Crockett D P, Harris S L, Egger M D
Department of Neuroscience and Cell Biology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854-5635, USA.
Anat Rec. 2000 Aug 1;259(4):446-60. doi: 10.1002/1097-0185(20000801)259:4<446::AID-AR80>3.0.CO;2-9.
We report on the transient, patterned expression of p75 in the ventrobasal (VB) thalamus, the major thalamic relay for somatosensation. We immunostained the brains of developing rats ranging in age from embryonic day (E) 14.5 to postnatal day (PD) 15 with an antibody against p75. To compare p75 expression with the developing synaptic organization within VB, we also immunolocalized the synaptic-vesicle-associated protein, synaptophysin (SYN), on alternate sections. p75-immunoreactivity (IR) was dense and uniform in the ventroposterior medial nucleus (VPM) in the late embryonic and early postnatal periods (E 16.5 to PD 3). In contrast, from PD 4-10, p75-IR in the VPM was patterned, reminiscent of cytochrome-oxidase-stained barreloids, a characteristic feature of the VB in rodents. By PD 14, p75-IR in the VPM was no longer detectable. The ventroposterior lateral nucleus (VPL), in contrast, exhibited no p75-IR. No p75-IR was detected in the ventroposterior lateral nucleus (VPL) at any developmental stage in which VPM could be distinguished from VPL. Light, but clearly patterned SYN-IR, first detectable on PD 2-3, increased in intensity in both VPL and VPM through PD 15. Sectioning the infraorbital nerve on PD 0 resulted in blurred patterns of p75- and SYN-IR within VPM in PD 7-9 rat pups. Removing large portions of the somatosensory cortex on PD 0 resulted in subsequent greatly reduced p75- and SYN-IR within VB. To specify the source of the p75-IR terminals, we stereotaxically injected into the VPM of PD 4-5 rats a monoclonal antibody to p75. One to 2 days later, IR of retrogradely transported p75 antibodies could be traced within axons and cell bodies of neurons associated with the trigeminothalamic pathway through the caudal diencephalon and mesencephalon; labelling was confined to the contralateral trigeminal principal sensory nucleus. The observed, transiently patterned p75-IR in VPM the early postpartum period suggests a role for p75 in synaptogenesis and pattern formation.
我们报告了p75在腹后基底(VB)丘脑(躯体感觉的主要丘脑中继站)中的短暂性、模式化表达。我们用抗p75抗体对年龄从胚胎期第(E)14.5天到出生后第(PD)15天的发育中大鼠的大脑进行免疫染色。为了比较p75表达与VB内发育中的突触组织,我们还在交替切片上对突触小泡相关蛋白突触素(SYN)进行了免疫定位。在胚胎后期和出生后早期(E 16.5至PD 3),腹后内侧核(VPM)中的p75免疫反应性(IR)密集且均匀。相比之下,从PD 4至10,VPM中的p75-IR呈模式化,让人联想到细胞色素氧化酶染色的桶状小体,这是啮齿动物VB的一个特征。到PD 14时,VPM中的p75-IR不再可检测到。相比之下,腹后外侧核(VPL)未表现出p75-IR。在任何能区分VPM和VPL的发育阶段,腹后外侧核(VPL)中均未检测到p75-IR。轻度但明显呈模式化的SYN-IR最早在PD 2至3时可检测到,在PD 15之前,其强度在VPL和VPM中均增加。在PD 0切断眶下神经,导致PD 7至9的幼鼠VPM内p75-IR和SYN-IR的模式模糊。在PD 0切除大部分躯体感觉皮层,导致随后VB内p75-IR和SYN-IR大大减少。为了确定p75-IR终末的来源,我们将抗p75单克隆抗体立体定向注射到PD 4至5大鼠的VPM中。1至2天后,可在与三叉丘脑通路相关的神经元的轴突和细胞体内追踪到逆行运输的p75抗体的IR,穿过尾侧间脑和中脑;标记仅限于对侧三叉神经主感觉核。在产后早期VPM中观察到的短暂性模式化p75-IR表明p75在突触发生和模式形成中起作用。