Tsirka S E, Bugge T H, Degen J L, Strickland S
Department of Pharmacology, University Medical Center at Stony Brook, Stony Brook, NY 11794-8651, USA.
Proc Natl Acad Sci U S A. 1997 Sep 2;94(18):9779-81. doi: 10.1073/pnas.94.18.9779.
Mice deficient for plasminogen exhibit a variety of pathologies, all of which examined to date are reversed when the animals are also made fibrin(ogen) deficient. These results suggested that the predominant, and perhaps exclusive, physiological role of plasminogen is clearance of fibrin. Plasminogen-deficient mice also display resistance to excitotoxin-induced neurodegeneration, in contrast with wild-type mice, which are sensitive. Based on the genetic interaction between plasminogen and fibrinogen, we investigated whether resistance to neuronal cell death in the plasminogen-deficient mice is dependent on fibrin(ogen). Unexpectedly, mice lacking both plasminogen and fibrinogen are resistant to neurodegeneration to levels comparable to plasminogen-deficient mice. Therefore, plasmin acts on substrates other than fibrin during experimental neuronal degeneration, and may function similarly in other pathological settings in the central nervous system.
缺乏纤溶酶原的小鼠表现出多种病理状况,迄今为止所检测的所有这些状况在动物同时缺乏纤维蛋白(原)时都会逆转。这些结果表明,纤溶酶原的主要生理作用(或许也是唯一作用)是清除纤维蛋白。与敏感的野生型小鼠相比,缺乏纤溶酶原的小鼠对兴奋性毒素诱导的神经退行性变也表现出抗性。基于纤溶酶原和纤维蛋白原之间的基因相互作用,我们研究了缺乏纤溶酶原的小鼠对神经元细胞死亡的抗性是否依赖于纤维蛋白(原)。出乎意料的是,同时缺乏纤溶酶原和纤维蛋白原的小鼠对神经退行性变的抗性水平与缺乏纤溶酶原的小鼠相当。因此,在实验性神经元变性过程中,纤溶酶作用于纤维蛋白以外的底物,并且在中枢神经系统的其他病理情况下可能发挥类似作用。