Hantaï D, Akaaboune M, Verdière-Sahuqué M, Lachkar S, Festoff B W
INSERM U, Paris, France.
C R Seances Soc Biol Fil. 1994;188(5-6):541-52.
It is now well established that some serine proteases, such as plasminogen activators and thrombin, as well as their inhibitors, have roles in the development of both central and peripheral nervous systems. We have shown that muscle plasminogen activators, activated after denervation, were able to digest some components of the muscle basement membrane. We have also shown that several inhibitors of serine proteases were concentrated at the neuromuscular junction. These are protease nexin, I, also called glia-derived nexin, protease nexin II, a secreted form of the beta-amyloid precursor protein (APP), and alpha 1-antichymotrypsine (ACT). These results leads us to propose a model in which serine proteases would favor plasticity of motor nerve endings during neuromuscular development. On the contrary, the inhibitors of serine proteases would act to provide and secure maintenance of the synaptic contact. A dysequilibrium between serine proteases and their inhibitors might underlie one or more motor neuron diseases.
现在已经充分证实,一些丝氨酸蛋白酶,如纤溶酶原激活剂和凝血酶,以及它们的抑制剂,在中枢神经系统和周围神经系统的发育中都发挥着作用。我们已经表明,失神经支配后被激活的肌肉纤溶酶原激活剂能够消化肌肉基底膜的一些成分。我们还表明,几种丝氨酸蛋白酶抑制剂集中在神经肌肉接头处。这些抑制剂包括蛋白酶连接素I(也称为胶质细胞衍生的连接素)、蛋白酶连接素II(β-淀粉样前体蛋白(APP)的一种分泌形式)和α1-抗糜蛋白酶(ACT)。这些结果使我们提出一个模型,即在神经肌肉发育过程中,丝氨酸蛋白酶有利于运动神经末梢的可塑性。相反,丝氨酸蛋白酶抑制剂将起到提供和确保突触接触维持的作用。丝氨酸蛋白酶与其抑制剂之间的失衡可能是一种或多种运动神经元疾病的基础。