Sage H, Tupper J, Bramson R
J Cell Physiol. 1986 Jun;127(3):373-87. doi: 10.1002/jcp.1041270305.
A novel, serum albumin-binding glycoprotein of molecular weight (mw) 43,000 (43K protein) was initially purified from the culture medium of bovine aortic endothelial (BAE) cells (Sage, H., Johnson, C., and Bornstein, P., J. Biol. Chem. 259:3993-4007, 1984). Its secretion by normal mesenchymal cells and by transformed cells of both ectodermal and endodermal origin suggested a general role in cellular function. To examine the effect of sublethal injury in vitro on the biosynthesis of 43K protein, BAE cells were exposed to endotoxin. At concentrations which produced minimal cell detachment and lysis, the cells secreted 70-100% more protein compared to control cultures, and the relative increase in 43K protein over total protein was approximately three-fold. A second type of cellular injury, manifested by rapid cellular proliferation and migration in response to sparse plating density (a condition that we have termed 'culture shock'), was also accompanied by a significant increase in the secretion of 43K protein. Pulse-chase studies revealed that the initial product secreted within 1.5 h was of Mr 38,000, and that between 6 and 21 h this molecule was converted to the final form of Mr 43,000. The 43K protein was not associated with RNA or glycosaminoglycan, but appeared to be linked to complex oligosaccharides containing peripheral sialosyl residues. Treatment with tunicamycin produced lower mw forms that displayed reduced affinity for albumin. By immunologic criteria, peptide mapping, and amino acid analysis, the 43K protein was shown to be structurally distinct from several proteins of Mr 40,000-50,000 associated with endothelium or with serum, including tissue factor, a plasminogen anti-activator, and several apolipoproteins. In addition, the 43K protein was not present in the extracellular matrices of endothelial, fibroblastic, or smooth muscle cells, nor was it found in plasma, serum, platelet releasate, or alveolar lavage fluids. These studies identify a unique Mr 43,000 glycoprotein that is associated with cellular stress or injury in vitro. As a secreted but nonmatrix macromolecule, this protein may be part of a 'survival kit' used by the endothelium to cope with cellular injury.
一种分子量为43000的新型血清白蛋白结合糖蛋白(43K蛋白)最初是从牛主动脉内皮(BAE)细胞的培养基中纯化出来的(塞奇,H.,约翰逊,C.,和博恩斯坦,P.,《生物化学杂志》259:3993 - 4007,1984)。它由正常间充质细胞以及外胚层和内胚层来源的转化细胞分泌,这表明其在细胞功能中具有普遍作用。为了研究体外亚致死性损伤对43K蛋白生物合成的影响,将BAE细胞暴露于内毒素。在产生最小细胞脱离和裂解的浓度下,与对照培养物相比,细胞分泌的蛋白质增加了70 - 100%,并且43K蛋白相对于总蛋白的相对增加约为三倍。第二种类型的细胞损伤表现为细胞对稀疏接种密度的快速增殖和迁移(我们将这种情况称为“培养休克”),同时43K蛋白的分泌也显著增加。脉冲追踪研究表明,在1.5小时内分泌的初始产物分子量为38000,并且在6至21小时之间该分子转化为最终形式的分子量43000。43K蛋白不与RNA或糖胺聚糖相关,但似乎与含有外周唾液酸残基的复杂寡糖相连。用衣霉素处理产生了分子量较低的形式,其对白蛋白的亲和力降低。通过免疫学标准、肽图谱分析和氨基酸分析,43K蛋白在结构上与几种分子量为40000 - 50000且与内皮或血清相关的蛋白质不同,包括组织因子、纤溶酶原抗激活剂和几种载脂蛋白。此外,43K蛋白不存在于内皮细胞、成纤维细胞或平滑肌细胞的细胞外基质中,也不存在于血浆、血清、血小板释放物或肺泡灌洗液中。这些研究鉴定出一种独特的分子量43000的糖蛋白,它在体外与细胞应激或损伤相关。作为一种分泌型但非基质大分子,这种蛋白可能是内皮细胞用于应对细胞损伤的“生存工具包”的一部分。