Hall S M
Department of Anatomy, United Medical and Dental Schools of Guy's Hospital, London.
Neuropathol Appl Neurobiol. 1989 Nov-Dec;15(6):513-29. doi: 10.1111/j.1365-2990.1989.tb01251.x.
Mammalian peripheral nerve fibres can regenerate after injury. Repair is most likely to succeed if axons are simply crushed or have only a very short (less than 0.5 cm) interstump gap to cross and most likely to fail if the interstump gap is long (greater than 1 cm) and associated with soft tissue damage. Whereas reactive axonal sprouting appears to be an intrinsic neuronal response to injury, the subsequent organization of the axonal sprouts, in particular their orderly outgrowth in minifascicles towards a distant distal stump does not occur unless Schwann cells are present. During the injury response, Schwann cells proliferate; co-migrate with regrowing axons (when the proximal stump is separated from the distal stump); respond to axonal cues by transient upregulation or re-expression of molecules which provide a favourable substrate for axonal extension; and attract bundles of regrowing axons and their associated Schwann cells across interstump gaps up to 1 cm in length. Recruited macrophages remove myelin debris from the Schwann cell tubes; they probably interact with Schwann cells in other ways during the injury response, e.g. by presenting mitogens and cytokines.
哺乳动物的外周神经纤维在损伤后能够再生。如果轴突只是被挤压,或者轴突间的断端间隙非常短(小于0.5厘米),那么修复最有可能成功;而如果断端间隙很长(大于1厘米)并且伴有软组织损伤,修复则最有可能失败。虽然反应性轴突发芽似乎是神经元对损伤的一种内在反应,但除非有施万细胞存在,否则轴突发芽的后续组织形成,尤其是它们以小束状向远处的远侧断端有序生长的过程不会发生。在损伤反应过程中,施万细胞会增殖;与再生轴突共同迁移(当近端断端与远端断端分离时);通过短暂上调或重新表达为轴突延伸提供有利底物的分子来响应轴突信号;并吸引再生轴突束及其相关的施万细胞穿过长达1厘米的断端间隙。被招募的巨噬细胞会清除施万细胞管中的髓磷脂碎片;它们在损伤反应过程中可能还会以其他方式与施万细胞相互作用,例如通过呈现促细胞分裂剂和细胞因子。