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引导成年哺乳动物感觉轴突再生。

Guiding adult Mammalian sensory axons during regeneration.

作者信息

Webber Christine A, Xu Yongqin, Vanneste Kimberly J, Martinez Jose A, Verge Valerie M K, Zochodne Douglas W

机构信息

Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.

出版信息

J Neuropathol Exp Neurol. 2008 Mar;67(3):212-22. doi: 10.1097/NEN.0b013e3181654972.

Abstract

Misdirection of axons after nerve injury impairs successful regeneration of adult neurons. Investigations of axon guidance in development have provided an understanding of pathfinding, but their relevance to regenerating adult axons is unclear. We investigated adult mammalian axon guidance during regeneration after peripheral nerve injury and focused on the effects of the prototypic guidance molecule nerve growth factor (NGF). Adult rat sensory neurons from dorsal root ganglia that expressed the NGF receptor tropomyosin-related kinase A (trkA) were presented with a point source of NGF in vitro. Naive trkA neurons had no net turning response to NGF, but if they had been preconditioned by a peripheral nerve transection in vivo before culturing, their growth cones were attracted toward the NGF gradient. A laminin substrate was required for this behavior and an anti-trkA antibody interrupted turning. These data demonstrate that injured adult mammalian axons can be guided as they regenerate. Moreover, despite the downregulation of trkA mRNA and protein levels within the dorsal root ganglion after injury, sensory neurons retain and increase trkA protein at the injury site where the regenerating axons are found. This may enhance the axonal response to NGF and allow guidance along an NGF gradient created in vivo in the distal nerve stump.

摘要

神经损伤后轴突的错误导向会损害成年神经元的成功再生。对发育过程中轴突导向的研究有助于理解路径寻找,但它们与成年轴突再生的相关性尚不清楚。我们研究了成年哺乳动物周围神经损伤后再生过程中的轴突导向,并聚焦于典型导向分子神经生长因子(NGF)的作用。在体外,将表达NGF受体原肌球蛋白相关激酶A(trkA)的成年大鼠背根神经节感觉神经元置于NGF点源处。未接触过NGF的trkA神经元对NGF没有净转向反应,但如果在培养前在体内进行过周围神经横断预处理,其生长锥会被吸引向NGF梯度。这种行为需要层粘连蛋白底物,且抗trkA抗体可阻断转向。这些数据表明,受损的成年哺乳动物轴突在再生时可以被引导。此外,尽管损伤后背根神经节内trkA mRNA和蛋白水平下调,但感觉神经元在发现再生轴突的损伤部位保留并增加了trkA蛋白。这可能增强轴突对NGF的反应,并允许沿着在体内远端神经残端形成的NGF梯度进行导向。

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