Department of Neuroscience, University of Wisconsin School of Medicine and Public Health, Madison, WI 53705, USA.
J Comp Neurol. 2012 Jan 1;520(1):34-51. doi: 10.1002/cne.22682.
The ventral and dorsal medial geniculate (MGV and MGD) constitute the major auditory thalamic subdivisions providing thalamocortical inputs to layer IV and lower layer III of auditory cortex. No quantitative evaluation of this projection is available. Using biotinylated dextran amine (BDA)/biocytin injections, we describe the cortical projection patterns of MGV and MGD cells. In primary auditory cortex the bulk of MGV axon terminals are in layer IV/lower layer III with minor projections to supragranular layers and intermediate levels in infragranular layers. MGD axons project to cortical regions designated posterodorsal (PD) and ventral (VA) showing laminar terminal distributions that are quantitatively similar to the MGV-to-primary cortex terminal distribution. At the electron microscopic level MGV and MGD terminals are non-γ-aminobutyric acid (GABA)ergic with MGD terminals in PD and VA slightly but significantly larger than MGV terminals in primary cortex. MGV/MGD terminals synapse primarily onto non-GABAergic spines/dendrites. A small number synapse on GABAergic structures, contacting large dendrites or cell bodies primarily in the major thalamocortical recipient layers. For MGV projections to primary cortex or MGD projections to PD or VA, the non-GABAergic postsynaptic structures at each site were the same size regardless of whether they were in supragranular, granular, or infragranular layers. However, the population of MGD terminal-recipient structures in VA were significantly larger than the MGD terminal-recipient structures in PD or the MGV terminal-recipient structures in primary cortex. Thus, if terminal and postsynaptic structure size indicate strength of excitation then MGD to VA inputs are strongest, MGD to PD intermediate, and MGV to primary cortex the weakest.
腹侧和背侧内侧膝状体(MGV 和 MGD)构成了主要的听觉丘脑亚区,为听觉皮层的 IV 层和 III 层下部提供丘脑皮质输入。目前尚无对此投射进行定量评估的方法。我们使用生物素化葡聚糖胺(BDA)/生物胞素注射,描述了 MGV 和 MGD 细胞的皮质投射模式。在初级听觉皮层中,MGV 轴突末梢的大部分位于 IV 层/III 层下部,少量投射到颗粒上层和颗粒下层中间层。MGD 轴突投射到后背侧(PD)和腹侧(VA)指定的皮质区域,表现出与 MGV 到初级皮层末端分布相似的层状末端分布。在电子显微镜水平,MGV 和 MGD 末端是非γ-氨基丁酸(GABA)能的,PD 和 VA 中的 MGD 末端略大于初级皮层中的 MGV 末端。MGV/MGD 末端主要与非 GABA 能棘突/树突形成突触。少数与 GABA 能结构形成突触,主要与主要的丘脑皮质接受层中的大树突或细胞体接触。对于 MGV 到初级皮层的投射或 MGD 到 PD 或 VA 的投射,每个部位的非 GABA 能突触后结构的大小相同,无论它们位于颗粒上层、颗粒层还是颗粒下层。然而,VA 中 MGD 末端接受结构的群体明显大于 PD 中 MGD 末端接受结构或初级皮层中 MGV 末端接受结构。因此,如果末端和突触后结构的大小表示兴奋的强度,那么 MGD 到 VA 的输入最强,MGD 到 PD 的输入次之,MGV 到初级皮层的输入最弱。