Department of Anatomy & Neurobiology, School of Medicine, University of California, Irvine, California 92697, USA.
J Comp Neurol. 2012 Aug 1;520(11):2500-11. doi: 10.1002/cne.23050.
In primates, retinal inputs are relayed through the magno- and parvocells of the lateral geniculate nucleus (LGN) indirectly to extrastriate visual cortex. The most direct pathway identified to the extrastriate cortex is a disynaptic one that provides robust magno- and parvocellular inputs to the middle temporal area (MT). The inclusion of parvocells in this projection is somewhat surprising because of their importance for color and form vision, whereas MT is more strictly tuned to velocity. This raises the question of whether areas more involved in color and form processing, such as V4, receive similar projections. We report here on experiments that use rabies virus injections into V4 to retrogradely label mono- and disynaptic inputs. We find only a small number of labeled neurons in the LGN in a pattern consistent with monosynaptic labeling of koniocells, rather than disynaptic labeling of magno- and parvocells. The lack of robust magno- and parvocellular label was not due to ineffective viral transport because in the same cases we find hundreds of neurons labeled in the thalamic reticular nucleus, a structure that can only be labeled disynaptically from the cortex. We also find a complete absence of neurons labeled in V1, but thousands in adjacent areas V2 and V3. This result helps explain the absence of labeled magno- and parvocells in the LGN because disynaptic transport from an extrastriate visual area should require a relay through V1. Taken together, these results suggest that ascending magno/parvocellular inputs to V4 are more hierarchically organized than the relatively direct inputs to MT.
在灵长类动物中,视网膜输入通过外侧膝状体核(LGN)的大细胞和小细胞间接传递到视皮层。到视皮层的最直接途径是一种双突触途径,它为颞中区(MT)提供强大的大细胞和小细胞输入。这条投射通路包括小细胞有些令人惊讶,因为它们对颜色和形状视觉很重要,而 MT 则更严格地适应速度。这就提出了一个问题,即是否有更多涉及颜色和形状处理的区域,如 V4,接收类似的投射。我们在这里报告了使用狂犬病毒注射到 V4 来逆行标记单突触和双突触输入的实验。我们只在 LGN 中发现了少数标记神经元,其模式与 koniocells 的单突触标记一致,而不是大细胞和小细胞的双突触标记。缺乏强大的大细胞和小细胞标记并不是由于病毒运输无效,因为在相同的情况下,我们在丘脑网状核中发现了数百个神经元被标记,而丘脑网状核只能从皮层进行双突触标记。我们还发现 V1 中没有被标记的神经元,但在相邻的 V2 和 V3 区域有数千个被标记的神经元。这个结果有助于解释为什么在 LGN 中没有标记的大细胞和小细胞,因为来自视皮层的双突触投射应该需要通过 V1 进行中继。综上所述,这些结果表明,到 V4 的上升大/小细胞输入比到 MT 的相对直接输入在层次上更有组织。