Yuko Hamada's research while affiliated with Kitasato University and other places

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Publications (6)


Changes in CD4 T cell subsets (Th-1, Th-2) in skin lesions of patients with atopic dermatitis
  • Article

August 1993

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10 Reads

Journal of Dermatological Science

Takao Fujimura

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Akira Fujioka

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Yuko Hamada

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[...]

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Shigeo Nishiyama
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Pigment Production in Murine Melanoma Cells Is Regulated by Tyrosinase, Tyrosinase-Related Protein 1 (TRP1), DOPAchrome Tautomerase (TRP2), and a Melanogenic Inhibitor

March 1993

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26 Reads

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116 Citations

Journal of Investigative Dermatology

Using antibodies that recognize either tyrosinase, tyrosinase-related protein-1 (TRP1), or tyrosinase-related protein-2 (TRP2, DOPAchrome tautomerase), the quantities of those melanogenic enzymes were analyzed in five melanoma cell lines that possess various degrees of melanin production. All cells except JB/MS-W increased melanin production four to 30 times after 4 d of melanocyte-stimulating hormone (MSH) treatment. Melanin production by JB/MS-W cells was always under background, with or without MSH treatment. There was a positive correlation between quantities and synthetic rates of those melanogenic enzymes and their melanin formation or DOPAchrome tautomerase activities. The activity of a heat-resistant melanogenic inhibitory factor was also analyzed. The results showed, surprisingly, that pigmented cells showed higher levels of melanogenic inhibitors activity. Tyrosinase activity was increased dramatically whereas the level of melanogenic inhibitor was remarkably decreased following MSH treatment. Interestingly, melanogenic inhibitor derived from JB/MS-W cells suppressed not only tyrosinase but also DOPAchrome tautomerase, another enzyme functional in melanin production. These results clearly suggest that melanin production is regulated by a subtle balance between the activities of these enzymes and other factors such as the melanogenic inhibitor.


Citations (1)


... China as the other 2 key enzymes in the melanogenesis pathway, the gene expression of TRP-1 and TRP-2 is also critical in promoting melanin synthesis. [15][16][17][18] Therefore, to inhibit melanin production by inhibiting TYR or intermediates of melanogenesis in cells is the most common mechanism of cosmetics for skin whitening at present. 13,19 In this study, we demonstrated the whitening effects of SAA and SAB using a cell co-culture system to assess the impact on melanocyte activity, melanin and melanin-related enzymes, and their gene expression. ...

Reference:

Potential Beneficial Effects of Salvianic Acid A and Salvianolic Acid B in Skin Whitening
Pigment Production in Murine Melanoma Cells Is Regulated by Tyrosinase, Tyrosinase-Related Protein 1 (TRP1), DOPAchrome Tautomerase (TRP2), and a Melanogenic Inhibitor
  • Citing Article
  • March 1993

Journal of Investigative Dermatology