首页> 美国卫生研究院文献>Cell Regulation >Identification and characterization of a novel collagenase in Xenopus laevis: possible roles during frog development.
【2h】

Identification and characterization of a novel collagenase in Xenopus laevis: possible roles during frog development.

机译:鉴定和表征非洲爪蟾中的新型胶原酶:在青蛙发育过程中的可能作用。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Matrix metalloproteinases (MMPs) participate in extracellular matrix remodeling and degradation and have been implicated in playing important roles during organ development and pathological processes. Although it has been hypothesized for > 30 years that collagenase activities are responsible for collagen degradation during tadpole tail resorption, none of the previously cloned amphibian MMPs have been biochemically demonstrated to be collagenases. Here, we report a novel matrix metalloproteinase gene from metamorphosing Xenopus laevis tadpoles. In vitro biochemical studies demonstrate that this Xenopus enzyme is an interstitial collagenase and has an essentially identical enzymatic activity toward a collagen substrate as the human interstitial collagenase. Sequence comparison of this enzyme to other known MMPs suggests that the Xenopus collagenase is not a homologue of any known collagenases but instead represents a novel collagenase, Xenopus collagenase-4 (xCol4, MMP-18). Interestingly, during development, xCol4 is highly expressed only transiently in whole animals, at approximately the time when tadpole feeding begins, suggesting a role during the maturation of the digestive tract. More importantly, during metamorphosis, xCol4 is regulated in a tissue-dependent manner. High levels of its mRNA are present as the tadpole tail resorbs. Similarly, its expression is elevated during hindlimb morphogenesis and intestinal remodeling. In addition, when premetamorphic tadpoles are treated with thyroid hormone, the causative agent of metamorphosis, xCol4 expression is induced in the tail. These results suggest that xCol4 may facilitate larval tissue degeneration and adult organogenesis during amphibian metamorphosis.
机译:基质金属蛋白酶(MMP)参与细胞外基质的重塑和降解,并参与器官发育和病理过程中的重要作用。尽管已经有超过30年的假说,认为胶原酶的活性是t尾部吸收过程中胶原降解的原因,但是以前克隆的两栖MMP都没有被生化证明是胶原酶。在这里,我们报告从变形非洲爪蟾t的新型基质金属蛋白酶基因。体外生化研究表明,这种非洲爪蟾酶是一种间质胶原酶,对胶原蛋白底物的酶活性与人间质胶原酶基本相同。该酶与其他已知MMP的序列比较表明,非洲爪蟾胶原酶不是任何已知胶原酶的同源物,而是代表一种新型胶原酶,非洲爪蟾胶原酶-4(xCol4,MMP-18)。有趣的是,在发育过程中,xCol4仅在whole开始喂养的大约整个时间在整个动物中高表达,这暗示着在消化道成熟过程中的作用。更重要的是,在变态过程中,xCol4以组织依赖性方式被调控。随着mRNA尾部吸收,其mRNA含量较高。同样,其表达在后肢形态发生和肠重构过程中也升高。此外,当用甲状腺激素(变态的病因)治疗变态前的t时,会在尾巴中诱导出xCol4表达。这些结果表明xCol4可能促进两栖动物变态期间幼虫组织变性和成年器官发生。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号