Matsumoto K
Second Department of Internal Medicine, Nihon University School of Medicine, Tokyo, Japan.
Am J Nephrol. 1989;9(6):488-94. doi: 10.1159/000168018.
The objective of the present work was to characterize some aspects of interleukin-1 (IL-1) production by nephritic glomeruli after stimulation with bacterial lipopolysaccharide (LPS). Freshly isolated glomeruli from rats with an accelerated autologous form of nephrotoxic serum nephritis (NTSN) were incubated for 24 h in the presence of LPS. The modified NTSN was produced by an intravenous injection of nephrotoxic serum (NTS) into the rats which had been previously immunized with rabbit IgG and Freund's complete adjuvant. The glomerular cultures of the NTSN rats were found to release significantly increased amounts of IL-1 after LPS stimulation when compared to the values obtained with normal controls and the other control group, consisting of preimmunized rats (rabbit IgG), then given normal rabbit globulin instead of NTS. To block the effect of prostaglandins on the IL-1 assay, we cultured the glomeruli with the addition of indomethacin and assayed IL-1 activity in the culture supernatants. The use of indomethacin resulted in a further increase in IL-1 production. The administration of a rabbit anti-rat macrophage serum reduced the production of IL-1 activity in the NTSN rats. Our findings support the notion that at least in NTSN rats activated macrophages are present and probably account for their increased IL-1 activity. This description of IL-1 activity produced by LPS-stimulated nephritic glomeruli may introduce a new element to the early events leading to glomerular inflammation.
本研究的目的是表征经细菌脂多糖(LPS)刺激后,肾炎性肾小球白细胞介素-1(IL-1)产生的某些方面。从患有加速型自体肾毒性血清肾炎(NTSN)的大鼠中新鲜分离的肾小球,在LPS存在下孵育24小时。改良的NTSN是通过将肾毒性血清(NTS)静脉注射到先前用兔IgG和弗氏完全佐剂免疫的大鼠中产生的。与正常对照组以及由预先免疫的大鼠(兔IgG)组成的另一对照组(随后给予正常兔球蛋白而非NTS)相比,发现NTSN大鼠的肾小球培养物在LPS刺激后释放出显著增加的IL-1量。为了阻断前列腺素对IL-1测定的影响,我们在添加吲哚美辛的情况下培养肾小球,并测定培养上清液中的IL-1活性。使用吲哚美辛导致IL-1产生进一步增加。给予兔抗大鼠巨噬细胞血清可降低NTSN大鼠中IL-1活性的产生。我们的研究结果支持这样一种观点,即至少在NTSN大鼠中存在活化的巨噬细胞,并且可能是其IL-1活性增加的原因。对LPS刺激的肾炎性肾小球产生的IL-1活性的这种描述可能为导致肾小球炎症的早期事件引入一个新的因素。