Mize R R
Department of Cell Biology and Anatomy, Louisiana State University Medical Center, 1901 Perdido Street, New Orleans, LA 70112, USA.
Brain Res. 1999 Oct 2;843(1-2):25-35. doi: 10.1016/s0006-8993(99)01847-8.
Recent evidence suggests that neurons containing the calcium binding proteins calbindin 28kD (CB) and parvalbumin (PV) have differing distributions which match respectively the distribution of W and Y retinal ganglion cell inputs to the cat superior colliculus (SC). In this study we have used electron microscope immunocytochemistry to study directly the synaptic inputs to neurons containing CB and PV. Aspiration lesions of areas 17-18 of visual cortex were made 4 days prior to sacrifice in order to identify degenerating cortical terminals (CT). Retinal terminals (RTs) were identified by their characteristic morphology including large round synaptic vesicles and pale mitochondria. We photographed RTs and CTs that were in contact with immunoreactive profiles sampled in both the superficial gray and optic layers (ol) of SC. CB immunoreactive (ir) dendrites were usually of small to medium caliber and were found to receive synaptic input from RTs. These RTs were all small profiles forming a single synaptic contact with asymmetric densifications. CBir profiles also received other synaptic input, including from terminals with dark mitochondria that contained flattened synaptic vesicles (F profiles). No CBir dendrites were found to receive CT input even though degenerating CTs were found in the vicinity of CBir profiles. By contrast, both RT and CT were found to contact PVir dendrites. RT terminals contacting PVir dendrites were both small and larger profiles with round synaptic vesicles and asymmetric synaptic densifications. CT were undergoing electron dense degeneration but still sometimes formed asymmetric synaptic densifications with PV neurons. PV cells also received F profile synaptic input. We conclude that CB neurons receive small RT synapses that are probably of W origin, while PV neurons receive both RT and CT synapses which are likely related to the Y pathway.
最近的证据表明,含有钙结合蛋白28kD钙结合蛋白(CB)和小白蛋白(PV)的神经元具有不同的分布,分别与猫上丘(SC)的W和Y视网膜神经节细胞输入的分布相匹配。在本研究中,我们使用电子显微镜免疫细胞化学直接研究对含有CB和PV的神经元的突触输入。在处死前4天对视觉皮层17-18区进行抽吸损伤,以识别退化的皮质终末(CT)。视网膜终末(RT)通过其特征性形态来识别,包括大的圆形突触小泡和浅色线粒体。我们拍摄了与在SC的浅灰色层和视层(ol)中采样的免疫反应性轮廓接触的RT和CT。CB免疫反应性(ir)树突通常为小到中等口径,发现它们接受来自RT的突触输入。这些RT都是小轮廓,与不对称致密化形成单个突触接触。CBir轮廓也接受其他突触输入,包括来自含有扁平突触小泡的深色线粒体终末(F轮廓)。即使在CBir轮廓附近发现了退化的CT,也没有发现CBir树突接受CT输入。相比之下,发现RT和CT都与PVir树突接触。与PVir树突接触的RT终末既有小的也有大的轮廓,具有圆形突触小泡和不对称突触致密化。CT正在经历电子致密性退变,但有时仍与PV神经元形成不对称突触致密化。PV细胞也接受F轮廓突触输入。我们得出结论,CB神经元接受可能起源于W的小RT突触,而PV神经元接受可能与Y通路相关的RT和CT突触。