雪旺细胞
再生(生物学)
轴突
低亲和力神经生长因子受体
神经导管
周围神经损伤
病理
生物
神经营养素
神经损伤
再髓鞘化
增殖细胞核抗原
细胞生物学
神经科学
医学
受体
髓鞘
免疫组织化学
内科学
中枢神经系统
作者
Masaki Kobayashi,Satoru Ishibashi,Hiroyuki Tomimitsu,Takanori Yokota,Hidehiro Mizusawa
标识
DOI:10.1097/nen.0b013e318257fe7b
摘要
Schwann cells exhibit a high degree of plasticity in adult peripheral nerves after mechanical injury; they have, therefore, been implicated in promoting nerve regeneration. However, Schwann cell behavior after ischemic injury has not yet been elucidated. To determine how Schwann cell plasticity may contribute to recovery from ischemic neuropathy, we used a rat model in which ischemia was induced in the tibial nerve by a 5-hour occlusion of the supplying arteries. Proliferation of immature Schwann cells that emerged in the injured nerve was evaluated by double immunostaining for the p75 neurotrophin receptor and proliferating cell nuclear antigen. The number of proliferating cell nuclear antigen/p75 neurotrophin receptor double-positive cells increased significantly in 1 to 2 weeks after ischemia and subsequently decreased by 4 weeks. During this time, the postmitotic Schwann cells differentiated into mature cells, as demonstrated with bromodeoxyuridine incorporation, which facilitated axon guidance and subsequent axon remyelination. These results suggest the emergence and proliferation of immature Schwann cells that contribute to nerve regeneration after ischemic injury. The manipulation of this population of proliferating immature Schwann cells may be a useful strategy for treating ischemic peripheral neuropathy.
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