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肺纤维化中的小窝蛋白-1信号传导

Caveolin-1 signaling in lung fibrosis.

作者信息

Tourkina Elena, Hoffman Stanley

机构信息

Division of Rheumatology and Immunology, Department of Medicine, Medical University of South Carolina, 96 Jonathan Lucas Street, Suite 912, MSC 637, Charleston, SC 29425, USA.

出版信息

Open Rheumatol J. 2012;6:116-22. doi: 10.2174/1874312901206010116. Epub 2012 Jun 15.

DOI:10.2174/1874312901206010116
PMID:22802909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3396359/
Abstract

Caveolin-1 is a master regulator of several signaling cascades because it is able to bind to and thereby inhibit members of a variety of kinase families. While associated with caveolae and involved in their generation, caveolin-1 is also present at other sites. A variety of studies have suggested that caveolin-1 may be a useful therapeutic target in fibrotic diseases of the lung and other tissues because in these diseases a low level of caveolin-1 expression is associated with a high level of collagen expression and fibrosis. Reduced caveolin-1 expression is observed not only in the fibroblasts that secrete collagen, but also in epithelial cells and monocytes. This is intriguing because both epithelial cells and monocytes have been suggested to be precursors of fibroblasts. Likely downstream effects of loss of caveolin-1 in fibrosis include activation of TGF-β signaling and upregulation of CXCR4 in monocytes resulting in their enhanced migration into damaged tissue where its ligand CXCL12 is produced. Finally, it may be possible to target caveolin-1 in fibrotic diseases without the use of gene therapy. A caveolin-1 peptide (caveolin-1 scaffolding domain) has been identified that retains the function of the full-length molecule to inhibit kinases and that can be modified by addition of the Antennapedia internalization sequence to allow it to enter cells both in vitro and in vivo.

摘要

小窝蛋白-1是多种信号级联反应的主要调节因子,因为它能够结合并抑制多种激酶家族的成员。虽然小窝蛋白-1与小窝相关并参与其形成,但它也存在于其他部位。多项研究表明,小窝蛋白-1可能是治疗肺部和其他组织纤维化疾病的一个有用的治疗靶点,因为在这些疾病中,小窝蛋白-1的低表达水平与高水平的胶原蛋白表达和纤维化相关。不仅在分泌胶原蛋白的成纤维细胞中观察到小窝蛋白-1表达降低,在上皮细胞和单核细胞中也观察到了这种情况。这很有趣,因为上皮细胞和单核细胞都被认为是成纤维细胞的前体。小窝蛋白-1缺失在纤维化中的可能下游效应包括TGF-β信号的激活和单核细胞中CXCR4的上调,导致它们向产生其配体CXCL12的受损组织中迁移增加。最后,在不使用基因治疗的情况下,针对纤维化疾病中的小窝蛋白-1可能是可行的。已经鉴定出一种小窝蛋白-1肽(小窝蛋白-1支架结构域),它保留了全长分子抑制激酶的功能,并且可以通过添加触角足内化序列进行修饰,使其能够在体外和体内进入细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6690/3396359/56755ac07f6d/TORJ-6-116_F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6690/3396359/c2d953d30cff/TORJ-6-116_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6690/3396359/56755ac07f6d/TORJ-6-116_F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6690/3396359/c2d953d30cff/TORJ-6-116_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6690/3396359/56755ac07f6d/TORJ-6-116_F2.jpg

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Fibrogenesis Tissue Repair. 2011 Jul 1;4(1):15. doi: 10.1186/1755-1536-4-15.
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JCI Insight. 2020 Oct 2;5(19):137969. doi: 10.1172/jci.insight.137969.
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Klotho antagonizes pulmonary fibrosis through suppressing pulmonary fibroblasts activation, migration, and extracellular matrix production: a therapeutic implication for idiopathic pulmonary fibrosis.Klotho 通过抑制肺成纤维细胞的激活、迁移和细胞外基质的产生来拮抗肺纤维化:对特发性肺纤维化的治疗意义。
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