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视黄醇对琼脂糖培养的人软骨细胞的影响。

Influence of retinol on human chondrocytes in agarose culture.

作者信息

Aulthouse A L, Carubelli C M, Dow T M, Ziegelmayer C, Beck M

机构信息

University of Oklahoma Health Sciences Center, College of Medicine, Department of Anatomical Sciences 73190.

出版信息

Anat Rec. 1992 Jan;232(1):52-9. doi: 10.1002/ar.1092320107.

Abstract

Vitamin A and its congeners, collectively called retinoids, are known to have teratogenic potential and have induced craniofacial and limb malformations in numerous animal species. More importantly, retinoids are recognized as teratogenic to fetuses of pregnant women who have taken such preparations for dermatologic disorders. Information gathered from the study of animal models suggests that retinoids interfere with cartilage differentiation. If chondrogenesis in limb development is disturbed it may contribute to limb reductions and malformations. In vitro studies using various animal systems have shown that cartilage matrix macromolecules are altered to resemble those secreted by mesenchymal cells. The response of human chondrocytes to retinoids in vitro is not known. Culture of human chondrocytes in agarose maintains the cartilage phenotype and therefore serves as a model system to evaluate the influence of retinoids directly on human chondrogenesis. The studies presented in this paper were done to determine if the expression of specific matrix macromolecules of human chondrocytes in agarose culture is altered by retinol treatment. Immunocytochemistry demonstrated enhanced labeling of type I collagen while type II collagen labeling was reduced in cultures treated with retinol. In addition, morphometric analyses indicated a decrease in the size and number of chondrogenic clusters and that individual cells synthesized less alcian blue matrix when compared to parallel control cultures. The size of the proteoglycan monomers, glycosaminoglycan side chains as well as the disaccharide composition were not affected. However, there was a reduction in the quantity of proteoglycan monomers produced.

摘要

维生素A及其同类物统称为类视黄醇,已知具有致畸潜力,并在众多动物物种中诱发了颅面和肢体畸形。更重要的是,类视黄醇被认为对服用此类制剂治疗皮肤病的孕妇的胎儿具有致畸性。从动物模型研究中收集的信息表明,类视黄醇会干扰软骨分化。如果肢体发育中的软骨形成受到干扰,可能会导致肢体发育不全和畸形。使用各种动物系统进行的体外研究表明,软骨基质大分子会发生改变,类似于间充质细胞分泌的大分子。人类软骨细胞在体外对类视黄醇的反应尚不清楚。在琼脂糖中培养人类软骨细胞可维持软骨表型,因此可作为评估类视黄醇对人类软骨形成直接影响的模型系统。本文所呈现的研究旨在确定在琼脂糖培养中,视黄醇处理是否会改变人类软骨细胞特定基质大分子的表达。免疫细胞化学显示,在用视黄醇处理的培养物中,I型胶原蛋白的标记增强,而II型胶原蛋白的标记减少。此外,形态计量分析表明,与平行对照培养物相比,软骨形成簇的大小和数量减少,单个细胞合成的阿尔新蓝基质减少。蛋白聚糖单体的大小、糖胺聚糖侧链以及二糖组成均未受影响。然而,产生的蛋白聚糖单体数量有所减少。

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