Kumaratilake J S, Gibson M A, Fanning J C, Cleary E G
Department of Pathology, University of Adelaide, South Australia.
Eur J Cell Biol. 1989 Oct;50(1):117-27.
Elastic tissue, when viewed in the electron microscope, consists of an amorphous component that is immunoreactive with anti-tropoelastin (TE) antibodies and microfibrils, that react with monospecific antibodies against a 31 kDa microfibrillar glycoprotein constituent, called MAGP. A detailed study of the tissue distribution of microfibrils and of the two elastic tissue antibodies has been carried out, using single and double-labeled immunogold techniques in high resolution electron microscopy. Microfibrils similar in appearance to those associated with elastic tissue and immunoreactive with the anti-MAGP antibody, have been demonstrated in many tissues in the absence of amorphous elastic tissue. In the majority of these tissues, specific anti-TE antibody localization was demonstrated in the immediate vicinity of the microfibrils, or alternatively, the microfibrils were shown to be in direct continuity with microfibrils of similar morphology, which were associated with material immunoreactive with anti-TE antibody. The diameter of these microfibrils varied between 8 nm and 16 nm. They were unbranched structures of indefinite length, with a tubular profile on cross section and periodic staining in longitudinal section. In some tissues, notably in the ciliary zonule and in the mesangial region of the renal glomerulus, microfibrils of similar morphology were demonstrated which were immunoreactive with anti-MAGP antibody, but which were unrelated to amorphous elastic tissue and with which anti-TE antibody localization could not be demonstrated. The evidence available supports the conclusion that all these microfibrils are members of a single class of structures, which are widely distributed in the tissues and which are secreted by a range of cell types. Attention is directed to the close relationship between these microfibrils and the basement membrane of the glomerulus, of uterine smooth muscle, of the basal cells of the epidermis and of the reticulum cells of the spleen.
在电子显微镜下观察时,弹性组织由一种与抗原弹性蛋白(TE)抗体发生免疫反应的无定形成分和微原纤维组成,微原纤维与针对一种名为MAGP的31 kDa微原纤维糖蛋白成分的单特异性抗体发生反应。利用高分辨率电子显微镜中的单标记和双标记免疫金技术,对微原纤维和两种弹性组织抗体的组织分布进行了详细研究。在许多没有无定形弹性组织的组织中,已证实存在外观与弹性组织相关且与抗MAGP抗体发生免疫反应的微原纤维。在这些组织中的大多数中,特异性抗TE抗体定位于微原纤维的紧邻区域,或者,微原纤维被证明与形态相似的微原纤维直接连续,这些微原纤维与抗TE抗体免疫反应性物质相关。这些微原纤维的直径在8纳米至16纳米之间变化。它们是长度不定的无分支结构,横截面呈管状,纵截面有周期性染色。在一些组织中,特别是在睫状小带和肾小球系膜区,已证实存在形态相似的微原纤维,它们与抗MAGP抗体发生免疫反应,但与无定形弹性组织无关,且无法证明抗TE抗体的定位。现有证据支持这样的结论:所有这些微原纤维都是一类单一结构的成员,它们广泛分布于组织中,并由一系列细胞类型分泌。需要注意的是这些微原纤维与肾小球、子宫平滑肌、表皮基底细胞和脾网状细胞的基底膜之间的密切关系。