Mattana J, Sankaran R T, Singhal P C
Department of Medicine, Long Island Jewish Medical Center, New Hyde Park, New York 11042, USA.
Am J Pathol. 1995 Aug;147(2):529-40.
Uptake of immunoglobulin G (IgG) complexes by macrophages (M phi) may play an important role in disease states characterized by increased levels of circulating immune complexes. In sites such as the glomerular mesangium M phi may be subjected to repetitive mechanical strain, although in vitro studies of M phi endocytosis are typically carried out with cells grown on rigid surfaces. We undertook the present study to determine whether repetitive mechanical strain could modulate M phi endocytosis of IgG complexes. IgG complex uptake was significantly diminished in M phi that were subjected to repetitive mechanical strain using parameters corresponding to peak and minimal intraglomerular pressures compared with control, and uptake varied according to the amount of mechanical strain applied. There was no significant difference in surface binding of IgG between M phi subjected to strain and those not. Mechanical strain did not significantly influence the rate of IgG complex degradation. Inhibition of nitric oxide synthase and guanylate cyclase activity did not alter the effect of mechanical strain, although this effect was potentiated by 3-isobutyl-1-methylxanthine (IBMX). Angiotensin II, which has been shown to reduce adenosine 3',5'-cyclic monophosphate (cAMP) production in M phi, significantly attenuated the suppressive effect of mechanical strain on IgG complex uptake as well as another inhibitor of cAMP generation, indomethacin. Enzyme immunoassay demonstrated significantly enhanced levels of cAMP in M phi that were subjected to mechanical strain compared with control, an effect that was potentiated by IBMX and attenuated by angiotensin II and indomethacin. These results demonstrate that repetitive mechanical strain significantly reduces IgG complex uptake by M phi, most likely by enhancing cAMP synthesis. Such an effect might play a significant role in macromolecule handling by M phi in sites in which they are subjected to repetitive mechanical deformation such as the glomerular mesangium.
巨噬细胞摄取免疫球蛋白G(IgG)复合物可能在以循环免疫复合物水平升高为特征的疾病状态中起重要作用。在肾小球系膜等部位,巨噬细胞可能会受到反复的机械应变,尽管巨噬细胞内吞作用的体外研究通常是在生长于刚性表面的细胞上进行的。我们开展本研究以确定反复的机械应变是否能调节巨噬细胞对IgG复合物的内吞作用。与对照组相比,使用对应于肾小球内压力峰值和最小值的参数对巨噬细胞施加反复机械应变后,其对IgG复合物的摄取显著减少,且摄取量随施加的机械应变大小而变化。施加应变的巨噬细胞与未施加应变的巨噬细胞在IgG的表面结合方面无显著差异。机械应变对IgG复合物的降解速率无显著影响。抑制一氧化氮合酶和鸟苷酸环化酶活性并未改变机械应变的作用,尽管3-异丁基-1-甲基黄嘌呤(IBMX)可增强该作用。已证明可降低巨噬细胞中3',5'-环磷酸腺苷(cAMP)生成的血管紧张素II,显著减弱了机械应变对IgG复合物摄取的抑制作用,以及另一种cAMP生成抑制剂吲哚美辛的作用。酶免疫测定表明,与对照组相比,施加机械应变的巨噬细胞中cAMP水平显著升高,该作用被IBMX增强,被血管紧张素II和吲哚美辛减弱。这些结果表明,反复的机械应变显著降低巨噬细胞对IgG复合物的摄取,很可能是通过增强cAMP合成实现的。这种作用可能在巨噬细胞于诸如肾小球系膜等遭受反复机械变形的部位处理大分子的过程中起重要作用。