Smith D S, Skene J H
Department of Neurobiology, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Neurosci. 1997 Jan 15;17(2):646-58. doi: 10.1523/JNEUROSCI.17-02-00646.1997.
Although maturing neurons undergo a precipitous decline in the expression of genes associated with developmental axon growth, structural changes in axon arbors occur in the adult nervous system under both normal and pathological conditions. Furthermore, some neurons support extensive regrowth of long axons after nerve injury. Analysis of adult dorsal root ganglion (DRG) neurons in culture now shows that competence for distinct types of axon growth depends on different patterns of gene expression. In the absence of ongoing transcription, newly isolated neurons can extend compact, highly branched arbors during the first day in culture. Neurons subjected to peripheral axon injury 2-7 d before plating support a distinct mode of growth characterized by rapid extension of long, sparsely branched axons. A transition from "arborizing" to "elongating" growth occurs in naive adult neurons after approximately 24 hr in culture but requires a discrete period of new transcription after removal of the ganglia from the intact animal. Thus, peripheral axotomy-by nerve crush or during removal of DRGs--induces a transcription-dependent change that alters the type of axon growth that can be executed by these adult neurons. This transition appears to be triggered, in large part, by interruption of retrogradely transported signals, because blocking axonal transport in vivo can elicit competence for elongating growth in many DRG neurons. In contrast to peripheral axotomy, interruption of the centrally projecting axons of DRG neurons in vivo leads to subsequent growth in vitro that is intermediate between "arborizing" and "elongating" growth. This suggests that the transition between these two modes of growth is a multistep process and that individual steps may be regulated separately. These observations together suggest that structural remodeling in the adult nervous system need not involve the same molecular apparatus as long axon growth during development and regeneration.
尽管成熟神经元中与发育性轴突生长相关的基因表达会急剧下降,但在正常和病理条件下,成体神经系统的轴突分支都会发生结构变化。此外,一些神经元在神经损伤后能支持长轴突的广泛再生。对培养的成体背根神经节(DRG)神经元的分析表明,不同类型轴突生长的能力取决于不同的基因表达模式。在没有持续转录的情况下,新分离的神经元在培养的第一天就能延伸出紧密、高度分支的树突。在接种前2 - 7天遭受外周轴突损伤的神经元支持一种独特的生长模式,其特征是长而稀疏分支的轴突快速延伸。幼稚的成体神经元在培养约24小时后会从“分支状”生长转变为“伸长状”生长,但在从完整动物身上取出神经节后,需要一段离散的新转录期。因此,外周轴突切断术(通过神经挤压或在切除DRG期间)会诱导一种依赖转录的变化,改变这些成体神经元能够执行的轴突生长类型。这种转变似乎在很大程度上是由逆行运输信号的中断触发的,因为在体内阻断轴突运输可以使许多DRG神经元获得伸长生长的能力。与外周轴突切断术相反,在体内中断DRG神经元的中枢投射轴突会导致随后在体外的生长,这种生长介于“分支状”和“伸长状”生长之间。这表明这两种生长模式之间的转变是一个多步骤过程,并且各个步骤可能受到单独调节。这些观察结果共同表明,成体神经系统中的结构重塑不一定涉及与发育和再生过程中长轴突生长相同的分子机制。