4.2 Article

Transcriptomic, Proteomic, and Morphologic Characterization of Healing in Volumetric Muscle Loss

期刊

TISSUE ENGINEERING PART A
卷 28, 期 23-24, 页码 941-957

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/ten.tea.2022.0113

关键词

volumetric muscle loss; tissue engineering; regenerative medicine; wound healing

资金

  1. Defense Advanced Research Projects Agency - U.S. Department of the Interior, Interior Business Center
  2. [D20AC00002]

向作者/读者索取更多资源

The comprehensive analysis of wound healing process in a novel canine model of VML, compared with a nine-patient cohort of combat-associated VML, provides a translational framework and model system for future studies investigating novel therapies for human VML.
Skeletal muscle has a robust, inherent ability to regenerate in response to injury from acute to chronic. In severe trauma, however, complete regeneration is not possible, resulting in a permanent loss of skeletal muscle tissue referred to as volumetric muscle loss (VML). There are few consistently reliable therapeutic or surgical options to address VML. A major limitation in investigation of possible therapies is the absence of a well-characterized large animal model. In this study, we present results of a comprehensive transcriptomic, proteomic, and morphologic characterization of wound healing following VML in a novel canine model of VML which we compare to a nine-patient cohort of combat-associated VML. The canine model is translationally relevant as it provides both a regional (spatial) and temporal map of the wound healing processes that occur in human VML. Collectively, these data show the spatiotemporal transcriptomic, proteomic, and morphologic properties of canine VML healing as a framework and model system applicable to future studies investigating novel therapies for human VML. Impact StatementThe spatiotemporal transcriptomic, proteomic, and morphologic properties of canine volumetric muscle loss (VML) healing is a translational framework and model system applicable to future studies investigating novel therapies for human VML.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据