Fried K, Nosrat C, Lillesaar C, Hildebrand C
Department of Neuroscience, Karolinska Institute, Stockholm, Sweden.
Crit Rev Oral Biol Med. 2000;11(3):318-32. doi: 10.1177/10454411000110030301.
The purpose of this review is to discuss molecular factors influencing nerve growth to teeth. The establishment of a sensory pulpal innervation occurs concurrently with tooth development. Epithelial/mesenchymal interactions initiate the tooth primordium and change it into a complex organ. The initial events seem to be controlled by the epithelium, and subsequently, the mesenchyme acquires odontogenic properties. As yet, no single initiating epithelial or mesenchymal factor has been identified. Axons reach the jaws before tooth formation and form terminals near odontogenic sites. In some species, local axons have an initiating function in odontogenesis, but it is not known if this is also the case with mammals. In diphyodont mammals, the primary dentition is replaced by a permanent dentition, which involves a profound remodeling of terminal pulpal axons. The molecular signals underlying this remodeling remain unknown. Due to the senescent deterioration of the dentition, the target area of tooth nerves shrinks with age, and these nerves show marked pathological-like changes. Nerve growth factor and possibly also brain-derived neurotrophic factor seem to be important in the formation of a sensory pulpal innervation. Neurotrophin-3 and -4/5 are probably not involved. In addition, glial cell line-derived neurotrophic factor, but not neurturin, seems to be involved in the control of pulpal axon growth. A variety of other growth factors may also influence developing tooth nerves. Many major extracellular matrix molecules, which can influence growing axons, are present in developing teeth. It is likely that these molecules influence the growing pulpal axons.
本综述的目的是讨论影响神经向牙齿生长的分子因素。感觉牙髓神经支配的建立与牙齿发育同时发生。上皮/间充质相互作用启动牙原基并将其转变为一个复杂的器官。最初的事件似乎由上皮控制,随后间充质获得成牙特性。然而,尚未确定单一的起始上皮或间充质因子。轴突在牙齿形成之前到达颌骨并在成牙部位附近形成终末。在一些物种中,局部轴突在牙发生中具有起始功能,但尚不清楚哺乳动物是否也是如此。在双牙列哺乳动物中,乳牙列被恒牙列取代,这涉及牙髓终末轴突的深刻重塑。这种重塑背后的分子信号仍然未知。由于牙列的衰老退化,牙齿神经的靶区域随年龄缩小,并且这些神经表现出明显的病理样变化。神经生长因子以及可能还有脑源性神经营养因子似乎在感觉牙髓神经支配的形成中很重要。神经营养蛋白-3和-4/5可能不参与其中。此外,胶质细胞系衍生的神经营养因子而非神经营养素似乎参与牙髓轴突生长的控制。多种其他生长因子也可能影响发育中的牙齿神经。许多可影响轴突生长的主要细胞外基质分子存在于发育中的牙齿中。这些分子很可能影响生长中的牙髓轴突。