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人脐带血间充质干细胞条件培养基通过促进小眼畸形相关转录因子(MITF)的蛋白酶体降解来抑制黑色素生成。

Conditioned Media from Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells Inhibits Melanogenesis by Promoting Proteasomal Degradation of MITF.

作者信息

Kim Eun Sung, Jeon Hong Bae, Lim Hoon, Shin Ji Hyun, Park So Jung, Jo Yoon Kyung, Oh Wonil, Yang Yoon Sun, Cho Dong-Hyung, Kim Ju-Yeon

机构信息

Graduate School of East-West Medical Science, Kyung Hee University, Yongin-si, Gyeonggi-do, Republic of Korea.

Biomedical Research Institute, MEDIPOST Co., Ltd., Seongnam-si, Gyeonggi-do, Republic of Korea.

出版信息

PLoS One. 2015 May 29;10(5):e0128078. doi: 10.1371/journal.pone.0128078. eCollection 2015.

Abstract

Human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs) secrete various beneficial molecules, which have anti-apoptotic activity and cell proliferation. However, the effect of hUCB-MSCs in melanogenesis is largely unclear. In this study, we show that conditioned media (CM) derived from hUCB-MSCs inhibit melanogenesis by regulating microphthalmia-associated transcription factor (MITF) expression via the ERK signalling pathway. Treatment of hUCB-MSC-CM strongly inhibited the alpha-melanocyte stimulating hormone-induced hyperpigmentation in melanoma cells as well as melanocytes. Treatment of hUCB-MSC-CM induced ERK1/2 activation in melanocytes. In addition, inhibition of ERK1/2 suppressed the anti-pigmentation activity of the hUCB-MSC-CM in melanocytes and in vitro artificial skin models. We also found that the expression of MITF was appreciably diminished while expression of phosphorylated MITF, which leads to its proteasomal degradation, was increased in cells treated with hUCB-MSC-CM. These results suggested that hUCB-MSC-CM significantly suppresses melanin synthesis via MITF degradation by the ERK pathway activation.

摘要

人脐带血间充质干细胞(hUCB-MSCs)分泌多种有益分子,这些分子具有抗凋亡活性和促进细胞增殖的作用。然而,hUCB-MSCs在黑色素生成中的作用在很大程度上尚不清楚。在本研究中,我们发现hUCB-MSCs来源的条件培养基(CM)通过ERK信号通路调节小眼相关转录因子(MITF)的表达来抑制黑色素生成。hUCB-MSC-CM处理强烈抑制了α-黑素细胞刺激素诱导的黑色素瘤细胞以及黑素细胞中的色素沉着过度。hUCB-MSC-CM处理诱导了黑素细胞中ERK1/2的激活。此外,抑制ERK1/2可抑制hUCB-MSC-CM在黑素细胞和体外人工皮肤模型中的抗色素沉着活性。我们还发现,在用hUCB-MSC-CM处理的细胞中,MITF的表达明显减少,而导致其蛋白酶体降解的磷酸化MITF的表达增加。这些结果表明,hUCB-MSC-CM通过ERK途径激活导致MITF降解,从而显著抑制黑色素合成。

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