Elvevold Kjetil H, Nedredal Geir I, Revhaug Arthur, Smedsrød Bård
Department of Experimental Pathology, Institute of Medical Biology, University of Tromsø, 9038 Tromsø, Norway.
Comp Hepatol. 2004 Aug 12;3(1):4. doi: 10.1186/1476-5926-3-4.
The liver sinusoidal endothelial cells (LSEC) and Kupffer cells constitute the most powerful scavenger system in the body. Various waste macromolecules, continuously released from tissues in large quantities as a consequence of normal catabolic processes are cleared by the LSEC. In spite of the fact that pig livers are used in a wide range of experimental settings, the scavenger properties of pig LSEC has not been investigated until now. Therefore, we studied the endocytosis and intracellular transport of ligands for the five categories of endocytic receptors in LSEC. RESULTS: Endocytosis of five 125I-labelled molecules: collagen alpha-chains, FITC-biotin-hyaluronan, mannan, formaldehyde-treated serum albumin (FSA), and aggregated gamma globulin (AGG) was substantial in cultured LSEC. The endocytosis was mediated via the collagen-, hyaluronan-, mannose-, scavenger-, or IgG Fc-receptors, respectively, as judged by the ability of unlabelled ligands to compete with labelled ligands for uptake. Intracellular transport was studied employing a morphological pulse-chase technique. Ninety minutes following administration of red TRITC-FSA via the jugular vein of pigs to tag LSEC lysosomes, cultures of the cells were established, and pulsed with green FITC-labelled collagen, -mannan, and -FSA. By 10 min, the FITC-ligands was located in small vesicles scattered throughout the cytoplasm, with no co-localization with the red lysosomes. By 2 h, the FITC-ligands co-localized with red lysosomes. When LSEC were pulsed with FITC-AGG and TRITC-FSA together, co-localization of the two ligands was observed following a 10 min chase. By 2 h, only partial co-localization was observed; TRITC-FSA was transported to lysosomes, whereas FITC-AGG only slowly left the endosomes. Enzyme assays showed that LSEC and Kupffer cells contained equal specific activities of hexosaminidase, aryl sulphates, acid phosphatase and acid lipase, whereas the specific activities of alpha-mannosidase, and glucuronidase were higher in LSEC. All enzymes measured showed considerably higher specific activities in LSEC compared to parenchymal cells. CONCLUSION: Pig LSEC express the five following categories of high capacity endocytic receptors: scavenger-, mannose-, hyaluronan-, collagen-, and IgG Fc-receptors. In the liver, soluble ligands for these five receptors are endocytosed exclusively by LSEC. Furthermore, LSEC contains high specific activity of lysosomal enzymes needed for degradation of endocytosed material. Our observations suggest that pig LSEC have the same clearance activity as earlier described in rat LSEC.
肝窦内皮细胞(LSEC)和库普弗细胞构成了体内最强大的清除系统。正常分解代谢过程中组织持续大量释放的各种废弃大分子由LSEC清除。尽管猪肝在广泛的实验环境中被使用,但迄今为止猪LSEC的清除特性尚未得到研究。因此,我们研究了LSEC中五类内吞受体配体的内吞作用和细胞内转运。
在培养的LSEC中,五种125I标记分子:胶原α链、异硫氰酸荧光素-生物素-透明质酸、甘露聚糖、甲醛处理的血清白蛋白(FSA)和聚集的γ球蛋白(AGG)的内吞作用显著。根据未标记配体与标记配体竞争摄取的能力判断,内吞作用分别通过胶原、透明质酸、甘露糖、清道夫或IgG Fc受体介导。采用形态学脉冲追踪技术研究细胞内转运。通过猪颈静脉注射红色四甲基罗丹明异硫氰酸盐标记的FSA以标记LSEC溶酶体90分钟后,建立细胞培养物,并用绿色异硫氰酸荧光素标记的胶原、甘露聚糖和FSA进行脉冲处理。到10分钟时,异硫氰酸荧光素标记物位于分散在整个细胞质中的小泡中,与红色溶酶体无共定位。到2小时时,异硫氰酸荧光素标记物与红色溶酶体共定位。当LSEC同时用异硫氰酸荧光素标记的AGG和四甲基罗丹明异硫氰酸盐标记的FSA进行脉冲处理时,追踪10分钟后观察到两种配体的共定位。到2小时时,仅观察到部分共定位;四甲基罗丹明异硫氰酸盐标记的FSA被转运到溶酶体,而异硫氰酸荧光素标记的AGG仅缓慢离开内体。酶分析表明,LSEC和库普弗细胞中己糖胺酶、芳基硫酸酯酶、酸性磷酸酶和酸性脂肪酶的比活性相等,而α-甘露糖苷酶和葡糖醛酸酶的比活性在LSEC中更高。与实质细胞相比,所有检测的酶在LSEC中的比活性都显著更高。
猪LSEC表达以下五类高容量内吞受体:清道夫、甘露糖、透明质酸、胶原和IgG Fc受体。在肝脏中,这五种受体的可溶性配体仅由LSEC内吞。此外,LSEC含有降解内吞物质所需的高比活性溶酶体酶。我们的观察结果表明,猪LSEC具有与先前在大鼠LSEC中描述的相同的清除活性。