Department of Cell and Molecular Biology, Medical Faculty Mannheim, Heidelberg University, Ludolf-Krehl-Strasse 13-17, 68167 Mannheim, Germany; Nikon Imaging Center, Heidelberg University, Bioquant, 69120 Heidelberg, Germany; Cluster of Excellence CellNetworks, Heidelberg University, Bioquant, 69120 Heidelberg, Germany.
Nikon Imaging Center, Heidelberg University, Bioquant, 69120 Heidelberg, Germany; Cluster of Excellence CellNetworks, Heidelberg University, Bioquant, 69120 Heidelberg, Germany.
Curr Biol. 2017 Jan 23;27(2):270-278. doi: 10.1016/j.cub.2016.11.038. Epub 2017 Jan 5.
Most neuronal populations form on both the left and right sides of the brain. Their efferent axons appear to grow synchronously along similar pathways on each side, although the neurons or their environment often differ between the two hemispheres [1-4]. How this coordination is controlled has received little attention. Frequently, neurons establish interhemispheric connections, which can function to integrate information between brain hemispheres (e.g., [5]). Such commissures form very early, suggesting their potential developmental role in coordinating ipsilateral axon navigation during embryonic development [4]. To address the temporal-spatial control of bilateral axon growth, we applied long-term time-lapse imaging to visualize the formation of the conserved left-right asymmetric habenular neural circuit in the developing zebrafish embryo [6]. Although habenular neurons are born at different times across brain hemispheres [7], we found that elongation of habenular axons occurs synchronously. The initiation of axon extension is not controlled within the habenular network itself but through an early developing proximal diencephalic network. The commissural neurons of this network influence habenular axons both ipsilaterally and contralaterally. Their unilateral absence impairs commissure formation and coordinated habenular axon elongation and causes their subsequent arrest on both sides of the brain. Thus, habenular neural circuit formation depends on a second intersecting commissural network, which facilitates the exchange of information between hemispheres required for ipsilaterally projecting habenular axons. This mechanism of network formation may well apply to other circuits, and has only remained undiscovered due to technical limitations.
大多数神经元群体在大脑的左右两侧形成。它们的传出轴突似乎沿着每一侧的相似路径同步生长,尽管神经元或其环境在两个半球之间经常不同[1-4]。这种协调是如何控制的还没有得到太多关注。通常,神经元会建立半球间的连接,这些连接可以起到整合大脑半球之间信息的作用(例如,[5])。这种连合很早就形成了,这表明它们在胚胎发育过程中协调同侧轴突导航方面具有潜在的发育作用[4]。为了研究双侧轴突生长的时空控制,我们应用长期延时成像技术来可视化发育中的斑马鱼胚胎中保守的左右不对称缰状核神经回路的形成[6]。尽管缰状核神经元在大脑半球的不同时间出生[7],但我们发现缰状核轴突的伸长是同步的。轴突延伸的启动不是由缰状核网络本身控制的,而是通过早期发育的近端间脑网络控制的。该网络的连合神经元对同侧和对侧的缰状核轴突都有影响。它们单侧缺失会损害连合形成和协调的缰状核轴突伸长,并导致它们随后在大脑两侧的阻滞。因此,缰状核神经回路的形成取决于第二个交叉连合网络,该网络促进了同侧投射缰状核轴突之间所需的信息交换。这种网络形成的机制可能适用于其他回路,只是由于技术限制,一直没有被发现。