Petricevich V L, Michelacci Y M
Escola Paulista de Medicina, Departamento de Bioquímica, São Paulo, Brazil.
Biochim Biophys Acta. 1990 Jul 12;1053(2-3):135-43. doi: 10.1016/0167-4889(90)90005-x.
Peritoneal macrophages from nude mice were found to be functionally similar to 'activated' macrophages from normal mice. The objective of the present study was to characterize the proteoglycans synthesized and secreted in vitro by peritoneal macrophages isolated from nude and normal Balb/c mice and to investigate the relationship between macrophage 'activation' and changes in the proteoglycan patterns. Macrophages obtained by peritoneal lavage were seeded in Petri dishes. After 2 h incubation at 37 degrees C, the adherent cells (macrophages) were exposed to [35S]sulphate for the biosynthetic labelling of proteoglycans. After incubation, the cell and medium fractions were collected and analysed for proteoglycans and glycosaminoglycans. The glycosaminoglycans were identified and characterized by a combination of agarose gel electrophoresis and enzymatic degradation with specific mucopolysaccharidases. It was shown that 3/4 of the total 35S-labelled glycosaminoglycans were in the extracellular compartment after 24-48 h. The macrophages synthesized dermatan sulphate (68%), chondroitin sulphate (7%) and heparan sulphate (25%). Both cell and medium fractions of normal and nude mouse macrophages contained glycosaminoglycans with the same ratios, although the nude mouse macrophages synthesized 2-fold less glycosaminoglycans than the normal mouse macrophages. Lower levels of 35S-proteoglycans were also obtained from in vitro 'activated' macrophages, but the ratios of dermatan sulphate:chondroitin sulphate: heparan sulphate were altered in these cells as compared to the control. Furthermore, all the 35S-macromolecules found in the extracellular compartment of nude and normal control cells were of proteoglycan nature, in contrast to the medium fractions of 'activated' macrophages, which contain both intact proteoglycans and 'free' glycosaminoglycan chains. These results indicate that, at least as regards the proteoglycans and glycosaminoglycans, the nude mouse macrophages are not identical to the 'activated' macrophages from normal mice.
研究发现,裸鼠的腹腔巨噬细胞在功能上与正常小鼠的“活化”巨噬细胞相似。本研究的目的是对从裸鼠和正常Balb/c小鼠分离的腹腔巨噬细胞在体外合成和分泌的蛋白聚糖进行表征,并研究巨噬细胞“活化”与蛋白聚糖模式变化之间的关系。通过腹腔灌洗获得的巨噬细胞接种于培养皿中。在37℃孵育2小时后,将贴壁细胞(巨噬细胞)暴露于[35S]硫酸盐中,用于蛋白聚糖的生物合成标记。孵育后,收集细胞和培养基部分,并分析其中的蛋白聚糖和糖胺聚糖。通过琼脂糖凝胶电泳和用特定的粘多糖酶进行酶解相结合的方法对糖胺聚糖进行鉴定和表征。结果表明,24 - 48小时后,35S标记的总糖胺聚糖中有3/4存在于细胞外区室。巨噬细胞合成了硫酸皮肤素(68%)、硫酸软骨素(7%)和硫酸乙酰肝素(25%)。正常和裸鼠巨噬细胞的细胞和培养基部分都含有相同比例的糖胺聚糖,尽管裸鼠巨噬细胞合成的糖胺聚糖比正常小鼠巨噬细胞少2倍。从体外“活化”的巨噬细胞中也获得了较低水平的35S - 蛋白聚糖,但与对照相比,这些细胞中硫酸皮肤素:硫酸软骨素:硫酸乙酰肝素的比例发生了改变。此外,裸鼠和正常对照细胞细胞外区室中发现的所有35S - 大分子都是蛋白聚糖性质的,这与“活化”巨噬细胞的培养基部分不同,后者既含有完整的蛋白聚糖,也含有“游离”的糖胺聚糖链。这些结果表明,至少就蛋白聚糖和糖胺聚糖而言,裸鼠巨噬细胞与正常小鼠的“活化”巨噬细胞并不相同。