Festoff B W, Hantaï D, Soria J, Thomaïdis A, Soria C
J Cell Biol. 1986 Oct;103(4):1415-21. doi: 10.1083/jcb.103.4.1415.
Analyses were made of the fibrinolytic, plasminogen-activating system in skeletal muscle to determine if a regulating influence of the nerve could be detected on these enzymes. Young male mice underwent right sciatic neurectomy. Extracts were prepared from denervated muscle at 2-17 d after axotomy and compared with controls. Using a cascade-style biochemical assay (Rånby, M., B. Norrman, and P. Wallén, 1982, Thromb. Res., 27:743-748) we found that low levels of plasminogen activator (PA) were present in adult, innervated mouse muscle, but that denervation resulted in a marked time-dependent increase in enzyme activity. Qualitative separation showed an eightfold increase in urokinase-like PA with moderate elevation of tissue PA activity after 10 d. Fibrin zymography (Granelli-Piperno, A., and E. Reich, 1978, J. Exp. Med., 148:223-234) revealed clear zones of lysis corresponding to molecular masses of 48 kD for urokinase-like PA and 75 kD for tissue PA, consistent with the molecular masses found for these enzymes in other tissues of the mouse (Danø, K., P. A. Andreasen, J. Grøndahl-Hansen, P. Kristensen, L. S. Nielsen, and L. Skriver, 1985, Adv. Cancer Res., 44:139-266). In other studies we have shown that PA-activated plasmin readily attacks critical adhesive basement membrane molecules. The present results indicate that enzymes involved in plasminogen activation, particularly urokinase-like PA, rapidly increase after axotomy, suggesting they may have a role early in muscle denervation. Similar alterations in PA activity might underlie the elimination of polyneuronal innervation during mammalian muscle development. Certain neuromuscular diseases may also involve activation of these enzymes, resulting in degradation of basement membrane zone components and, therefore, warrant further study.
对骨骼肌中的纤维蛋白溶解、纤溶酶原激活系统进行了分析,以确定是否能检测到神经对这些酶的调节作用。年轻雄性小鼠接受右侧坐骨神经切除术。在轴突切断术后2 - 17天,从去神经支配的肌肉中制备提取物,并与对照组进行比较。使用一种级联式生化检测方法(Rånby, M., B. Norrman, and P. Wallén, 1982, Thromb. Res., 27:743 - 748),我们发现成年、有神经支配的小鼠肌肉中存在低水平的纤溶酶原激活剂(PA),但去神经支配导致酶活性出现明显的时间依赖性增加。定性分离显示,10天后,尿激酶型PA增加了8倍,组织PA活性适度升高。纤维蛋白酶谱分析(Granelli-Piperno, A., and E. Reich, 1978, J. Exp. Med., 148:223 - 234)显示,对应于尿激酶型PA分子量48 kD和组织PA分子量75 kD的清晰溶解区,这与在小鼠其他组织中发现的这些酶的分子量一致(Danø, K., P. A. Andreasen, J. Grøndahl-Hansen, P. Kristensen, L. S. Nielsen, and L. Skriver, 1985, Adv. Cancer Res., 44:139 - 266)。在其他研究中,我们已经表明PA激活的纤溶酶很容易攻击关键的黏附性基底膜分子。目前的结果表明,参与纤溶酶原激活的酶,特别是尿激酶型PA,在轴突切断后迅速增加,表明它们可能在肌肉去神经支配早期发挥作用。PA活性的类似改变可能是哺乳动物肌肉发育过程中多神经元支配消除的基础。某些神经肌肉疾病也可能涉及这些酶的激活,导致基底膜区成分的降解,因此值得进一步研究。