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Angiotensin II (AngII) initiates a variety of cellular responses through activation of type 1 (AT(1); with subtypes AT(1a) and AT(1b) ) and type 2 (AT(2) ) cell surface angiotensin receptors. Both AT(1) and AT(2) receptors couple to heterotrimeric guanyl nucleotide binding proteins (G-proteins) and generate intracellular signals following recognition of extracellular AngII, but only AT(1) is targeted for the rapid ligand-stimulated endocytosis (internalization) typical of many plasma membrane receptors. 2. AT(1) endocytosis proceeds through clathrin-coated pits and is independent of G-protein coupling which predicts that the AngII-AT(1) receptor complex attains a conformation necessary for interaction with the endocytotic machinery, but separate from receptor signalling activation. 3. The function of AT(1) endocytosis and the reason for the disparity between AT(1) and AT(2) endocytosis is not fully appreciated, but the latter probably reflects differences in the primary amino acid sequence of these two receptor types. 4. For many receptors that undergo internalization, it has been established that internalization motifs (2-6 amino acids, often incorporating crucial tyrosine and hydrophobic amino acids) within the cytoplasmic regions of the receptor mediate the selective recruitment of activated receptors into clathrin-coated pits and vesicles. 5. Mutagenesis studies on the AT(1a) receptor, aimed at identifying such motifs, reveal that sites within the third cytoplasmic loop and the cytoplasmic carboxyl terminal region are important for AngII-stimulated AT(1a) receptor endocytosis.
Thomas et al. (Sun,) studied this question.