Wohlwend A, Belin D, Vassalli J D
J Exp Med. 1987 Feb 1;165(2):320-39. doi: 10.1084/jem.165.2.320.
Human monocytes/macrophages produce plasminogen activator-specific inhibitors (PAIs) that form covalent complexes with urokinase-type plasminogen activator (uPA). We have characterized two functionally and antigenically related forms of PAIs produced by resting and phorbol myristate acetate (PMA)-treated U 937 cells: an Mr 40,000 form, presumably nonglycosylated, with a pI of 5.2, that is constitutively synthetized by these cells and that remains predominantly intracellular; a PMA-induced form of heterogeneous Mr (50,000-65,000) with a pI of 4.7, that is preferentially secreted; this PAI is glycosylated with terminal sialic acid residue(s). Biosynthetic labeling experiments demonstrated that both PAIs are synthetized by U 937 cells. They are inactivated upon treatment with propanol, heat, and acid; the covalent and equimolar complexes formed between these PAIs and 125I-uPA are dissociated by ammonium hydroxide, suggesting that the PAIs are linked to uPA via an ester bond. Human peripheral blood monocytes/macrophages also produce the two forms of PAI. These PAIs are clearly different from the main plasma protease inhibitors and they are both antigenically related to the PAI-2 characterized in human placenta.
人单核细胞/巨噬细胞产生纤溶酶原激活物特异性抑制剂(PAIs),这些抑制剂与尿激酶型纤溶酶原激活物(uPA)形成共价复合物。我们已对静息和佛波酯(PMA)处理的U 937细胞产生的两种功能和抗原相关的PAI形式进行了表征:一种分子量为40,000的形式,可能是非糖基化的,pI为5.2,由这些细胞组成性合成,主要保留在细胞内;一种PMA诱导的分子量异质性(50,000 - 65,000)的形式,pI为4.7,优先分泌;这种PAI被末端唾液酸残基糖基化。生物合成标记实验表明,两种PAI均由U 937细胞合成。它们在用丙醇、加热和酸处理后失活;这些PAI与125I - uPA之间形成的共价等摩尔复合物可被氢氧化铵解离,表明PAI通过酯键与uPA相连。人外周血单核细胞/巨噬细胞也产生这两种形式的PAI。这些PAI与主要的血浆蛋白酶抑制剂明显不同,并且它们在抗原上均与在人胎盘中鉴定的PAI - 2相关。