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原弹性蛋白的交联、自缔合和成熟的不同步骤是弹性纤维形成所必需的。

Distinct steps of cross-linking, self-association, and maturation of tropoelastin are necessary for elastic fiber formation.

作者信息

Sato Fumiaki, Wachi Hiroshi, Ishida Marie, Nonaka Risa, Onoue Satoshi, Urban Zsolt, Starcher Barry C, Seyama Yoshiyuki

机构信息

Department of Clinical Chemistry, Hoshi University School of Pharmacy and Pharmaceutical Sciences, 2-4-41 Ebara, Shinagawa-ku, Tokyo 142-8501, Japan.

出版信息

J Mol Biol. 2007 Jun 8;369(3):841-51. doi: 10.1016/j.jmb.2007.03.060. Epub 2007 Apr 4.

Abstract

Elastic fibers play an important role in the characteristic resilience of many tissues. The assembly of tropoelastin into a fibrillar matrix is a complex stepwise process and the deposition and cross-linking of tropoelastin are believed to be key steps of elastic fiber formation. However, the detailed mechanisms of elastic fiber assembly have not been defined yet. Here, we demonstrate the relationship between deposition and the cross-linking/maturation of tropoelastin. Our data show that a C-terminal half-fragment of tropoelastin encoded by exons 16-36 (BH) is deposited onto microfibrils, yet we detect very limited amounts of the cross-linking amino acid, desmosine, an indicator of maturation, whereas the N-terminal half-fragment encoded by exons 2-15 (FH) was deficient for both deposition and cross-linking, suggesting that elastic fiber formation requires full-length tropoelastin molecules. A series of experiments using mutant BH fragments, lacking either exon 16 or 30, or a deletion of both exons showed that self-association of tropoelastin polypeptides was an early step in elastic fiber assembly. Immunofluorescence and Western blot assay showed that the treatment of cell culture medium or conditioned medium with beta-aminopropionitrile to inhibit cross-linking, prevented both the deposition and polymerization of tropoelastin. In conclusion, our present results support the view that self-association and oxidation by lysyl oxidase precedes tropoelastin deposition onto microfibrils and the entire molecule of tropoelastin is required for this following maturation process.

摘要

弹性纤维在许多组织特有的弹性中发挥着重要作用。原弹性蛋白组装成纤维状基质是一个复杂的逐步过程,原弹性蛋白的沉积和交联被认为是弹性纤维形成的关键步骤。然而,弹性纤维组装的详细机制尚未明确。在此,我们阐述了原弹性蛋白沉积与交联/成熟之间的关系。我们的数据表明,由外显子16 - 36编码的原弹性蛋白C端半片段(BH)沉积在微原纤维上,但我们检测到交联氨基酸锁链素(成熟的一个指标)的量非常有限,而由外显子2 - 15编码的N端半片段(FH)在沉积和交联方面均不足,这表明弹性纤维的形成需要全长的原弹性蛋白分子。一系列使用缺失外显子16或30或两个外显子均缺失的突变BH片段的实验表明,原弹性蛋白多肽的自我缔合是弹性纤维组装的早期步骤。免疫荧光和蛋白质印迹分析表明,用β-氨基丙腈处理细胞培养基或条件培养基以抑制交联,会阻止原弹性蛋白的沉积和聚合。总之,我们目前的结果支持这样一种观点,即原弹性蛋白在微原纤维上的沉积之前发生自我缔合和赖氨酰氧化酶介导的氧化作用,并且整个原弹性蛋白分子对于随后的成熟过程是必需的。

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