Góes Rejane M, Nader Helena B, Porcionatto Marimelia A, Haddad Antonio, Laicine Eduardo M
Departamento de Biologia, UNESP, São José do Rio Preto, Brazil.
Curr Eye Res. 2005 May;30(5):405-13. doi: 10.1080/02713680590934148.
To characterize the vitreous intrinsic proteoglycans, investigate their dynamics, and examine their role in the supramolecular organization of the vitreous.
Vitreous from normal rabbits was collected and processed for observation with the transmission electron microscope after treatment with glycosidases. Also, rabbits were injected intravitreally with [35S]-sodium sulfate and sacrificed at several time intervals after the injection. Proteoglycans (PGs) were assayed in the vitreous supernatant or in whole samples extracted with guanidine hydrochloride by polyacrylamide or agarose gel electrophoresis, followed respectively by fluorography or autoradiography, and ion-exchange chromatography and gel-filtration chromatography, combined with glycolytic treatment of the samples. The sulfated glycosaminoglycans (GAGs) were characterized by agarose gel electrophoresis after treating vitreous samples with protease and specific glycosidases.
The electron microscopic study revealed a network with hyaluronic acid (HA) as thin threads coating and connecting collagen fibrils. The elimination of the HA coat showed chondroitin sulfate granules (8-25 nm) arranged at regular intervals on the fibril surface. The chondroitinase ABC digestion, besides removing the granules, also caused the formation of thicker bundles of the collagen fibrils. The PG and GAG analysis indicated that there are three renewable PGs in the vitreous (e.g., one heparan- and two chondroitin-sulfate ones).
At least one of the chondroitin sulfate PGs is involved in the interactions that occur in the vitreous structure, mainly by providing adequate spacing between the collagen fibrils, a condition that is probably required for the transparency of the vitreous.
鉴定玻璃体的固有蛋白聚糖,研究其动态变化,并探讨其在玻璃体超分子结构中的作用。
收集正常兔的玻璃体,用糖苷酶处理后进行透射电子显微镜观察。此外,给兔玻璃体内注射[35S] - 硫酸钠,并在注射后的几个时间间隔处死动物。通过聚丙烯酰胺或琼脂糖凝胶电泳分别对玻璃体上清液或用盐酸胍提取的全样本中的蛋白聚糖(PGs)进行分析,随后分别进行荧光显影或放射自显影,以及离子交换色谱和凝胶过滤色谱,并结合样本的糖酵解处理。在用蛋白酶和特定糖苷酶处理玻璃体样本后,通过琼脂糖凝胶电泳对硫酸化糖胺聚糖(GAGs)进行鉴定。
电子显微镜研究显示,以透明质酸(HA)为细丝形成的网络包裹并连接着胶原纤维。去除HA包衣后,可见硫酸软骨素颗粒(8 - 25纳米)以规则间隔排列在纤维表面。硫酸软骨素酶ABC消化不仅去除了颗粒,还导致胶原纤维形成更粗的束状结构。PG和GAG分析表明,玻璃体中有三种可再生的PG(例如,一种硫酸乙酰肝素和两种硫酸软骨素)。
至少有一种硫酸软骨素PG参与了玻璃体结构中的相互作用,主要是通过在胶原纤维之间提供足够的间距,这可能是玻璃体透明所必需的条件。