Zhang X, Bean A J, Wiesenfeld-Hallin Z, Hökfelt T
Department of Neuroscience, Karolinska Institute, Stockholm, Sweden.
Neuroscience. 1995 Feb;64(4):917-41. doi: 10.1016/0306-4522(94)00487-p.
Using immunofluorescence histochemistry and pre- and post-embedding immunoelectron microscopy the rat lumbar dorsal horn was analysed in normal rats and 14 days after unilateral transection of the sciatic nerve. A marked increase in neuropeptide Y-like immunoreactivity was observed in the ipsilateral, superficial dorsal horn, especially in laminae III and IV, of the lumbar 4-5 spinal cord segments after peripheral axotomy. In the ipsilateral lamina II two types of neuropeptide Y-immunoreactive, presumably primary afferent terminals could be identified at the ultrastructural level. The first type contained many large dense-core vesicles (100-155 nm in diameter), whereas a second, more common type had only a few and smaller large dense-core vesicles (80-100 nm in diameter), plus synaptic vesicles of varying diameter (50-85 nm), large empty vesicles and tubular structures. Only occasionally were neuropeptide Y-positive terminals in lamina II involved in the formation of axonal labyrinths. In the ipsilateral lamina III, the number of neuropeptide Y-positive nerve terminals markedly increased after axotomy, with a moderate increase in lamina IV. These neuropeptide Y-positive terminals were morphologically similar to the second type of neuropeptide Y-positive terminal in lamina II, i.e. contained many synaptic vesicles (45-50 nm in diameter), a few small large dense-core vesicles (80-100 nm in diameter), electron-dense granular matrix and a few tubular structures. Fusion of synaptic vesicles with the plasma membrane was often observed at these synapses. These terminals frequently formed glomeruli but were not involved in axonal labyrinths. With regard to local neurons, neuropeptide Y-like immunoreactivity was observed in many dendrite-like profiles mostly making synaptic contacts with neuropeptide Y-negative dendrites and only rarely contacting the central terminal of the glomeruli. Neuropeptide Y-positive nerve endings were mainly seen in lamina I and the outer third of lamina II. After peripheral axotomy the number of vasoactive intestinal polypeptide/peptide histidine isoleucine immunoreactive terminals was increased in laminae I and II. They contained many large dense-core vesicles (100-120 nm in diameter), and some of them were positive for vasoactive intestinal polypeptide/peptide histidine isoleucine. Morphologically, the terminals were characterized by a granular matrix, tubular structures, empty vesicles, reduction in synaptic vesicles and absence of postsynaptic densities. Vasoactive intestinal polypeptide/peptide histidine isoleucine-like immunoreactivities were often found in association with labyrinth formation.(ABSTRACT TRUNCATED AT 400 WORDS)
采用免疫荧光组织化学以及包埋前和包埋后免疫电子显微镜技术,对正常大鼠以及坐骨神经单侧横断术后14天大鼠的腰段背角进行分析。在外周轴突切断后,在腰4 - 5脊髓节段同侧浅表背角,尤其是III层和IV层,观察到神经肽Y样免疫反应性显著增加。在同侧II层,在超微结构水平可识别出两种神经肽Y免疫反应性的、推测为初级传入终末。第一种类型含有许多大的致密核心囊泡(直径100 - 155 nm),而第二种更常见的类型只有少数且较小的大致密核心囊泡(直径80 - 100 nm),加上不同直径(50 - 85 nm)的突触囊泡、大的空泡和管状结构。II层中神经肽Y阳性终末仅偶尔参与轴突迷路的形成。在同侧III层,轴突切断后神经肽Y阳性神经终末数量显著增加,IV层有中度增加。这些神经肽Y阳性终末在形态上与II层中第二种类型的神经肽Y阳性终末相似,即含有许多突触囊泡(直径45 - 50 nm)、少数小的大致密核心囊泡(直径80 - 100 nm)、电子致密颗粒基质和一些管状结构。在这些突触处经常观察到突触囊泡与质膜融合。这些终末经常形成小球,但不参与轴突迷路。关于局部神经元,在许多树突样结构中观察到神经肽Y样免疫反应性,这些结构大多与神经肽Y阴性树突形成突触联系,仅偶尔与小球的中央终末接触。神经肽Y阳性神经末梢主要见于I层和II层外侧三分之一。外周轴突切断后,I层和II层中血管活性肠肽/肽组氨酸异亮氨酸免疫反应性终末数量增加。它们含有许多大的致密核心囊泡(直径100 - 120 nm),其中一些对血管活性肠肽/肽组氨酸异亮氨酸呈阳性。在形态上,这些终末的特征是颗粒基质、管状结构、空泡、突触囊泡减少以及无突触后致密物。血管活性肠肽/肽组氨酸异亮氨酸样免疫反应性常与迷路形成相关。(摘要截短于400字)