Labat-Robert J, Robert L
Laboratoire de recherche ophtalmologique, hôpital Hôtel-Dieu, université Paris-5, 1, place du Parvis-Notre-Dame, 75181 Paris cedex 04, France.
Pathol Biol (Paris). 2012 Feb;60(1):66-75. doi: 10.1016/j.patbio.2011.11.010. Epub 2012 Jan 9.
During decades preceding and following the last war, a favourite subject of biochemists was to study glycoproteins. One class of these substances, found in connective tissues were characterised as polysaccharides, most of them found to be linked to proteins, designated later as glycosaminoglycans and proteoglycans. Another family of glycoconjugates represented epithelial mucins as found in the gastro-intestinal and respiratory tracts and conduits. A third family of glycoconjugates is represented by circulating glycoproteins isolated from the blood plasma, mostly studied by medical biochemists in relation to pathological conditions comprising those increasing during the inflammatory reaction: acute phase glycoproteins. Their study suggested that they might be derived from connective tissues. Although inflammatory glycoproteins derive mostly from the liver, the possibility of connective tissue origin of glycoproteins remained open. Using cornea, an avascular tissue, we could show that connective tissues also synthesize glycoproteins. We proposed to designate them "structural glycoproteins" (SGP-s) to distinguish them from circulating, blood-born glycoproteins coming from the liver. They play locally "structural" roles in connective tissues where they are synthesized. Soon after fibronectin was identified and shown to mediate cell-matrix interactions. A large family of glycoproteins were then isolated from a variety of sources, cells, tissues others than liver, confirming our original hypothesis. The first experiments on these glycoproteins were published from 1961/1962 giving the opportunity to recapitulate this biochemical adventure 50 years later, together with the celebration of the foundation of the first connective tissue society in Europe, as described in the first article in this issue.
在上次战争之前及之后的几十年里,糖蛋白一直是生物化学家们喜爱的研究对象。这类物质中的一类存在于结缔组织中,其特征为多糖,其中大多数被发现与蛋白质相连,后来被命名为糖胺聚糖和蛋白聚糖。另一类糖缀合物是存在于胃肠道、呼吸道及导管中的上皮粘蛋白。第三类糖缀合物是从血浆中分离出的循环糖蛋白,医学 Biochemists 大多针对包括炎症反应中增加的那些病症的病理状况对其进行研究:急性期糖蛋白。对它们的研究表明,它们可能源自结缔组织。尽管炎性糖蛋白大多源自肝脏,但糖蛋白源自结缔组织的可能性仍然存在。利用角膜这一无血管组织,我们能够证明结缔组织也能合成糖蛋白。我们提议将它们命名为“结构糖蛋白”(SGP - s),以将它们与源自肝脏的循环血源性糖蛋白区分开来。它们在合成它们的结缔组织中发挥局部“结构”作用。纤连蛋白被鉴定并证明能介导细胞 - 基质相互作用后不久。随后从多种来源(除肝脏外的细胞、组织等)分离出了一大类糖蛋白,证实了我们最初的假设。关于这些糖蛋白的首批实验于1961/1962年发表,这使得50年后有机会回顾这段生化历程,同时庆祝欧洲第一个结缔组织协会的成立,正如本期第一篇文章中所描述的那样。