Nussenzveig D R, Lewicki J A, Maack T
Department of Physiology, Cornell University Medical College, New York, New York 10021.
J Biol Chem. 1990 Dec 5;265(34):20952-8.
Clearance (C) receptors of atrial natriuretic factor (ANF) have an important role of removing ANF from the circulation. In the present study we investigated the cellular mechanisms of this function. 125I-ANF1-28 specifically bound to C-ANF receptors in cultured bovine vascular smooth muscle cells is internalized by a temperature-dependent process at a rate of 5% occupied receptors/min at 37 degrees C. Internalized 125I-ANF1-28 is rapidly metabolized and released to the medium as [125I]monoiodotyrosine, a process that is reversibly inhibited by NH4Cl (10 mM). Retroendocytosis of receptor-ligand complex is detectable when intracellular accumulation of the ligand is maximized by previous incubation with NH4Cl. In the presence of saturating concentrations of 125I-ANF1-28 when cells are warmed from 4 to 37 degrees C, there is first a decrease and then an almost complete replenishment of surface C-ANF receptors, a phenomenon that is not altered by protein synthesis inhibition with cycloheximide. In the absence of temperature transition, the density of surface C-ANF receptors remains constant, and by 2 h of incubation the amount of ANF hydrolyzed far exceeds the total amount of C-ANF receptors. The total population of surface C-ANF receptors is internalized and recycled every hour, and these processes are constitutive since they also occur in the absence of ligand. Trypsinization and solubilization experiments further indicate that C-ANF receptors are rapidly internalized and recycled to the cell membrane. The results demonstrate that receptor-ligand internalization, extensive receptor recycling, and lysosomal hydrolysis of ANF are the cellular mechanisms by which C-ANF receptors exert their clearance function.
心房利钠因子(ANF)的清除(C)受体在从循环中清除ANF方面具有重要作用。在本研究中,我们研究了该功能的细胞机制。125I-ANF1-28特异性结合培养的牛血管平滑肌细胞中的C-ANF受体,并通过温度依赖性过程内化,在37℃时以5%的占据受体/分钟的速率进行。内化的125I-ANF1-28迅速代谢并以[125I]单碘酪氨酸的形式释放到培养基中,这一过程被NH4Cl(10 mM)可逆性抑制。当通过先前用NH4Cl孵育使配体在细胞内的积累最大化时,可检测到受体-配体复合物的逆向内吞作用。在存在饱和浓度的125I-ANF1-28的情况下,当细胞从4℃升温至37℃时,首先表面C-ANF受体减少,然后几乎完全补充,这种现象不会因用环己酰亚胺抑制蛋白质合成而改变。在没有温度转变的情况下,表面C-ANF受体的密度保持恒定,并且孵育2小时后水解的ANF量远远超过C-ANF受体的总量。表面C-ANF受体的总数每小时内化并循环一次,并且这些过程是组成性的,因为它们在没有配体的情况下也会发生。胰蛋白酶消化和溶解实验进一步表明,C-ANF受体迅速内化并循环回到细胞膜。结果表明,受体-配体内化、广泛的受体循环以及ANF的溶酶体水解是C-ANF受体发挥其清除功能的细胞机制。