Upton A L, Salichon N, Lebrand C, Ravary A, Blakely R, Seif I, Gaspar P
Institut National de la Santé et de la Recherche Médicale U106, Hôpital de la Salpêtrière, 75651 Paris cedex 13, France.
J Neurosci. 1999 Aug 15;19(16):7007-24. doi: 10.1523/JNEUROSCI.19-16-07007.1999.
Retinal ganglion cell (RGCs) project to the ipsilateral and contralateral sides of the brain in the dorsal lateral geniculate nucleus (dLGN) and the superior colliculus (SC). Projections from both eyes are initially intermingled until postnatal day 3 (P3) but segregate into eye-specific layers by P8. We report that this segregation does not occur in monoamine oxidase A knock-out mice (MAOA-KO) that have elevated brain levels of serotonin (5-HT) and noradrenaline. The abnormal development of retinal projections can be reversed by inhibiting 5-HT synthesis from P0 to P15. We found that in MAOA-KO mice, 5-HT accumulates in a subpopulation of RGCs and axons during embryonic and early postnatal development. The RGCs do not synthesize 5-HT but reuptake the amine from the extracellular space. In both MAOA-KO and normal mice, high-affinity uptake of 5-HT and serotonin transporter (SERT) immunoreactivity are observed in retinal axons from the optic cup to retinal terminal fields in the SC and dLGN. In the dLGN, transient SERT labeling corresponds predominantly to the ipsilateral retinal projection fields. We show that, in addition to SERT, developing RGCs also transiently express the vesicular monoamine transporter gene VMAT2: thus, retinal axons could store 5-HT in synaptic vesicles and possibly use it as a borrowed neurotransmitter. Finally we show that the 5-HT-1B receptor gene is expressed by RGCs throughout the retina from E15 until adult life. Activation of this receptor is known, from previous studies, to reduce retinotectal activity; thus 5-HT in excess could inhibit activity-dependent segregation mechanisms. A hypothesis is proposed whereby, during normal development, localized SERT expression could confer specific neurotransmission properties on a subset of RGCs and could be important in the fine-tuning of retinal projections.
视网膜神经节细胞(RGCs)投射至大脑同侧和对侧的背外侧膝状核(dLGN)和上丘(SC)。双眼的投射最初相互交织,直至出生后第3天(P3),但到P8时会分离成眼特异性层。我们报告称,在血清素(5-HT)和去甲肾上腺素脑水平升高的单胺氧化酶A基因敲除小鼠(MAOA-KO)中,这种分离不会发生。通过从P0到P15抑制5-HT合成,视网膜投射的异常发育可以得到逆转。我们发现,在MAOA-KO小鼠中,5-HT在胚胎期和出生后早期发育过程中在RGCs和轴突的一个亚群中积累。RGCs不合成5-HT,而是从细胞外空间重新摄取胺。在MAOA-KO小鼠和正常小鼠中,在从视杯到SC和dLGN中视网膜终末区域的视网膜轴突中都观察到5-HT的高亲和力摄取和血清素转运体(SERT)免疫反应性。在dLGN中,短暂的SERT标记主要对应于同侧视网膜投射区域。我们表明,除了SERT,发育中的RGCs还短暂表达囊泡单胺转运体基因VMAT2:因此,视网膜轴突可以将5-HT储存在突触小泡中,并可能将其用作借用的神经递质。最后我们表明,5-HT-1B受体基因在从E15到成年期的整个视网膜RGCs中表达。根据先前的研究,该受体的激活已知会降低视网膜顶盖活性;因此,过量的5-HT可能会抑制依赖活性的分离机制。提出了一个假说,即在正常发育过程中,局部SERT表达可以赋予一部分RGCs特定的神经传递特性,并且在视网膜投射的微调中可能很重要。