Mussoni L, Riganti M, Acero R, Erroi A, Conforti G, Mantovani A, Donati M B
Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.
Int J Cancer. 1988 Feb 15;41(2):227-30. doi: 10.1002/ijc.2910410212.
The fibrinolytic activity of cancer cells has been repeatedly implicated in mechanisms of local spread and tumour invasiveness. Mononuclear phagocytes associated with solid tumours might also contribute to fibrin dissolution at the tumour/host interface through the expression of plasminogen activator (PA) activity. We have investigated the PA activity of tumour-associated macrophages (TAM) from 4 transplanted murine tumours in syngeneic hosts; peritoneal macrophages (native and thioglycolate-elicited) from both tumour-bearing and control animals were studied as reference cells. TAM from 3 tumours (MSV, mFS6, MN/MCAI) had basal levels of PA activity (20% plasminogen-independent) comparable to or higher than those of thioglycolate-elicited peritoneal macrophages from the same tumour-bearing animals. TAM isolated from 1 tumour (MS2) had a PA which was very low (60% plasminogen-independent), but higher than the activity of unstimulated peritoneal macrophages. Molecular analysis of PA by SDS-PAGE electrophoresis and fibrin autography revealed in all macrophages a single species having an apparent MW of 48 kDA. It thus appears that, in some experimental neoplasms, tumour cell vicinity may represent an in vivo stimulus for macrophage PA expression.
癌细胞的纤溶活性一直被认为与局部扩散和肿瘤侵袭机制有关。与实体瘤相关的单核吞噬细胞也可能通过纤溶酶原激活物(PA)活性的表达,在肿瘤/宿主界面促进纤维蛋白溶解。我们研究了同基因宿主中4种移植性小鼠肿瘤的肿瘤相关巨噬细胞(TAM)的PA活性;来自荷瘤动物和对照动物的腹膜巨噬细胞(天然的和经巯基乙酸盐诱导的)作为参照细胞进行研究。来自3种肿瘤(MSV、mFS6、MN/MCAI)的TAM的PA基础活性水平(20%不依赖纤溶酶原)与来自同一荷瘤动物经巯基乙酸盐诱导的腹膜巨噬细胞相当或更高。从1种肿瘤(MS2)分离的TAM的PA活性非常低(60%不依赖纤溶酶原),但高于未刺激的腹膜巨噬细胞的活性。通过SDS-PAGE电泳和纤维蛋白自显影对PA进行分子分析,结果显示所有巨噬细胞中均有一种表观分子量为48 kDa的单一蛋白条带。因此,在某些实验性肿瘤中,肿瘤细胞附近可能是巨噬细胞PA表达的一种体内刺激因素。