Wang J M, Llona I, De Potter W P
Department of Medicine, University of Antwerp (UIA), Wilrijk, Belgium.
Regul Pept. 1994 Aug 31;53(1):77-86. doi: 10.1016/0167-0115(94)90161-9.
Binding and internalization of angiotensin II (AII) were studied on bovine adrenal medullary cells in primary culture. Binding of [125I]AII was reversible, saturable, specific and showed high affinity. AII was found to be internalized by bovine adrenal medullary cells. Monensin increased whereas phenylarsine oxide (PhAsO) decreased the internalization. Excess of unlabelled AII or saralasin could block the internalization, indicating a receptor mediated internalization process. The kinetic analysis indicated that, during the first 4 min, about 25% of the membrane bound ligand was internalized per min and the recycling of internalized ligand and receptor initiated around 4 min.
在原代培养的牛肾上腺髓质细胞上研究了血管紧张素II(AII)的结合与内化。[125I]AII的结合是可逆的、可饱和的、特异性的且具有高亲和力。发现AII可被牛肾上腺髓质细胞内化。莫能菌素增加而苯砷酸氧化物(PhAsO)减少内化。过量的未标记AII或沙拉新可阻断内化,表明这是一个受体介导的内化过程。动力学分析表明,在最初4分钟内,每分钟约25%的膜结合配体被内化,内化配体和受体的再循环在4分钟左右开始。