关于白癜风的最新假说:大多数白癜风的发病机制可归因于锌-α2糖蛋白的缺乏。

ISRN Dermatology Pub Date : 2012-01-01 Epub Date: 2012-06-19 DOI:10.5402/2012/405268
Nooshin Bagherani
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引用次数: 11

摘要

锌α2-糖蛋白(Zinc-α2-glycoprotein, ZAG)是最近发现的一种脂肪因子,位于染色体7q22.1上。它是一种多学科蛋白质,在各种体液中分泌。ZAG在脂肪分解、调节代谢、细胞增殖和分化、调节黑色素合成、细胞粘附、免疫调节等方面发挥作用。白癜风是最常见的脱色性皮肤疾病,其特征是皮肤和头发的获得性、进行性和限制性白变。它通常开始于童年或青年期。这种疾病的发病机制尚不确定,但它似乎依赖于遗传、免疫和神经因素的相互作用。我们首次指出了ZAG与白癜风之间的可能联系。在这里,我从不同的角度描述了这种联系。通过证实这种关联,将在治疗这种普遍的使人衰弱的疾病方面取得令人惊讶的进展。
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The Newest Hypothesis about Vitiligo: Most of the Suggested Pathogeneses of Vitiligo Can Be Attributed to Lack of One Factor, Zinc-α2-Glycoprotein.

Zinc-α2-glycoprotein (ZAG) is a recently identified adipokine, assigned to the chromosome 7q22.1. It is a multidisciplinary protein, which is secreted in various body fluids. The ZAG plays roles in lipolysis, regulation of metabolism, cell proliferation and differentiation, regulation of melanin synthesis, cell adhesion, immunoregulation, and so forth. Vitiligo is the most common depigmenting skin disorder, characterized by acquired, progressive, and circumscribed amelanosis of the skin and hair. It commonly begins in childhood or young adulthood. The pathogenesis of this disorder is uncertain, but it appears to be dependent on the interaction of genetic, immunological, and neurological factors. For the first time, we pointed the probable association between ZAG and vitiligo. Herein, I have described this association in different views. By confirming this association, a surprising progression will occur in the treatment of this prevalent debilitating disease.

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