Scalabrino G, Tredici G, Buccellato F R, Manfridi A
Institute of General Pathology, Faculty of Medicine, University of Milan, Italy.
J Neuropathol Exp Neurol. 2000 Sep;59(9):808-14. doi: 10.1093/jnen/59.9.808.
In order to get further evidence for a mandatory involvement of epidermal growth factor (EGF) in the neutrophic action of vitamin B12 (cobalamin (Cbl)) in the central nervous system (CNS) of the rat, we observed the effects of repeated intracerebroventricular (ICV) microinjections of EGF in rats made Cbl-deficient through total gastrectomy. Morphometric analysis demonstrated a significant reduction in both intramyelinic and interstitial edema in the white matter of the spinal cord (SC) of totally gastrectomized (TGX) rats after treatment. Intramyelinic and interstitial edema are characteristic of Cbl-deficient central neuropathy in the rat. Similar lesions were also present in SC white matter of rats treated with repeated ICV microinjections of specific anti-EGF antibodies without any modification in their Cbl status. These results, together with those of a previous study showing the cessation of EGF synthesis in the CNS of TGX rats, demonstrate that: a) EGF is necessarily involved in the signaling pathway of Cbl in the rat CNS; and b) the lack of a neurotrophic growth factor EGF, and not the mere withdrawal of Cbl, causes or at least contributes to neurodegenerative Cbl-deficient central neuropathy.
为了获得进一步证据,证明表皮生长因子(EGF)在大鼠中枢神经系统(CNS)中对维生素B12(钴胺素(Cbl))的神经营养作用具有强制性参与,我们观察了对通过全胃切除术造成Cbl缺乏的大鼠反复进行脑室内(ICV)微量注射EGF的效果。形态计量学分析表明,治疗后全胃切除(TGX)大鼠脊髓(SC)白质中的髓鞘内和间质水肿均显著减轻。髓鞘内和间质水肿是大鼠Cbl缺乏性中枢神经病变的特征。在Cbl状态未发生任何改变的情况下,用特异性抗EGF抗体反复进行ICV微量注射处理的大鼠的SC白质中也存在类似病变。这些结果,连同先前一项研究显示TGX大鼠中枢神经系统中EGF合成停止的结果,表明:a)EGF必然参与大鼠中枢神经系统中Cbl的信号传导途径;b)神经营养生长因子EGF的缺乏,而不仅仅是Cbl的缺乏,导致或至少促成了神经退行性Cbl缺乏性中枢神经病变。