Jensen B L, Lehle U, Müller M, Wagner C, Kurtz A
Physiologisches Institut der Universität Regensburg, D-93040 Regensburg, Germany.
Pflugers Arch. 1998 Oct;436(5):673-8. doi: 10.1007/s004240050688.
Cardiovascular effects of inflammatory interleukins (IL) have been suggested to be mediated by the renin-angiotensin system in vivo. To address the direct cellular effect of IL, we examined the influence of IL-1beta on renin secretion and renin mRNA in cultures of mouse juxtaglomerular granular (JG) cells and in the mouse tumor cell line As4.1, which expresses renin mRNA. Renin mRNA levels and secretion of active renin were not significantly changed by IL-1beta in native JG cells. Activation of adenylyl cyclase by forskolin increased renin secretion and renin mRNA levels three- and fivefold, respectively. These stimulatory responses to forskolin were not altered by IL-1beta. In contrast to native JG cells, renin mRNA abundance was markedly suppressed by IL-1beta in As4.1 cells, whereas secretion of active renin and the stability of renin mRNA were not changed. In As4.1 cells forskolin did not change renin secretion or renin mRNA abundance in the absence or in the presence of IL-1beta. These findings suggest that IL-1beta has no direct influence on renin secretion and renin mRNA abundance at the level of native JG cells.
炎症性白细胞介素(IL)对心血管系统的影响在体内被认为是由肾素-血管紧张素系统介导的。为了研究IL的直接细胞效应,我们检测了IL-1β对小鼠肾小球旁颗粒(JG)细胞培养物以及表达肾素mRNA的小鼠肿瘤细胞系As4.1中肾素分泌和肾素mRNA的影响。在天然JG细胞中,IL-1β并未显著改变肾素mRNA水平和活性肾素的分泌。福斯可林激活腺苷酸环化酶分别使肾素分泌和肾素mRNA水平增加了三倍和五倍。IL-1β并未改变这些对福斯可林的刺激反应。与天然JG细胞不同,在As4.1细胞中,IL-1β显著抑制了肾素mRNA丰度,而活性肾素的分泌和肾素mRNA的稳定性并未改变。在As4.1细胞中,无论有无IL-1β,福斯可林均未改变肾素分泌或肾素mRNA丰度。这些发现表明,在天然JG细胞水平上,IL-1β对肾素分泌和肾素mRNA丰度没有直接影响。