Aulthouse A L, Alroy J
Department of Anatomical Sciences, College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, USA.
Virchows Arch. 1995;426(2):135-40. doi: 10.1007/BF00192634.
Lysosomal storage diseases such as GM1-gangliosidosis are associated with skeletal abnormalities. Radiological and histological studies, both in human and corresponding animal models, indicate retarded bone formation. Since cartilage maturation leads to bone formation, we developed an in vitro system to study and compare the biological features of cartilage from dogs affected with GM1-gangliosidosis with age-matched controls. Costochondral chondrocytes were grown in monolayer and in agarose culture. Both affected and control cells dedifferentiated in monolayer; however, in agarose culture they re-expressed the chondrocytic phenotype. Cells from affected dogs were enlarged and contained numerous large vacuoles when compared with control cells. This morphology was similar to that seen in vivo. In addition, the affected cells appeared to have a reduction in mitosis and alcian blue staining proteoglycans. Cultures from affected animals contained fewer cells positive for alkaline phosphatase activity. Both affected and control cells expressed collagen types I and II and were positive for the lectin Ricinus communis agglutinin-I. However, the staining of the control culture for type II collagen was more prominent than in the affected cells. These findings suggest that culture of chondrocytes in agarose may be a useful method for studying the biology of cartilage which leads to skeletal abnormalities in lysosomal storage diseases.
诸如GM1神经节苷脂贮积症之类的溶酶体贮积病与骨骼异常有关。在人类和相应动物模型中进行的放射学和组织学研究均表明骨形成延迟。由于软骨成熟会导致骨形成,我们开发了一种体外系统,用于研究和比较患有GM1神经节苷脂贮积症的犬的软骨与年龄匹配的对照犬软骨的生物学特征。肋软骨细胞在单层培养和琼脂糖培养中生长。受影响的细胞和对照细胞在单层培养中均发生去分化;然而,在琼脂糖培养中它们重新表达了软骨细胞表型。与对照细胞相比,患病犬的细胞增大且含有大量大液泡。这种形态与在体内观察到的相似。此外,受影响的细胞似乎有丝分裂减少,阿尔辛蓝染色的蛋白聚糖也减少。患病动物的培养物中碱性磷酸酶活性阳性的细胞较少。受影响的细胞和对照细胞均表达I型和II型胶原蛋白,并且对蓖麻凝集素-I呈阳性。然而,对照培养物中II型胶原蛋白的染色比受影响的细胞中更明显。这些发现表明,在琼脂糖中培养软骨细胞可能是研究溶酶体贮积病中导致骨骼异常的软骨生物学的一种有用方法。