Bruns R R, Palade G E
J Cell Biol. 1968 May;37(2):277-99. doi: 10.1083/jcb.37.2.277.
The pathway by which intravenously injected ferritin molecules move from the blood plasma across the capillary wall has been investigated in the muscle of the rat diaphragm. At 2 min after administration, the ferritin molecules are evenly distributed in high concentration in the blood plasma of capillaries and occur within vesicles along the blood front of the endothelium. At the 10-min time point, a small number of molecules appear in the adventitia, and by 60 min they are relatively numerous in the adventitia and in phagocytic vesicles and vacuoles of adventitial macrophages. Thereafter, the amount of ferritin in the adventitia and pericapillary regions gradually increases so that at 1 day the concentration in the extracellular spaces approaches that in the blood plasma. Macrophages and, to a lesser extent, fibroblasts contain large amounts of ferritin. 4 days after administration, ferritin appears to be cleared from the blood and from the capillary walls, but it still persists in the adventitial macrophages and fibroblasts. At all time points examined, ferritin molecules within the endothelial tunic were restricted to vesicles or to occasional multivesicular or dense bodies; they were not found in intercellular junctions or within the cytoplasmic matrix. Ferritin molecules did not accumulate within or against the basement membranes. Over the time period studied, the concentration of ferritin in the blood decreased, first rapidly, then slowly, in two apparently exponential phases. Liver and spleen removed large amounts of ferritin from the blood. Diaphragms fixed at time points from 10 min to 1 day, stained for iron by the Prussian Blue method, and prepared as cleared whole mounts, showed a progressive and even accumulation of ferritin in adventitial macrophages along the entire capillary network. These findings indicate: (1) that endothelial cell vesicles are the structural equivalent of the large pore system postulated in the pore theory of capillary permeability; (2) that the basement membrane is not a structural restraint in the movement of ferritin molecules across the capillary wall; (3) that transport of ferritin occurs uniformly along the entire length of the capillary; and (4) that the adventitial macrophages monitor the capillary filtrate and partially clear it of the tracer.
已在大鼠膈肌肌肉中研究了静脉注射的铁蛋白分子从血浆穿过毛细血管壁的途径。给药后2分钟,铁蛋白分子以高浓度均匀分布在毛细血管的血浆中,并出现在内皮细胞血液前沿的囊泡内。在10分钟时间点,少量分子出现在外膜中,到60分钟时,它们在外膜以及外膜巨噬细胞的吞噬囊泡和液泡中相对较多。此后,外膜和毛细血管周围区域中铁蛋白的量逐渐增加,因此在1天时细胞外空间中的浓度接近血浆中的浓度。巨噬细胞以及程度较轻的成纤维细胞含有大量铁蛋白。给药4天后,铁蛋白似乎已从血液和毛细血管壁中清除,但仍存在于外膜巨噬细胞和成纤维细胞中。在所有检查的时间点,内皮细胞层内的铁蛋白分子仅限于囊泡或偶尔的多囊泡或致密体;它们未在细胞间连接或细胞质基质中发现。铁蛋白分子没有在基底膜内或基底膜上积聚。在所研究的时间段内,血液中铁蛋白的浓度下降,首先迅速下降,然后缓慢下降,呈两个明显的指数阶段。肝脏和脾脏从血液中清除了大量铁蛋白。在10分钟至1天的时间点固定的膈肌,用普鲁士蓝法进行铁染色,并制备成透明整装片,显示沿整个毛细血管网络外膜巨噬细胞中铁蛋白逐渐均匀积累。这些发现表明:(1)内皮细胞囊泡相当于毛细血管通透性孔理论中假设的大孔系统;(2)基底膜不是铁蛋白分子穿过毛细血管壁的结构限制;(3)铁蛋白的运输沿毛细血管的整个长度均匀发生;(4)外膜巨噬细胞监测毛细血管滤液并部分清除其中的示踪剂。