Ooi B S, MacCarthy E P, Weiss M A, Hsu A, Ooi Y M
Department of Internal Medicine, University of Cincinnati College of Medicine, OH.
J Lab Clin Med. 1987 Oct;110(4):466-74.
Conditioned media of cultured mouse mesangial cells (possessing microfilaments) were shown to contain a factor that stimulated splenic monocytes-macrophages and blood monocytes to replicate. Replicated cells were shown to express MAC-1 antigen as demonstrated by immunofluorescence with anti-MAC 1 and to possess Fc receptors as evidenced by their capacity to ingest sensitized erythrocytes. Preliminary characterization revealed the following characteristics: by Amicon ultrafiltration, fractions greater than 100,000 daltons were shown to have biologic activity; chromatofocusing of these active fractions revealed a peak of activity associated with fractions having pH 4; heating to 100 degrees C for 10 minutes abolished almost all activity, whereas trypsin treatment was without effect. The observations suggest a mechanism by which mesangial cells may modulate the proliferation of monocytes-macrophages that infiltrate the glomerulus in glomerulonephritis.
培养的小鼠系膜细胞(含有微丝)的条件培养基显示含有一种刺激脾单核细胞-巨噬细胞和血液单核细胞增殖的因子。复制的细胞经抗MAC-1免疫荧光证实表达MAC-1抗原,且因其摄取致敏红细胞的能力证明具有Fc受体。初步特性分析显示以下特征:通过Amicon超滤,大于100,000道尔顿的级分具有生物活性;这些活性级分的色谱聚焦显示活性峰与pH 4的级分相关;加热至100℃10分钟几乎消除了所有活性,而胰蛋白酶处理则无作用。这些观察结果提示了一种系膜细胞可能调节肾小球肾炎中浸润肾小球的单核细胞-巨噬细胞增殖的机制。