首页> 外文期刊>FEBS Letters >The involvement of p38 mitogen‐activated protein kinase in the α‐melanocyte stimulating hormone (α‐MSH)‐induced melanogenic and anti‐proliferative effects in B16 murine melanoma cells
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The involvement of p38 mitogen‐activated protein kinase in the α‐melanocyte stimulating hormone (α‐MSH)‐induced melanogenic and anti‐proliferative effects in B16 murine melanoma cells

机译:p38丝裂原激活的蛋白激酶参与了B16鼠黑色素瘤细胞中α-黑素细胞刺激激素(α-MSH)诱导的黑素生成和抗增殖作用

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>Activation of p38 or p44/42 mitogen-activated protein (MAP) kinases has been shown to trigger differentiation in a number of cell types. The present study has investigated the roles of these kinases in the α-melanocyte stimulating hormone (α-MSH)-induced melanogenic and proliferative responses in B16 melanoma cells. Treatment of cells with α-MSH led to the time-dependent phosphorylation of both p38 and p44/42 MAP kinases. However, only inhibition of p38 MAP kinase activity with SB 203580 blocked both the α-MSH-induced melanogenic and anti-proliferative effects. It therefore appears that activation of the p38 pathway can promote melanogenesis and inhibit growth of B16 melanoma cells.
机译:p38或p44 / 42丝裂原激活的蛋白(MAP)激酶的激活已显示可触发多种细胞类型的分化。本研究已经研究了这些激酶在α-黑素细胞刺激激素(α-MSH)诱导的B16黑素瘤细胞中的黑色素生成和增殖反应中的作用。用α-MSH处理细胞会导致p38和p44 / 42 MAP激酶的时间依赖性磷酸化。但是,只有用SB 203580抑制p38 MAP激酶的活性才能阻断α-MSH诱导的黑色素生成和抗增殖作用。因此,看来p38途径的激活可以促进黑色素生成并抑制B16黑色素瘤细胞的生长。

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