Martin T J, Allan E H, Fukumoto S
St. Vincent's Institute of Medical Research, Melbourne, Victoria, Australia.
Growth Regul. 1993 Dec;3(4):209-14.
The neutral protease, plasmin, is generated by plasminogen activators, and is ascribed an important role in several physiological and pathological circumstances characterized by tissue remodelling and cell motility. The two types of plasminogen activator, tissue-type (tPA) and urokinase-type (uPA), are produced by osteoblasts, as is the specific PA inhibitor, PAI-1. Some hormones which activate bone resorption increase PA activity produced by osteoblasts, by decreasing the production of PAI-1. The increased PA activity has been suggested to facilitate bone resorption by activating latent collagenase, thus preparing the bone surface for osteoclastic resorption. Targeted and regulated production of plasmin might also contribute to the coupling of bone formation to resorption, by activating latent TGF beta in bone, and activating IGF-1 by freeing it from association with inhibitory binding protein. TGF beta itself is a powerful inhibitor of PA activity, an effect achieved by enhancing mRNA and protein for PAI-1. Thus the PA system is a potentially important regulatory system in bone remodelling, whose local activity is controlled through concerted actions of hormones and locally generated growth factors and cytokines.
中性蛋白酶——纤溶酶,由纤溶酶原激活剂生成,在以组织重塑和细胞运动为特征的多种生理和病理情况下发挥重要作用。两种类型的纤溶酶原激活剂,即组织型(tPA)和尿激酶型(uPA),与特异性PA抑制剂PAI - 1一样,均由成骨细胞产生。一些激活骨吸收的激素通过减少PAI - 1的产生来增加成骨细胞产生的PA活性。PA活性增加被认为可通过激活潜在的胶原酶来促进骨吸收,从而为破骨细胞的吸收作用准备骨表面。纤溶酶的靶向性和调节性产生也可能通过激活骨中潜在的转化生长因子β(TGFβ)以及使胰岛素样生长因子-1(IGF - 1)从与抑制性结合蛋白的结合中释放出来从而激活IGF - 1,来促进骨形成与吸收的偶联。TGFβ本身是PA活性的强效抑制剂,这一作用是通过增强PAI - 1的mRNA和蛋白质水平来实现的。因此,PA系统是骨重塑中一个潜在的重要调节系统,其局部活性通过激素以及局部产生的生长因子和细胞因子的协同作用来控制。