Abrahamson D R
J Cell Biol. 1985 Jun;100(6):1988-2000. doi: 10.1083/jcb.100.6.1988.
To examine the origin and assembly of glomerular basement membranes (GBMs), affinity purified anti-laminin IgG was directly coupled to horseradish peroxidase (HRP) and intravenously injected into newborn rats. Kidneys were then processed for peroxidase histochemistry and microscopy. Within 1 h after injection, anti-laminin bound to basement membranes of nephrons in all developmental stages (vesicle, comma, S-shaped, developing capillary loop, and maturing glomeruli). In S-shaped and capillary loop glomeruli, anti-laminin-HRP labeled a double basal lamina between the endothelium and epithelium. Sections incubated with anti-laminin in vitro showed labeling within the rough endoplasmic reticulum of endothelium and epithelium, indicating that both cell types synthesized laminin for the double basement membrane. In maturing glomeruli, injected anti-laminin-HRP bound throughout the GBMs, and double basement membranes were rarely observed. At this stage, however, numerous knobs or outpockets of basement membrane material extending far into the epithelial side of the capillary wall were identified and these were also labeled throughout their full thickness. No such outpockets were found in the endothelial cell layer of newborn rats (and they normally are completely absent in fully mature, adult glomeruli). In contrast with these results, in kidneys fixed 4-6 d after anti-laminin IgG-HRP injection, basement membranes of vesicle, comma, and S-shaped nephrons were unlabeled, indicating that they were assembled after injection. GBM labeling was seen in maturing glomeruli, however. In addition, the outpockets of basement membrane extending into the epithelium were often completely unlabeled whereas GBMs lying immediately beneath them were labeled intensely, which indicates that the outpockets were probably assembled by the epithelium. Injections of sheep anti-laminin IgG followed 8 d later with injections of biotin-rabbit anti-laminin IgG and double-label immunofluorescence microscopy confirmed that GBM formation continued during individual capillary loop expansion. GBM assembly therefore occurs by at least two different processes at separate times in development: (a) fusion of endothelial and epithelial basement membranes followed by (b) addition of new basement membrane from the epithelium into existing GBMs.
为了研究肾小球基底膜(GBM)的起源和组装,将亲和纯化的抗层粘连蛋白IgG直接与辣根过氧化物酶(HRP)偶联,并静脉注射到新生大鼠体内。然后对肾脏进行过氧化物酶组织化学和显微镜检查。注射后1小时内,抗层粘连蛋白与所有发育阶段(囊泡、逗号、S形、发育中的毛细血管袢和成熟肾小球)的肾单位基底膜结合。在S形和毛细血管袢肾小球中,抗层粘连蛋白-HRP标记了内皮细胞和上皮细胞之间的双层基底膜。在体外与抗层粘连蛋白孵育的切片显示,内皮细胞和上皮细胞的粗面内质网内有标记,表明这两种细胞类型都为双层基底膜合成层粘连蛋白。在成熟肾小球中,注射的抗层粘连蛋白-HRP结合在整个GBM中,很少观察到双层基底膜。然而,在这个阶段,发现许多基底膜物质的结节或袋状结构延伸到毛细血管壁的上皮侧很远,并且这些结构在其整个厚度上都有标记。在新生大鼠的内皮细胞层中未发现此类袋状结构(并且在完全成熟的成年肾小球中通常完全不存在)。与这些结果相反,在注射抗层粘连蛋白IgG-HRP后4-6天固定的肾脏中,囊泡、逗号和S形肾单位的基底膜未被标记,表明它们是在注射后组装的。然而,在成熟肾小球中可见GBM标记。此外,延伸到上皮细胞的基底膜袋状结构通常完全未被标记,而紧挨着它们的GBM则被强烈标记,这表明这些袋状结构可能是由上皮细胞组装的。在注射羊抗层粘连蛋白IgG 8天后,再注射生物素-兔抗层粘连蛋白IgG,并通过双标记免疫荧光显微镜证实,在单个毛细血管袢扩张过程中GBM形成仍在继续。因此,GBM组装在发育过程中的不同时间至少通过两种不同的过程发生:(a)内皮细胞和上皮细胞基底膜融合,随后(b)上皮细胞将新的基底膜添加到现有的GBM中。