Danks D M, Cartwright E, Stevens B J, Townley R R
Science. 1973 Mar 16;179(4078):1140-2. doi: 10.1126/science.179.4078.1140.
Duodenal mucosa obtained from two patients with Menkes' syndrome contained abnormally large amounts of copper. The defect in copper absorption in this disease must lie in the process of intracellular handling or of transport across the serosal cell membrane. Fibroblastic cells cultured from the skin of patients and of heterozygous females show intense metachromasia in primary culture which disappears in subculture. These cells may be useful for the study of copper transport in vitro and for the identification of heterozygotes in affected families.
从两名门克斯综合征患者获取的十二指肠黏膜含铜量异常高。该疾病中铜吸收的缺陷必定存在于细胞内处理过程或跨浆膜细胞膜转运过程中。从患者及杂合子女性皮肤培养的成纤维细胞在原代培养中显示出强烈的异染性,传代培养时则消失。这些细胞可能有助于体外铜转运的研究以及患病家族中杂合子的鉴定。