ten Donkelaar H J
Department of Neurology, University Hospital Nijmegen, The Netherlands.
Adv Anat Embryol Cell Biol. 2000;154:iii-ix, 1-145. doi: 10.1007/978-3-642-57125-1.
Throughout tetrapods a basic pattern in the organization of descending supraspinal pathways is present. The most notable difference between nonmammalian tetrapods and mammals is the apparent absence of somatomotor cortical areas giving rise to long descending projections to the spinal cord. The phylogenetic constancy of descending supraspinal pathways, at least of those arising in the brain stem, probably implies a comparable pattern of development, presumably a developmental sequence in the formation of these central motor pathways. For studies on the development of motor systems, anurans such as the clawed toad, Xenopus laevis, chicken embryos, and opossums are very attractive animals. Moreover, in these species as well as in rodents in vitro approaches can be used. In the present survey, current knowledge on the neurogenesis, axonal outgrowth, synaptogenesis, and developmental plasticity of the central motor pathways in tetrapods including the sparse data available for man, is discussed. These data are placed in the perspective of the development of the spinal cord and, where possible, correlated with functional data. Emphasis is on the clawed toad, X. laevis, chicken embryos, and opossum and rodent data. The outgrowth of axons of descending supraspinal pathways can be regarded as the result of a series of distinct processes, which may be expressed in a coordinated program: (1) the outgrowth of axons and selection of pathways to their appropriate destination; (2) dendritic outgrowth and formation of specific dendritic morphology; (3) selection of specific targets and collateralization by axons; (4) elimination of incorrect and redundant synapses, axonal and dendritic branches, and of mismatched neurons; and (5) functional refinement of synaptic connections. Tracer and transmitter immunohistochemistry in Xenopus laevis showed that from the moment cell division stops, an axon is formed followed by dendrites which emerge from the cell body. At the beginning of the cell differentiation phase the production of the cell-specific neuroactive substances takes place. Initial outgrowth is in a specific direction for each class of neuron. It is likely that all descending supraspinal pathways arise in a similar way. In the spinal projections of each of the descending supraspinal pathways three stages can be distinguished: (1) an initial stage of outgrowth to the spinal cord, (2) a short "waiting" period after which collaterals enter the spinal gray matter, and (3) myelination of axons. An "overshoot" of spinal projections is particularly evident for the mammalian corticospinal tract. The pattern of early descending axonal tracts appears to be similar in all vertebrate groups. Early axons lay down an axonal scaffold containing guidance cues that are available to later generated growth cones. Throughout vertebrates including man, the fasciculus longitudinalis medialis (flm) is the first descending pathway to be formed. Interstitiospinal fibers "pioneer" this tract, and are joined by reticulospinal fibers. Vestibulospinal fibers (the medial vestibulospinal tract) follow much later. The lateral vestibulospinal tract takes a separate course through the brain stem. Late-arriving fiber tracts such as the rubrospinal and corticospinal tracts probably have their own mechanism of selecting the appropriate pathway. The formation of the descending supraspinal pathways occurs according to a developmental sequence. In all tetrapods studied, reticulospinal and interstitiospinal fibers reach the spinal cord first, followed by vestibulospinal fibers and, much later, by rubrospinal and, if present, corticospinal projections. A special case is presented by anurans which in fact have two motor systems, a primary, transient motor system and a secondary, definitive motor system. Reticulospinal, interstitiospinal and vestibulospinal fibers innervate the spinal cord very early in development, well before the development of the hindlimbs. Rubrospinal fibers in
在所有四足动物中,存在一种下行脊髓上通路组织的基本模式。非哺乳类四足动物与哺乳动物之间最显著的区别在于,明显不存在向脊髓发出长下行投射的躯体运动皮层区域。下行脊髓上通路的系统发育恒定性,至少是那些起源于脑干的通路,可能意味着一种类似的发育模式,大概是这些中枢运动通路形成过程中的一个发育序列。对于运动系统发育的研究而言,诸如爪蟾、非洲爪蟾、鸡胚胎和负鼠等无尾两栖类动物是非常有吸引力的研究对象。此外,在这些物种以及啮齿动物中,可以采用体外研究方法。在本综述中,讨论了关于四足动物中枢运动通路的神经发生、轴突生长、突触形成和发育可塑性的当前知识,包括人类的稀少数据。这些数据从脊髓发育的角度进行考量,并在可能的情况下与功能数据相关联。重点在于爪蟾、非洲爪蟾、鸡胚胎以及负鼠和啮齿动物的数据。下行脊髓上通路轴突的生长可被视为一系列不同过程的结果,这些过程可能在一个协调的程序中得以体现:(1)轴突生长以及选择通向其合适目的地的路径;(2)树突生长以及特定树突形态的形成;(3)轴突对特定靶标的选择以及分支形成;(4)消除不正确和多余的突触、轴突和树突分支以及不匹配的神经元;(5)突触连接的功能精细化。对非洲爪蟾进行的示踪剂和递质免疫组织化学研究表明,从细胞分裂停止的那一刻起,轴突开始形成,随后树突从细胞体中伸出。在细胞分化阶段开始时,细胞特异性神经活性物质开始产生。每一类神经元的初始生长都朝着特定方向进行。很可能所有下行脊髓上通路都是以类似的方式产生的。在每条下行脊髓上通路的脊髓投射中,可以区分出三个阶段:(1)向脊髓生长的初始阶段;(2)一个短暂的“等待”期,之后分支进入脊髓灰质;(3)轴突的髓鞘形成。哺乳动物皮质脊髓束的脊髓投射“过度生长”现象尤为明显。早期下行轴突束的模式在所有脊椎动物类群中似乎都很相似。早期轴突形成一个包含引导线索的轴突支架,可供后来生成的生长锥利用。在包括人类在内的所有脊椎动物中,内侧纵束(flm)是最早形成的下行通路。间质脊髓纤维“开拓”了这条通路,并与网状脊髓纤维相连。前庭脊髓纤维(内侧前庭脊髓束)则要晚得多才出现。外侧前庭脊髓束在脑干中走行独立。诸如红核脊髓束和皮质脊髓束等较晚到达的纤维束可能有其自身选择合适路径的机制。下行脊髓上通路的形成按照一个发育序列进行。在所有研究的四足动物中,网状脊髓纤维和间质脊髓纤维首先到达脊髓,随后是前庭脊髓纤维,再晚得多才是红核脊髓纤维,如果存在的话,还有皮质脊髓投射。无尾两栖类动物呈现出一种特殊情况,实际上它们有两个运动系统,一个主要的、短暂的运动系统和一个次要的、确定的运动系统。网状脊髓纤维、间质脊髓纤维和前庭脊髓纤维在发育早期就支配脊髓,远早于后肢的发育。红核脊髓纤维在……