Craven P A, DeRubertis F R
Biochemistry. 1976 Nov 16;15(23):5131-7. doi: 10.1021/bi00668a029.
The properties of the guanylate cyclase systems of outer and inner medulla of rat kidney were examined and compared with those of the renal cortex. A gradation in steady-state cyclic guanosine 3',5'-monophosphate (cGMP) levels was observed in incubated slices of these tissues (inner medula greater than outer medulla greater than cortex). This correlated with the proportion of total guanyl cyclase activity in the 100 000 g particulate fraction of each tissue, but was discordant with the relative activities of guanylate cyclase (highest in cortex) and of cGMP-phosphodiesterase (lowest in cortex) in whole tissue homogenates. Soluble guanylate cyclase of cortex and inner medulla exhibited typical Michaelis-Menten kinetics with an apparent Km for MnGTP of 0.11 mM, while the particulate enzyme from inner medulla exhibited apparent positive cooperative behavior and a decreased dependence on Mn2+. Thus, the particulate enzyme could play a key role in regulating cGMP levels inthe intact cell where Mn2+ concentrations are low. The soluble and particulate enzymes from inner medulla were further distinguished by their responses to several test agents. The soluble enzyme was activated by Ca2+, NaN3, NaNo2 and phenylhydrazine, whereas particulate activity was inhibited by Ca2+ and was unresponsive to the latter agents. In the presence of NaNo2, Mn2+ requirement of the soluble enzyme was reduced and equivalent to that of the particulate preparation. Moreover, relative responsiveness of the sollble enzyme to NaNO2 was potentiated when Mg2+ replaced Mn2+ as the sole divalent cation. These changes in metal requirements may be involved in the action of NaNO2 to increase cGMP in intact kidney. Soluble guanylate cyclase of cortex was clearly more responsive to stimulation by NaN3, Nano2, and phenylhydrazine that was soluble activity from either medullary tissue. The effectiveness of the agonists on soluble activity from outer and inner medulla cound also be distinguished. Accordingly, regulation and properties of soluble guanylate cyclase, as well as subcellular enzyme distribution, and distinct in the three regions of the kidney.
对大鼠肾脏外髓质和内髓质的鸟苷酸环化酶系统的特性进行了检测,并与肾皮质的特性进行了比较。在这些组织的孵育切片中观察到稳态环鸟苷酸(cGMP)水平存在梯度变化(内髓质>外髓质>皮质)。这与每个组织100000g颗粒部分中总鸟苷酸环化酶活性的比例相关,但与全组织匀浆中鸟苷酸环化酶(皮质中最高)和cGMP磷酸二酯酶(皮质中最低)的相对活性不一致。皮质和内髓质的可溶性鸟苷酸环化酶表现出典型的米氏动力学,对MnGTP的表观Km为0.11 mM,而来自内髓质的颗粒酶表现出明显的正协同行为,对Mn2+的依赖性降低。因此,颗粒酶可能在完整细胞中Mn2+浓度较低时调节cGMP水平方面起关键作用。来自内髓质的可溶性和颗粒酶通过它们对几种测试剂的反应进一步区分。可溶性酶被Ca2+、NaN3、NaNO2和苯肼激活,而颗粒活性被Ca2+抑制,对后几种试剂无反应。在存在NaNO2的情况下,可溶性酶对Mn2+的需求降低,与颗粒制剂相当。此外,当Mg2+取代Mn2+作为唯一的二价阳离子时,可溶性酶对NaNO2的相对反应性增强。金属需求的这些变化可能参与了NaNO2在完整肾脏中增加cGMP的作用。皮质的可溶性鸟苷酸环化酶对NaN3、NaNO2和苯肼刺激的反应明显比对任何一种髓质组织的可溶性活性更敏感。激动剂对来自外髓质和内髓质的可溶性活性的有效性也可以区分。因此,可溶性鸟苷酸环化酶的调节和特性,以及亚细胞酶分布,在肾脏的三个区域是不同的。