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多发性骨骺发育不良,费尔班克型:软骨的形态学和生物化学研究

Multiple epiphyseal dysplasia, Fairbank type: morphologic and biochemical study of cartilage.

作者信息

Stanescu R, Stanescu V, Muriel M P, Maroteaux P

机构信息

Hôpital des Enfants-Malades, Paris, France.

出版信息

Am J Med Genet. 1993 Feb 15;45(4):501-7. doi: 10.1002/ajmg.1320450420.

Abstract

We have performed histochemical, immunohistochemical, electron microscopic, and biochemical studies on the upper tibial cartilage from a case of multiple epiphyseal dysplasia, Fairbank type. Most chondrocytes had intracytoplasmic inclusions which took the stains for proteins and were resistant to microbial collagenase digestion. The electron microscopic study showed that the inclusions are dilatations of the rough endoplasmic reticulum containing a material with alternately wide electron dense and electron lucent layers. Both in optical and in electron microscopy the inclusions fixed antibodies against the core protein of the large cartilage proteoglycans (aggrecans). They didn't stain with antibodies against type II collagen. The gel electrophoretic pattern of the large proteoglycans was different from normal controls. The morphologic and biochemical alterations found in multiple epiphyseal dysplasia are similar to those already described in pseudoachondroplasia (Stanescu et al.: Eur J Pediatr 138:121-225, 1982; Stanescu et al.: J Bone Joint Surg 66A:817-836, 1984). However, the inclusions are smaller and the growth cartilage much less disorganized in multiple epiphyseal dysplasia. The similarity of morphologic and biochemical abnormalities strongly suggests that the two diseases have a similar pathogenesis and belong to the same bone dysplasia family.

摘要

我们对一例Fairbank型多发性骨骺发育不良患者的胫骨上段软骨进行了组织化学、免疫组织化学、电子显微镜及生物化学研究。多数软骨细胞有胞质内包涵体,其对蛋白质染色呈阳性,且对微生物胶原酶消化有抗性。电子显微镜研究显示,这些包涵体是粗面内质网的扩张,内含一种具有交替出现的宽电子致密层和电子透亮层的物质。在光学显微镜和电子显微镜下,这些包涵体均能结合针对大型软骨蛋白聚糖(聚集蛋白聚糖)核心蛋白的抗体。它们不能与抗II型胶原的抗体染色。大型蛋白聚糖的凝胶电泳图谱与正常对照不同。在多发性骨骺发育不良中发现的形态学和生物化学改变与已在假性软骨发育不全中描述的改变相似(斯坦内斯库等人:《欧洲儿科学杂志》138:121 - 225,1982年;斯坦内斯库等人:《骨与关节外科杂志》66A:817 - 836,1984年)。然而,在多发性骨骺发育不良中,包涵体较小,生长中的软骨组织紊乱程度也低得多。形态学和生物化学异常的相似性强烈提示这两种疾病有相似的发病机制,且属于同一骨发育不良家族。

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