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猪外周神经沃勒变性中膜肽酶的细胞重组

Cellular reorganisation of membrane peptidases in Wallerian degeneration of pig peripheral nerve.

作者信息

Kenny A J, Bourne A

机构信息

Department of Biochemistry & Molecular Biology, University of Leeds, UK.

出版信息

J Neurocytol. 1991 Nov;20(11):875-85. doi: 10.1007/BF01190466.

Abstract

Immunohistochemical techniques have been used to study a group of membrane peptidases in the distal segment of the ulnar nerve of piglets 7 and 14 days after surgical section. Five peptidases were studied, all of which have a wide distribution on the surfaces of many cell types and have roles in metabolising neuropeptides. In normal pig nerves, endopeptidase-24.11 is expressed by both myelin- and nonmyelin-forming Schwann cells. Peptidyl dipeptidase A (angiotensin converting enzyme), aminopeptidase-N and dipeptidyl peptidase IV are present in the microvessels, and aminopeptidase-N is also seen in the perineurial connective tissue. Of this group of peptidases, only aminopeptidase-W is a neuronal marker in normal nerve. Macrophages were identified by two antibodies, 74-22-15 and 40D (which recognises Ia). Short-term cultures of macrophages obtained by alveolar lavage were positively stained by both antibodies and about half of the cells also expressed aminopeptidase-N and dipeptidyl peptidase IV. Staining by 40D and 74-22-15 revealed the presence of significant numbers of macrophages in normal nerve, but none of the membrane peptidases colocalized with these cells. Seven days after section of the nerve, the distal segment showed morphological changes typical of Wallerian degeneration. Endopeptidase-24.11 was no longer visible in myelin sheaths, but remained a marker for the surface of Schwann cells (defined also by staining for glial fibrillary acidic protein). The macrophage markers revealed marked changes in the morphology of these cells, often consistent with their phagocytic activity. Two peptidases, aminopeptidase-N and aminopeptidase-W, also appeared at this time to be associated with cells exhibiting the morphology of activated macrophages. This association could be confirmed in many instances by double staining with 74-22-15 and antibodies to the peptidases. Angiotensin converting enzyme retained its single location in microvessels at 7 days after section, but at 14 days a new pattern emerged as it, too, was expressed by macrophages. Dipeptidyl peptidase IV was not shown to be a macrophage marker in the degenerating nerve. Thus Wallerian degeneration leads to remarkable changes in the cellular expression of membrane peptidase; endopeptidase-24.11 reflects the changed morphology of Schwann cells while aminopeptidase-N, aminopeptidase-W and angiotensin converting enzyme become expressed by the actively phagocytosing macrophages.

摘要

免疫组织化学技术已被用于研究仔猪尺神经手术切断后7天和14天远段的一组膜肽酶。研究了五种肽酶,它们在许多细胞类型的表面广泛分布,并且在神经肽代谢中起作用。在正常猪神经中,髓鞘形成和非髓鞘形成的施万细胞均表达内肽酶-24.11。肽基二肽酶A(血管紧张素转换酶)、氨肽酶-N和二肽基肽酶IV存在于微血管中,氨肽酶-N也见于神经束膜结缔组织中。在这组肽酶中,只有氨肽酶-W是正常神经中的神经元标志物。用两种抗体74-22-15和40D(识别Ia)鉴定巨噬细胞。通过肺泡灌洗获得的巨噬细胞短期培养物被两种抗体阳性染色,约一半的细胞还表达氨肽酶-N和二肽基肽酶IV。40D和74-22-15染色显示正常神经中存在大量巨噬细胞,但没有一种膜肽酶与这些细胞共定位。神经切断7天后,远段出现典型的瓦勒变性形态学变化。髓鞘中不再可见内肽酶-24.11,但它仍然是施万细胞表面的标志物(也通过胶质纤维酸性蛋白染色来界定)。巨噬细胞标志物显示这些细胞的形态有明显变化,这通常与其吞噬活性一致。此时,两种肽酶,氨肽酶-N和氨肽酶-W,也似乎与表现出活化巨噬细胞形态的细胞相关。在许多情况下,用74-22-15和肽酶抗体双重染色可以证实这种关联。血管紧张素转换酶在切断后7天仍保留在微血管中的单一位置,但在14天时出现了一种新模式,因为它也由巨噬细胞表达。在变性神经中,二肽基肽酶IV未显示为巨噬细胞标志物。因此,瓦勒变性导致膜肽酶的细胞表达发生显著变化;内肽酶-24.11反映了施万细胞形态的改变,而氨肽酶-N、氨肽酶-W和血管紧张素转换酶则由活跃吞噬的巨噬细胞表达。

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