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Merck
CN
  • ARP101 inhibits α-MSH-stimulated melanogenesis by regulation of autophagy in melanocytes.

ARP101 inhibits α-MSH-stimulated melanogenesis by regulation of autophagy in melanocytes.

FEBS letters (2013-11-06)
Eun Sung Kim, Yoon Kyung Jo, So Jung Park, Huikyoung Chang, Ji Hyun Shin, Eun Sun Choi, Jun Bum Kim, Su Hyeon Seok, Jae-Sung Kim, Jeong Su Oh, Myoung-Hwan Kim, Eunjoo H Lee, Dong-Hyung Cho
摘要

Autophagy is a cooperative process between autophagosomes and lysosomes that degrades cellular organelles. Although autophagy regulates the turnover of cellular components, its role in melanogenesis is not clearly established. Previously, we reported that ARP101 induces autophagy in various cancer cells. Here, we show that ARP101 inhibits melanogenesis by regulation of autophagy. ARP101 inhibited α-MSH-stimulated melanin synthesis and suppressed the expression of tyrosinase and TRP1 in immortalized mouse melanocytes. ARP101 also induced autophagy in melanocytes. Knockdown of ATG5 reduced both anti-melanogenic activity and autophagy mediated by ARP101 in α-MSH treated melanocytes. Electron microscopy analysis further revealed that autophagosomes engulf melanin or melanosome in α-MSH and ARP101-treated cells. Collectively, our results suggest that ARP101 inhibits α-MSH-stimulated melanogenesis through the activation of autophagy in melanocytes.

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酪氨酸酶 来源于蘑菇, lyophilized powder, ≥1000 unit/mg solid
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抗肌动蛋白抗体,克隆C4, ascites fluid, clone C4, Chemicon®