Blumer Roland, Konakci Kadriye Zeynep, Pomikal Christine, Wieczorek Grazyna, Lukas Julius-Robert, Streicher Johannes
Center of Anatomy and Cell Biology, Medical University Vienna, Vienna, Austria.
Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1176-86. doi: 10.1167/iovs.08-2748. Epub 2008 Oct 20.
This study aims to complement the authors' prior findings on palisade endings in extraocular muscles (EOMs) of monkeys, and to clarify whether palisade endings are cholinergic motor or cholinergic sensory.
Macaque monkeys (Macaca fascicularis, n = 10) of both sexes were analyzed using three-dimensional (3D) reconstructions, confocal laser scanning microscopy (CLSM), and conventional/immuno transmission electron microscopy (TEM). For CLSM, we used three combinations of triple fluorescent labeling. EOM wholemounts were labeled with cholinergic markers, including choline acetyltransferase (ChAT), choline transporter (ChT), vesicular acetylcholine transporter (VAChT), and a classical postsynaptic marker for motor terminals, namely alpha-bungarotoxin. Muscle fibers were counterstained with phalloidin. 3D reconstructions were done of triple-labeled palisade endings. For immuno TEM, tissue was labeled with antibody against ChAT.
Concordant with prior findings, the authors demonstrated that palisade endings at the muscle fiber tips arose from nerve fibers that are ChAT-positive. In 25% of the cases, axons forming palisade endings established multiple neuromuscular contacts outside the palisade complex. Such additional neuromuscular contacts were motor terminals, as demonstrated by alpha-bungarotoxin binding. All palisade endings established nerve terminals on the tendon. In 40% of the palisade endings, nerve terminals were observed on the muscle fiber as well. Neurotendinous contacts and neuromuscular contacts in palisade endings were ChT/ChAT/VAChT-immunoreactive. Neuromuscular contacts exhibited structural features of motor terminals and were also alpha-bungarotoxin positive.
The present study ascertained that palisade endings are cholinergic motor organs. Therefore, it was concluded that palisade endings are not candidates to provide eye-position signals.
本研究旨在补充作者先前关于猴子眼外肌(EOMs)栅栏状末梢的研究结果,并阐明栅栏状末梢是胆碱能运动性的还是胆碱能感觉性的。
使用三维(3D)重建、共聚焦激光扫描显微镜(CLSM)以及传统/免疫透射电子显微镜(TEM)对10只成年猕猴(食蟹猴)进行分析。对于CLSM,我们使用了三种三重荧光标记组合。EOM整装标本用胆碱能标记物进行标记,包括胆碱乙酰转移酶(ChAT)、胆碱转运体(ChT)、囊泡乙酰胆碱转运体(VAChT),以及用于运动终末的经典突触后标记物,即α-银环蛇毒素。肌纤维用鬼笔环肽进行复染。对三重标记的栅栏状末梢进行3D重建。对于免疫TEM,组织用抗ChAT抗体进行标记。
与先前的研究结果一致,作者证明肌纤维末端的栅栏状末梢起源于ChAT阳性的神经纤维。在25%的病例中,形成栅栏状末梢的轴突在栅栏复合体之外建立了多个神经肌肉接触。如α-银环蛇毒素结合所示,这种额外的神经肌肉接触是运动终末。所有栅栏状末梢都在肌腱上建立了神经末梢。在40%的栅栏状末梢中,也观察到了在肌纤维上的神经末梢。栅栏状末梢中的神经腱接触和神经肌肉接触均为ChT/ChAT/VAChT免疫反应性。神经肌肉接触表现出运动终末结构特征,且α-银环蛇毒素呈阳性。
本研究确定栅栏状末梢是胆碱能运动器官。因此,得出结论,栅栏状末梢不是提供眼位信号的候选者。