FARQUHAR M G, WISSIG S L, PALADE G E
J Exp Med. 1961 Jan 1;113(1):47-66. doi: 10.1084/jem.113.1.47.
Ferritin was used as a tracer to investigate pathways and mechanisms for transfer across the various layers of the glomerular capillary wall. Kidney tissue, fixed at intervals of 2 minutes to 2 hours following an intravenous injection of ferritin, was examined by electron microscopy. The observations confirmed the existence of three distinct and successive layers in the glomerular capillary wall (the endothelium, the basement membrane, and the visceral epithelium). In addition, they demonstrated a number of new structural features: namely (a) discrete fibrils in the subendothelial spaces; (b) a characteristic, highly elaborate, cytoplasmic organization in the visceral epithelium; and (c) special structures resembling "desmosomes" in the slits between foot processes. In animals sacrificed at short time intervals (2 to 15 minutes) following ferritin administration, ferritin molecules were found at high concentration in the lumen and endothelial fenestrae, at low concentration in the basement membrane, and in very small numbers within the epithelium. Later (1 to 2 hours), the tracer particles were still present in the lumen and within endothelial fenestrae, and, in addition, had accumulated on the luminal side of the basement membrane, especially in the axial regions of the vessels. Larger numbers of ferritin molecules were also found in the epithelium-in invaginations of the cell membrane at the base of the foot processes, and in various membrane-limited bodies (vesicles, multivesicular bodies, vacuoles, and dense bodies) present within the cytoplasm. These observations suggest that the endothelial fenestrae are patent and that the basement membrane is the main filtration barrier. Since the basement membrane has no demonstrable pores, it is probably not a simple sieve but presumably is a gel-like structure with two fine fibrillar components embedded in an amorphous matrix. Both the epithelium and endothelium may be concerned with building and maintaining this structure. Finally, the intracellular accumulation of particles in the epithelium suggests that the latter acts as a monitor that recovers, at least in part, the small amounts of protein which normally leak through the filter.
铁蛋白被用作示踪剂,以研究其穿过肾小球毛细血管壁各层的途径和机制。在静脉注射铁蛋白后,每隔2分钟至2小时固定一次肾脏组织,通过电子显微镜进行检查。观察结果证实了肾小球毛细血管壁中存在三个不同且连续的层(内皮、基底膜和脏层上皮)。此外,还发现了一些新的结构特征:即(a)内皮下间隙中的离散纤维;(b)脏层上皮中具有特征性的、高度精细的细胞质组织;(c)足突之间裂隙中类似“桥粒”的特殊结构。在给予铁蛋白后短时间间隔(2至15分钟)处死的动物中,发现铁蛋白分子在管腔和内皮窗孔中浓度较高,在基底膜中浓度较低,在上皮内数量极少。之后(1至2小时),示踪颗粒仍存在于管腔和内皮窗孔内,此外,还在基底膜的管腔侧积聚,尤其是在血管的轴向区域。在足突基部的细胞膜内陷处以及细胞质中存在的各种膜性细胞器(囊泡、多囊泡体、液泡和致密体)中也发现了大量铁蛋白分子。这些观察结果表明内皮窗孔是开放的,基底膜是主要的滤过屏障。由于基底膜没有可证实的孔隙,它可能不是一个简单的筛子,大概是一种凝胶状结构,有两种细纤维成分嵌入无定形基质中。上皮和内皮都可能参与构建和维持这种结构。最后,上皮内颗粒的细胞内积聚表明,上皮起到了监测器的作用,至少部分地回收了通常漏过滤器的少量蛋白质。