was accumulated in the medium. Without chloroquine, low molecular weight (mw) degradation products were found in the medium. The processes of receptor-mediated endocytosis and subcellular distribution of SVI-EGF-receptor complexes were unchanged by chloroquine. The source of the intact hormone accumulating in the medium was therefore an intracellular compartment(s). The SVI-EGF released from the cells could rebind to surface receptors and be re-internalized; rebinding was inhibited by unlabelled EGF or Concanavalin A in the incubation medium. The concentration of unlabelled EGF required to inhibit rebinding was more than three orders of magnitude greater than the amount of SVI-EGF whose rebinding was inhibited. Thus, the SVI-EGF released from intracellular sites was rebound preferentially over exogenous EGF. The possible pathways for secretion of intact SVI-EGF and mechanisms of its preferential rebinding are discussed.
Research Organization:
Los Alamos National Lab., NM
OSTI ID:
6331732
Journal Information:
J. Cell. Physiol.; (United States), Journal Name: J. Cell. Physiol.; (United States) Vol. 2; ISSN JCLLA
Country of Publication:
United States
Language:
English

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