Danes B S, Scott J E, Bearn A G
J Exp Med. 1970 Oct 1;132(4):765-74. doi: 10.1084/jem.132.4.765.
Staining with Alcian blue in various concentrations of magnesium chloride (alcianophilia) has been found to be a useful supplement to metachromatic staining to detect increased cellular concentrations of glycosaminoglycans (mucopolysaccharides). In many instances alcianophilia at 0.3 M MgCl(2) is more specific than metachromasia and does not give "false positives" sometimes found in normal individuals and in those with cystic fibrosis, Gaucher's disease, familial amaurotic idiocy, and pseudoxanthoma elasticum. On the other hand, it gives a "false negative" reaction in the Sanfilippo syndrome (perhaps because the characteristically elevated glycosaminoglycan in this disease, heparan sulfate, is not synthesized by cultured skin fibroblasts), and in the Marfan syndrome. It detects the Maroteaux-Lamy syndrome, which metachromasia does not. The "false positives" given by metachromasia in all six families studied thus far are genuine, reproducible reactions that can be traced through at least three generations of normal individuals within a family. There is therefore, in these families, a genetic factor that causes such metachromasia, but it is not increased glycosaminoglycan concentration.
在不同浓度氯化镁中用阿尔辛蓝染色(嗜阿尔辛蓝性)已被发现是对异染性染色的一种有用补充,用于检测细胞中糖胺聚糖(粘多糖)浓度的增加。在许多情况下,0.3M氯化镁时的嗜阿尔辛蓝性比异染性更具特异性,并且不会出现正常个体以及患有囊性纤维化、高雪氏病、家族性黑蒙性白痴和弹性假黄瘤的患者中有时出现的“假阳性”。另一方面,它在Sanfilippo综合征(可能是因为该疾病中特征性升高的糖胺聚糖硫酸乙酰肝素不是由培养的皮肤成纤维细胞合成的)和马凡综合征中会给出“假阴性”反应。它能检测出马罗托-拉米综合征,而异染性染色则不能。到目前为止,在所研究的所有六个家族中异染性染色给出的“假阳性”都是真实的、可重复的反应,在一个家族中至少可以追溯到三代正常个体。因此,在这些家族中,存在一个导致这种异染性染色的遗传因素,但不是糖胺聚糖浓度增加。