Payne B R, Lomber S G
Department of Anatomy and Neurobiology, Boston University School of Medicine, MA 02118, USA.
Exp Brain Res. 1998 Aug;121(3):334-49. doi: 10.1007/s002210050466.
We used anterograde and retrograde transsynaptic pathway tracing techniques to reveal the retinal origin and the cortical termination of the expanded retino-geniculo-middle suprasylvian (MS) cortex pathway in adult cats which sustained lesions of areas 17 and 18 on the day of birth (P1) or at 1 month of age (P28). Following anterograde transsynaptic transport of tritiated amino acids from the eye, four major results were obtained: (1) a strong and specific pathway from retina through dorsal lateral geniculate nucleus (dLGN) to the posterior half of MS cortex was identified; this pathway is a substantial expansion of an insignificant pathway present in intact cats; (2) the terminus of the pathway was lower layer III and layer IV; (3) contralateral projections were stronger than ipsilateral projections; (4) projections in P28 cats were stronger than those in P1 cats. Following retrograde transsynaptic transport of WGA-HRP from posterior MS cortex, four additional results were obtained: (1) the pathway was enlarged and visuotopically organized; (2) the pathway arose primarily from alpha- and gamma-retinal ganglion cells; (3) a small number of beta-cells in P1 cats and a modest number in P28 cats also contribute to the pathway; (4) the combined numbers of gamma- and beta-cells relative to alpha-cells was greater in temporal retina than in nasal retina. The combined demonstration of both origin and terminus of the pathway with transsynaptic tracers argued strongly for high levels of coupling between primary and secondary pathway limbs in both P1 and P28 cats. This level of coupling, as well as other features of the pathway, have much in common with the retino-geniculo-17/18 pathway of intact cats. However, the retino-geniculo-MS system in P1 cats transmits primarily Y and W signals, in P28 cats X, Y, and W signals; whereas the retino-geniculo-17/18 pathway transmits primarily X and Y signals. These results have implications for understanding the repercussions of early visual cortex lesions in monkeys and humans.
我们运用顺行和逆行跨突触通路示踪技术,来揭示成年猫中扩展的视网膜 - 膝状体 - 中颞上回(MS)皮质通路的视网膜起源和皮质终末,这些成年猫在出生当天(P1)或1月龄(P28)时遭受了17区和18区的损伤。在从眼睛进行氚标记氨基酸的顺行跨突触运输后,获得了四个主要结果:(1)确定了一条从视网膜经背外侧膝状核(dLGN)到MS皮质后半部的强大且特异的通路;这条通路是完整猫中一条无足轻重的通路的显著扩展;(2)该通路的终末位于第III层下部和第IV层;(3)对侧投射强于同侧投射;(4)P28猫中的投射强于P1猫中的投射。在从MS皮质后部进行WGA - HRP的逆行跨突触运输后,又获得了另外四个结果:(1)该通路扩大且具有视拓扑组织;(2)该通路主要起源于α和γ视网膜神经节细胞;(3)P1猫中的少量β细胞以及P28猫中的适量β细胞也对该通路有贡献;(4)相对于α细胞,γ和β细胞的总数在颞侧视网膜中比在鼻侧视网膜中更多。用跨突触示踪剂对该通路的起源和终末进行的联合展示有力地证明了P1和P28猫中初级和次级通路分支之间的高度耦合。这种耦合水平以及该通路的其他特征与完整猫的视网膜 - 膝状体 - 17/18通路有许多共同之处。然而,P1猫中的视网膜 - 膝状体 - MS系统主要传递Y和W信号,P28猫中传递X、Y和W信号;而视网膜 - 膝状体 - 17/18通路主要传递X和Y信号。这些结果对于理解猴子和人类早期视觉皮质损伤的影响具有启示意义。