巨噬细胞迁移抑制因子(MIF)家族在器官纤维化中的多重作用。

IF 5 2区 生物学 Q2 CELL BIOLOGY
Lea Herkens, Patrick Droste, Peter Boor
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引用次数: 0

摘要

巨噬细胞迁移抑制因子(MIF)家族由结构上同源的蛋白MIF、D-dopachrome tautomerase (D- dt)和D- dt样蛋白(D- DTL)组成。虽然MIF是描述得最好的成员,但对D-DT知之甚少,对D- dtl知之甚少。在这里,我们提供了这些蛋白质的结构,相似性和生物学功能的概述。根据疾病类型、受累器官、细胞类型和疾病分期的不同,MIF和D-DT对多种疾病既有保护作用,也有加重作用。鉴于许多慢性疾病的病理结果是纤维化,我们在此讨论这些蛋白在器官纤维化中的作用,特别是肾、肝、心、肺和皮肤。我们讨论了这些蛋白的各种作用,表明MIF可能在不同器官中具有促纤维化和抗纤维化作用。迄今为止,D-DT已被证明仅具有抗纤维化作用。我们解决了潜在的翻译考虑,并提出了未来的研究途径,以更好地了解mif家族在器官纤维化中的参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The multifaced role of the macrophage-migration-inhibitory-factor (MIF)-family in organ fibrosis.

The macrophage-migration-inhibitory-factor (MIF)-family consists of the structurally homologous proteins MIF, D-dopachrome tautomerase (D-DT), and D-DT like (D- DTL). While MIF is the most well-described member, much less is known about D- DT, and very little about D-DTL. Here, we provide an overview of the structure, similarities, and biological functions of these proteins. MIF and D-DT can have both protective and aggravating effects on various diseases depending on the disease type, involved organ, cell type, and disease stage. Given that the pathological consequence of many chronic diseases is fibrosis, we here discuss the role of these proteins in organ fibrosis, particularly of the kidney, liver, heart, lung, and skin. We discuss the various roles of these proteins, suggesting that MIF might have pro- and antifibrotic roles in different organs. To date, D-DT has been shown to have only antifibrotic roles. We tackle potential translational considerations and propose future research avenues to better understand the involvement of MIF-family in organ fibrosis.

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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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