Bruns R R, Press W, Engvall E, Timpl R, Gross J
J Cell Biol. 1986 Aug;103(2):393-404. doi: 10.1083/jcb.103.2.393.
Filaments and fibrils that exhibit a 100-nm axial periodicity and occur in the medium and in the deposited extracellular matrix of chicken embryo and human fibroblast cultures have been tentatively identified with type VI collagen on the basis of their similar structural characteristics (Bruns, R. R., 1984, J. Ultrastruct. Res., 89:136-145). Using indirect immunoelectron microscopy and specific monoclonal and polyclonal antibodies, we now report their positive identification with collagen VI and their distribution in fibroblast cultures and in tendon. Primary human foreskin fibroblast cultures, labeled with anti-type VI antibody and studied by fluorescence microscopy, showed a progressive increase in labeling and changes in distribution with time up to 8 d in culture. With immunoelectron microscopy and monoclonal antibodies to human type VI collagen followed by goat anti-mouse IgG coupled to colloidal gold, they showed in thin sections specific 100-nm periodic labeling on extracellular filaments and fibrils: one monoclonal antibody (3C4) attached to the band region and another (4B10) to the interband region of the filaments and fibrils. Rabbit antiserum to type VI collagen also localized on the band region, but the staining was less well defined. Control experiments with antibodies to fibronectin and to procollagen types I and III labeled other filaments and fibrils, but not those with a 100-nm period. Heavy metal-stained fibrils with the same periodic and structural characteristics also have been found in both adult rat tail tendon and embryonic chicken tendon subjected to prolonged incubation in culture medium or treatment with adenosine 5'-triphosphate at pH 4.6. We conclude that the 100-nm periodic filaments and fibrils represent the native aggregate form of type VI collagen. It is likely that banded fibrils of the same periodicity and appearance, reported by many observers over the years in a wide range of normal and pathological tissues, are at least in part, type VI collagen.
基于其相似的结构特征,已初步将在鸡胚和人成纤维细胞培养物的培养基及沉积的细胞外基质中出现的、具有100纳米轴向周期性的细丝和原纤维鉴定为VI型胶原(布伦斯,R. R.,1984年,《超微结构研究杂志》,89卷:136 - 145页)。使用间接免疫电子显微镜以及特异性单克隆和多克隆抗体,我们现在报告它们被确认为VI型胶原,并阐述它们在成纤维细胞培养物和肌腱中的分布情况。用抗VI型抗体标记的原代人包皮成纤维细胞培养物,通过荧光显微镜观察,结果显示随着培养时间长达8天,标记逐渐增加且分布发生变化。通过免疫电子显微镜以及针对人VI型胶原的单克隆抗体,随后用与胶体金偶联的山羊抗小鼠IgG进行检测,在薄切片中它们显示出细胞外细丝和原纤维上有特异性的100纳米周期性标记:一种单克隆抗体(3C4)附着于细丝和原纤维的条带区域,另一种(4B10)附着于带间区域。抗VI型胶原的兔抗血清也定位于条带区域,但染色不太清晰。用抗纤连蛋白以及I型和III型前胶原抗体进行的对照实验标记了其他细丝和原纤维,但未标记具有100纳米周期的那些。在成年大鼠尾腱和胚胎鸡腱中,经过在培养基中长时间孵育或在pH 4.6条件下用5'-三磷酸腺苷处理后,也发现了具有相同周期性和结构特征的重金属染色原纤维。我们得出结论,100纳米周期性细丝和原纤维代表VI型胶原的天然聚集形式。很可能多年来许多观察者在广泛的正常和病理组织中报道的具有相同周期性和外观的带状原纤维至少部分是VI型胶原。