Lewko B, Gołos M, Latawiec E, Angielski S, Stepinski J
Department of Immunopathology, Medical University of Gdansk, Gdansk, Poland.
J Physiol Pharmacol. 2006 Dec;57(4):599-610.
The podocytes are highly differentiated cells playing a key role in glomerular filtration. Vasoactive factors including angiotensin II (Ang II) and cyclic guanosine 5' monophosphate (cGMP) are synthesized by these cells upon stimulation as well as in the basal state. In this study we have tested whether angiotensin II affects the total synthesis of cGMP in primary culture of rat podocytes. The cells were stimulated with atrial natriuretic peptide (ANP) and/or a nitric oxide (NO) donor, S-nitroso-N-acetyl penicillamine (SNAP), in the absence or presence of Ang II. The cGMP synthesis was determined by radioimmunoassay (RIA). ANP or SNAP alone increased the cGMP synthesis in podocytes although the effects were not additive unless Ang II was present in the medium. Ang II suppressed the ANP-dependent cGMP synthesis whereas SNAP-dependent cGMP production remained unaffected. These effects were prevented by a non-specific antagonist of Ang II receptors (AT), saralasin. Adversely, PD123319, a specific inhibitor of AT2 receptors, augmented inhibition of ANP-dependent and enhanced the NO-dependent cGMP production. Probenecid, an inhibitor of cGMP extrusion from the cells, suppressed the cGMP generation by both ANP and SNAP. We conclude that cGMP synthesis in cultured podocytes is modulated by angiotensin II and that two adversely acting receptors, AT1 and AT2 are involved in this effect. Additionally, production of cGMP might be intrinsically inhibited by cGMP accumulating inside the cells.
足细胞是高度分化的细胞,在肾小球滤过中起关键作用。血管活性因子,包括血管紧张素II(Ang II)和环磷酸鸟苷(cGMP),在这些细胞受到刺激时以及基础状态下都会合成。在本研究中,我们测试了血管紧张素II是否会影响大鼠足细胞原代培养物中cGMP的总合成。在不存在或存在Ang II的情况下,用心房利钠肽(ANP)和/或一氧化氮(NO)供体S-亚硝基-N-乙酰青霉胺(SNAP)刺激细胞。通过放射免疫测定法(RIA)测定cGMP的合成。单独使用ANP或SNAP可增加足细胞中cGMP的合成,尽管除非培养基中存在Ang II,否则这些作用不会叠加。Ang II抑制ANP依赖性cGMP的合成,而SNAP依赖性cGMP的产生不受影响。这些作用可被Ang II受体(AT)的非特异性拮抗剂沙拉新阻止。相反,AT2受体的特异性抑制剂PD123319增强了对ANP依赖性的抑制作用,并增强了NO依赖性cGMP的产生。丙磺舒是一种抑制cGMP从细胞中排出的抑制剂,它抑制了ANP和SNAP产生的cGMP。我们得出结论,培养的足细胞中cGMP的合成受血管紧张素II调节,并且两种起相反作用的受体AT1和AT2参与了这一效应。此外,细胞内积累的cGMP可能会内在地抑制cGMP的产生。