Salonen V, Aho H, Röyttä M, Peltonen J
Department of Medical Biochemistry, University of Turku, Finland.
Acta Neuropathol. 1988;75(4):331-6. doi: 10.1007/BF00687785.
Schwann cells and endoneurial fibroblast-like cells were quantitated for 30 weeks in both nonregenerating and freely regenerating, transected rat sciatic nerve. Immunocytochemical recognition of S-100 protein was used as a marker for Schwann cells and other immunocytochemical and histological methods in the differentiation of S-100 protein-negative endoneurial cells in cross sections of the distal stump 10 mm distal to the site of transection. A marked increase in the total number of cells was observed during the first 4 weeks after the injury in both operative groups. The quantitative relationships between cell populations remained essentially the same as in normal nerves, although the proliferation of the S-100 protein-negative cell population was proportionately slightly stronger when compared to the number of these cells in normal nerves. After the initial proliferation, a gradual decrease occurred in the total number of cells per cross section. This was most marked in the non-regenerating nerves, whereas in the regenerating nerves the decrease in cell number ceased at 16 weeks. The number of Schwann cells was 3.5 times as high as in the control nerves in this phase. The method used in the present study is less laborious than morphometry employing electron microscopy. Furthermore, electron microscopic characteristics of endoneurial cells are not always reliable after nerve trauma, because normal anatomical relationships have become disturbed. This study demonstrates that S-100 protein immunocytochemistry is useful in the study of traumatic lesions of peripheral nerve.
在未再生和自由再生的横断大鼠坐骨神经中,对施万细胞和神经内膜成纤维样细胞进行了30周的定量研究。使用S-100蛋白的免疫细胞化学识别作为施万细胞的标志物,并采用其他免疫细胞化学和组织学方法,对横断部位远侧10mm处远侧残端横断面中S-100蛋白阴性的神经内膜细胞进行鉴别。在两个手术组中,损伤后的前4周均观察到细胞总数显著增加。尽管与正常神经中这些细胞的数量相比,S-100蛋白阴性细胞群体的增殖略有增强,但细胞群体之间的定量关系与正常神经基本相同。初始增殖后,每个横断面的细胞总数逐渐减少。这在未再生神经中最为明显,而在再生神经中,细胞数量的减少在16周时停止。在此阶段,施万细胞的数量是对照神经中的3.5倍。本研究中使用的方法比采用电子显微镜的形态计量学方法省力。此外,神经损伤后神经内膜细胞的电子显微镜特征并不总是可靠的,因为正常的解剖关系已经受到干扰。本研究表明,S-100蛋白免疫细胞化学在外周神经创伤性病变的研究中是有用的。