Narita I, Morioka T, Arakawa M, Shimizu F, Oite T
Department of Medicine (II), Niigata University School of Medicine, Japan.
Clin Exp Immunol. 1991 Mar;83(3):497-504. doi: 10.1111/j.1365-2249.1991.tb05668.x.
The present study was conducted to determine the manner in which monocytes increase mesangial matrices, particularly glycosaminoglycans (GAGs) which interact with various other matrix components such as collagens, laminin, fibronectin and lipoproteins. A supernatant of human peripheral blood monocyte cultures activated by lipopolysaccharide (LPS) contains stimulating factors for glycosaminoglycan synthesis in rat mesangial cells (MCs). The culture supernatant in this study was concentrated and fractionated by gel chromatography and the GAG-stimulatory factor was found to have a molecular weight of 10-17 kD. This factor was shown to be present in fractions different from that of IL-1. Gel and ion-exchange chromatography studies of GAGs synthesized by MCs indicated the elution patterns of GAGs in the presence and absence of the monocyte culture supernatant to be essentially the same. Local infiltration of monocytes into the glomerulus, often seen in various types of glomerular injury, may be an important factor in the accumulation of the mesangial matrix.
本研究旨在确定单核细胞增加系膜基质的方式,特别是与各种其他基质成分(如胶原蛋白、层粘连蛋白、纤连蛋白和脂蛋白)相互作用的糖胺聚糖(GAGs)。由脂多糖(LPS)激活的人外周血单核细胞培养上清液含有刺激大鼠系膜细胞(MCs)合成糖胺聚糖的因子。本研究中的培养上清液通过凝胶色谱法进行浓缩和分级分离,发现GAG刺激因子的分子量为10 - 17 kD。该因子显示存在于与白细胞介素-1不同的组分中。对MCs合成的GAGs进行凝胶和离子交换色谱研究表明,在有和没有单核细胞培养上清液的情况下,GAGs的洗脱模式基本相同。在各种类型的肾小球损伤中经常可见单核细胞局部浸润到肾小球中,这可能是系膜基质积累的一个重要因素。