Griffin J W, Drucker N, Gold B G, Rosenfeld J, Benzaquen M, Charnas L R, Fahnestock K E, Stocks E A
J Neurosci. 1987 Mar;7(3):682-99. doi: 10.1523/JNEUROSCI.07-03-00682.1987.
This study examined Schwann cell behavior during paranodal demyelination induced by beta,beta'-iminodipropionitrile (IDPN). The stimuli for Schwann cell proliferation, extensively studied in vitro, are less well understood in vivo. Most in vivo systems previously used to examine Schwann cell proliferation in disease are dominated by loss of internodal myelin sheaths. As used in this study, IDPN administration produces neurofilamentous axonal swellings and paranodal demyelination, without segmental demyelination or fiber degeneration. We asked whether Schwann cells would proliferate following the restricted paranodal demyelination that accompanies the axonal swellings, and if so what the sources and distributions of new Schwann cells might be. IDPN was given as a single large dose (2 ml/kg) to 21-d-old rats. Neurofilamentous axonal swellings formed in the proximal regions of motor axons, reaching their greatest enlargement in the root exit zone 8 d after IDPN administration. These swellings subsequently migrated distally down the nerves at rates approaching 1 mm/d. The axonal enlargement was consistently associated with displacement of the myelin sheath attachment sites into internodal regions, and consequent paranodal demyelination. This stage was associated with perikaryal changes, including nucleolar enlargement, "girdling" of the perikaryon, and formation of attenuated stalks separating the perinuclear region from the external cytoplasmic collar. Schwann cells proliferated abundantly during this stage. Daughter Schwann cells migrated within the endoneurial space (outside the nerve fiber basal laminae) to overlie the demyelinated paranodes of swollen nerve fibers. In these regions, local proliferation of Schwann cells continued, resulting in large paranodal clusters of Schwann cells. As the axonal calibers subsequently returned to normal, the outermost myelin lamellae of the original internodes returned to their paranodal attachment sites and the supernumerary Schwann cells disappeared. Formation of short internodes, segmental demyelination, and nerve fiber loss were rare phenomena. These results indicate that paranodal demyelination is a sufficient stimulus to excite abundant Schwann cell proliferation; neither internodal demyelination nor myelin breakdown is a necessary stimulus for mitosis. The 3H-thymidine incorporation studies indicated that the sources of new Schwann cells included markedly increased division of the Schwann cells of unmyelinated fibers and, as they formed, supernumerary Schwann cells. In addition, there were rare examples of 3H-thymidine incorporation by Schwann cells associated with myelinated nerve fibers.(ABSTRACT TRUNCATED AT 400 WORDS)
本研究检测了β,β'-亚氨基二丙腈(IDPN)诱导的结旁脱髓鞘过程中雪旺细胞的行为。在体外被广泛研究的雪旺细胞增殖刺激因素,在体内却了解较少。以前用于研究疾病中雪旺细胞增殖的大多数体内系统,主要是节间髓鞘的丧失。在本研究中,给予IDPN后会产生神经丝轴突肿胀和结旁脱髓鞘,而无节段性脱髓鞘或纤维变性。我们询问雪旺细胞是否会在伴随轴突肿胀的局限性结旁脱髓鞘后增殖,如果会,新雪旺细胞的来源和分布可能是什么。将IDPN以单次大剂量(2 ml/kg)给予21日龄大鼠。运动轴突近端区域形成神经丝轴突肿胀,在给予IDPN后8天在神经根出口区达到最大程度的增大。这些肿胀随后以接近1 mm/d的速度向神经远端迁移。轴突增大始终伴随着髓鞘附着位点向节间区域的移位,以及随之而来的结旁脱髓鞘。这个阶段伴随着胞体变化,包括核仁增大、胞体“束带化”,以及形成将核周区域与外部细胞质环分隔开的变细的柄。在此阶段雪旺细胞大量增殖。子代雪旺细胞在内神经间隙(神经纤维基膜外)内迁移,覆盖肿胀神经纤维的脱髓鞘结旁区。在这些区域,雪旺细胞继续局部增殖,导致结旁出现大量雪旺细胞簇。随着轴突直径随后恢复正常,原始节间的最外层髓鞘板回到其结旁附着位点,多余的雪旺细胞消失。形成短节间、节段性脱髓鞘和神经纤维丢失是罕见现象。这些结果表明,结旁脱髓鞘是刺激雪旺细胞大量增殖的充分因素;节间脱髓鞘和髓鞘崩解都不是有丝分裂的必要刺激因素。3H-胸腺嘧啶核苷掺入研究表明,新雪旺细胞的来源包括无髓纤维雪旺细胞的显著增加的分裂,以及多余雪旺细胞的形成。此外,有罕见的例子显示与有髓神经纤维相关的雪旺细胞掺入3H-胸腺嘧啶核苷。(摘要截断于400字)