Conti G, Stoll G, Scarpini E, Baron P L, Bianchi R, Livraghi S, Scarlato G
Institute of Neurology, Dino Ferrari Center, University of Milan, IRCCS Ospedale Maggiore Policlinico, Italy.
Exp Neurol. 1997 Jul;146(1):206-11. doi: 10.1006/exnr.1997.6521.
In this study we examined the expression of the neurotrophin receptor p75 (p75NTR) and the activation of macrophages in the sciatic nerve of rats at different time points after the induction of diabetes with streptozotocin (STZ). Northern blot and immunocytochemical analysis showed that p75NTR was not detectable in the sciatic nerve by Week 2 after STZ treatment. At this time, single nerve fiber immunostaining using ED1 monoclonal antibody revealed that active macrophages were infiltrating the endoneurium, which had a normal morphological aspect. By Weeks 5 and 15 p75NTR mRNA and protein were induced in the endoneurium of diabetic animals. Immunocytochemical analysis of teased single nerve fibers showed that p75NTR protein was distributed uniformly along isolated fibers with no pathological evidence of axonal degeneration or myelin disruption. At this time, cells of the phagocyte lineage had already disappeared from the nerve. These data show that during experimental diabetic neuropathy, the endoneurial induction of p75NTR is localized along isolated nerve fibers showing no morphological alterations, and in time, follows the recruitment of active macrophages in the nerve, suggesting that these cells, directly or through their products, can influence p75NTR induction. This process might play an important role in STZ diabetic neuropathy, as a response to decreased levels of neurotrophins such as NGF and promoting nerve regeneration in the early phases of the disease.
在本研究中,我们检测了用链脲佐菌素(STZ)诱导糖尿病后不同时间点大鼠坐骨神经中神经营养因子受体p75(p75NTR)的表达以及巨噬细胞的活化情况。Northern印迹和免疫细胞化学分析显示,STZ处理后第2周时在坐骨神经中检测不到p75NTR。此时,使用ED1单克隆抗体进行的单神经纤维免疫染色显示,活跃的巨噬细胞正在浸润形态正常的神经内膜。到第5周和第15周时,糖尿病动物的神经内膜中诱导出了p75NTR mRNA和蛋白。对 teased 单神经纤维的免疫细胞化学分析表明,p75NTR蛋白沿分离的纤维均匀分布,没有轴突变性或髓鞘破坏的病理学证据。此时,吞噬细胞系的细胞已从神经中消失。这些数据表明,在实验性糖尿病性神经病变期间,神经内膜中p75NTR的诱导沿着未显示形态改变的分离神经纤维定位,并且随着时间的推移,跟随神经中活跃巨噬细胞的募集,这表明这些细胞直接或通过其产物可影响p75NTR的诱导。这一过程可能在STZ糖尿病性神经病变中起重要作用,作为对诸如NGF等神经营养因子水平降低的一种反应,并在疾病早期促进神经再生。