VISUALIZATION OF THE THYROTROPIN-RELEASING-HORMONE RECEPTOR AND ITS LIGAND DURING ENDOCYTOSIS AND RECYCLING
VISUALIZATION OF THE THYROTROPIN-RELEASING-HORMONE RECEPTOR AND ITS LIGAND DURING ENDOCYTOSIS AND RECYCLING
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DOI:
10.1073/pnas.92.2.512
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发表时间:
1995-01-17
影响因子:
11.1
通讯作者:
HINKLE, PM
中科院分区:
文献类型:
--
作者:
ASHWORTH, R;YU, R;HINKLE, PM
Endocytosis and recycling of both thyrotropin-releasing hormone (TRH) and its G-protein coupled receptor were visualized by conventional and confocal fluorescence microscopy in pituitary cells using a rhodamine-labeled TRH analog (Rhod-TRH) and indirect immunofluorescent staining of cells stably transfected with an epitope-tagged TRH receptor (TRHR), The epitope-tagged TRHR was confined to the cell surface prior to agonist treatment. Both Rhod-TRH and TRHR were also localized on the plasma membrane after agonist binding at 0 degrees C, Ligand binding at 37 degrees C resulted in rapid endocytosis, and both Rhod-TRH and the epitope-tagged TRHR appeared in cytoplasmic vesicles within 5 min, Fluorescently labeled TRH and transferrin colocalized in the same endocytotic vesicles, and internalization of Rhod-TRH and TRHR was inhibited by hypertonic medium, suggesting that endocytosis occurred by a clathrin-dependent mechanism, Internalized TRHRs returned to the membrane within 20 min after removal of TRH, and cycloheximide did not block receptor recycling, A mutant TRHR truncated at Cys(335) Signaled but did not internalize Rhod-TRH, confirming the importance of the carboxyl terminus of the TRHR in receptor-mediated endocytosis. Thus, the TRH-TRHR complex is endocytosed via clathrin-coated vesicles and the receptor is recycled to the plasma membrane.