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肝 X 受体在人黑素细胞中的表达,它在白癜风发病机制中起作用吗?

Liver X receptor expression in human melanocytes, does it have a role in the pathogenesis of vitiligo?

出版信息

Exp Dermatol. 2010 Jan;19(1):62-4. doi: 10.1111/j.1600-0625.2009.00940.x. Epub 2009 Jul 23.

DOI:10.1111/j.1600-0625.2009.00940.x
PMID:19645823
Abstract

Vitiligo is a common, non-contagious disorder. The basic pathogenesis of vitiligo generally, or for any of the putative subsets of vitiligo, remains unknown. The liver X receptors (LXRs), LXR-alpha and LXR-beta are members of the nuclear hormone receptor superfamily of ligand-activated transcription factors. Important genes involved in regulation of melanocytes are target genes of LXRs; it can be speculated that LXRs might be playing an important role in pathogenesis of pigmentary disorders. We have demonstrated in this study that there is expression of LXR-alpha/beta by human melanocytes at both transcriptional and translational levels. Our present data also revealed that the expression of LXR-alpha at both mRNA and protein level was significantly higher in perilesional skin as compared to the normal skin of vitiligo patient.

摘要

白癜风是一种常见的非传染性疾病。白癜风的基本发病机制一般或任何假定的白癜风亚群仍然未知。肝 X 受体 (LXRs),LXR-α和 LXR-β是配体激活转录因子的核激素受体超家族的成员。参与黑素细胞调节的重要基因是 LXRs 的靶基因;可以推测,LXRs 可能在色素障碍的发病机制中发挥重要作用。我们在这项研究中证明了人类黑素细胞在转录和翻译水平上均有 LXR-α/β的表达。我们目前的数据还显示,与白癜风患者正常皮肤相比,白癜风皮损皮肤中 LXR-α 的 mRNA 和蛋白水平表达显著升高。

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Liver X receptor expression in human melanocytes, does it have a role in the pathogenesis of vitiligo?肝 X 受体在人黑素细胞中的表达,它在白癜风发病机制中起作用吗?
Exp Dermatol. 2010 Jan;19(1):62-4. doi: 10.1111/j.1600-0625.2009.00940.x. Epub 2009 Jul 23.
2
Altered levels of LXR-α: crucial implications in the pathogenesis of vitiligo.LXR-α 水平的改变:在白癜风发病机制中的关键意义。
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MicroRNA-155 is Dysregulated in the Skin of Patients with Vitiligo and Inhibits Melanogenesis-associated Genes in Melanocytes and Keratinocytes.微小RNA-155在白癜风患者皮肤中表达失调,并抑制黑素细胞和角质形成细胞中与黑素生成相关的基因。
Acta Derm Venereol. 2016 Aug 23;96(6):742-7. doi: 10.2340/00015555-2394.

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Beauvericin inhibits melanogenesis by regulating cAMP/PKA/CREB and LXR-α/p38 MAPK-mediated pathways.
beauvericin 通过调节 cAMP/PKA/CREB 和 LXR-α/p38 MAPK 介导的途径抑制黑色素生成。
Sci Rep. 2018 Oct 8;8(1):14958. doi: 10.1038/s41598-018-33352-8.
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Re-appraisal of Keratinocytes' Role in Vitiligo Pathogenesis.角质形成细胞在白癜风发病机制中的作用再评估。
Indian J Dermatol. 2018 May-Jun;63(3):231-240. doi: 10.4103/ijd.IJD_520_17.
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Liver X Receptor-α polymorphisms (rs11039155 and rs2279238) are associated with susceptibility to vitiligo.肝脏X受体α基因多态性(rs11039155和rs2279238)与白癜风易感性相关。
Meta Gene. 2016 Feb 10;8:33-6. doi: 10.1016/j.mgene.2016.02.001. eCollection 2016 Jun.
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Liver X receptor activation induces apoptosis of melanoma cell through caspase pathway.肝 X 受体激活通过半胱天冬酶途径诱导黑素瘤细胞凋亡。
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Nuclear hormone receptor functions in keratinocyte and melanocyte homeostasis, epidermal carcinogenesis and melanomagenesis.核激素受体在角质形成细胞和黑素细胞的稳态、表皮癌发生和黑色素瘤发生中发挥作用。
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