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1型神经纤维瘤病(NF 1)患者培养的表皮黑素细胞中黑素生成增加。

Increased melanogenesis in cultured epidermal melanocytes from patients with neurofibromatosis 1 (NF 1).

作者信息

Kaufmann D, Wiandt S, Veser J, Krone W

机构信息

Abteilung Humangenetik, Universität, Ulm, Federal Republic of Germany.

出版信息

Hum Genet. 1991 Jun;87(2):144-50. doi: 10.1007/BF00204170.

Abstract

Melanocyte cultures from the normally pigmented skin of patients with neurofibromatosis 1 (NF 1) have a higher melanin content than those from the skin of healthy donors. An additional increase in the amount of melanin per cell was found in 5 out of 6 lines of melanocytes derived from café au lait macules of NF 1 patients. Omission of the tumor promoter phorbol-12-myristate-13-acetate from the culture medium brings about a comparable increase in the melanin content in all three kinds of melanocyte cultures. Cultures of NF 1 melanocytes show a higher tyrosine hydroxylase activity than those of control melanocytes, and incorporate larger amounts of dihydroxyphenylalanine than the latter. We conclude that melanogenesis in epidermis melanocytes is affected by defective alleles of the NF 1 gene. Our findings do not contradict the hypothesis that the defect underlying NF 1 impairs the inhibition of a wild-type RAS oncogene by interfering with the GTPase-activating function of the NF 1 gene product.

摘要

1型神经纤维瘤病(NF 1)患者正常色素沉着皮肤的黑素细胞培养物中的黑色素含量高于健康供体皮肤的黑素细胞培养物。在源自NF 1患者咖啡斑的6株黑素细胞系中,有5株发现每细胞黑色素量额外增加。从培养基中省略肿瘤启动子佛波醇-12-肉豆蔻酸酯-13-乙酸酯会导致所有三种黑素细胞培养物中的黑色素含量出现类似增加。NF 1黑素细胞培养物显示出比对照黑素细胞更高的酪氨酸羟化酶活性,并且比后者掺入更多的二羟基苯丙氨酸。我们得出结论,表皮黑素细胞中的黑色素生成受NF 1基因缺陷等位基因的影响。我们的发现与以下假设并不矛盾,即NF 1潜在的缺陷通过干扰NF 1基因产物的GTP酶激活功能来损害野生型RAS癌基因的抑制作用。

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