Leardkamolkarn V, Abrahamson D R
Department of Cell Biology and Anatomy, University of Alabama at Birmingham 35294.
Cell Tissue Res. 1988 Jan;251(1):171-81. doi: 10.1007/BF00215462.
To determine whether circulating antibodies against laminin can bind in vivo to basement membranes within endocrine glands, affinity-purified sheep or rabbit anti-laminin IgG was intravenously injected into rats. One to five hours after injection, anti-laminin IgG was bound to all basement membranes of adrenal and anterior pituitary glands of mature as well as 2-day-old newborn rats as shown by immunofluorescence microscopy. After the injection of anti-laminin conjugated directly to horseradish peroxidase (HRP), HRP reaction product was also present throughout adrenal and pituitary basement membranes in mature and immature glands 1-5 h post-injection. Ultrathin Lowicryl sections from rats that received unconjugated rabbit anti-laminin IgG 1 h prior to fixation with paraformaldehyde were labeled directly with anti-rabbit IgG-colloidal gold. In these cases, gold also bound specifically over the lamina densa and lamina rara. When adrenal or pituitary glands from mature rats were examined by immunofluorescence 1 week after the injection of sheep anti-laminin IgG, the patterns and amounts of bound sheep IgG were indistinguishable from those observed 1 h after injection. In contrast, significantly less fluorescence was present in glands from 7-day-old rat pups that had received anti-laminin IgG 5 days earlier. In addition, when anti-laminin IgG-HRP was injected into newborns and glands were fixed 5 days later, lengths of labeled endothelial and epithelial basement membranes were often interspersed with unlabeled lengths in zones of cellular proliferation in the outer adrenal cortex and throughout the pituitary gland. These results indicated that unlabeled basement membranes in these regions were probably assembled after the injection of anti-laminin IgG, which would also explain diminished labeling of basement membranes in these animals. Despite the continued presence of heterologous anti-laminin IgG within endocrine basement membranes, however, rat IgG, rat C3, inflammatory cells, or histologic abnormalities were observed in neither newborn nor adult glands under the conditions examined here. Sections from rats injected with control IgG or control IgG-HRP were entirely negative by immunofluorescence, immunoperoxidase, and immunogold techniques. We therefore conclude that (1) apparently large amounts of circulating anti-laminin IgG can bind to adrenal and pituitary basement membranes, and (2) at least some of these basement membranes are assembled during development by progressive splicing of newly synthesized matrix into that already present.
为了确定循环中的抗层粘连蛋白抗体在体内是否能与内分泌腺内的基底膜结合,将亲和纯化的羊或兔抗层粘连蛋白IgG静脉注射到大鼠体内。注射后1至5小时,免疫荧光显微镜检查显示,抗层粘连蛋白IgG与成熟及2日龄新生大鼠肾上腺和垂体前叶的所有基底膜结合。注射直接与辣根过氧化物酶(HRP)偶联的抗层粘连蛋白后,在注射后1 - 5小时,成熟和未成熟腺体的肾上腺和垂体基底膜中也均存在HRP反应产物。在用多聚甲醛固定前1小时接受未偶联兔抗层粘连蛋白IgG的大鼠超薄Lowicryl切片,直接用抗兔IgG - 胶体金标记。在这些情况下,金也特异性地结合在致密层和稀疏层上。当在注射羊抗层粘连蛋白IgG 1周后通过免疫荧光检查成熟大鼠的肾上腺或垂体时,结合的羊IgG的模式和数量与注射后1小时观察到的无明显差异。相比之下,5天前接受抗层粘连蛋白IgG的7日龄幼鼠腺体中的荧光明显较少。此外,当将抗层粘连蛋白IgG - HRP注射到新生大鼠体内并在5天后固定腺体时,在外肾上腺皮质和整个垂体的细胞增殖区域,标记的内皮和上皮基底膜的长度常常与未标记的长度相间分布。这些结果表明,这些区域中未标记的基底膜可能是在注射抗层粘连蛋白IgG后组装的,这也可以解释这些动物中基底膜标记减少的原因。然而,尽管内分泌基底膜中持续存在异源抗层粘连蛋白IgG,但在此处检查的条件下,在新生或成年腺体中均未观察到大鼠IgG、大鼠C3、炎性细胞或组织学异常。注射对照IgG或对照IgG - HRP的大鼠切片通过免疫荧光、免疫过氧化物酶和免疫金技术检测均呈完全阴性。因此,我们得出结论:(1)显然大量循环的抗层粘连蛋白IgG能与肾上腺和垂体基底膜结合;(2)这些基底膜中至少有一些是在发育过程中通过将新合成的基质逐步拼接至已存在的基质中而组装形成的。