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2024 年卡帕三角洲青年研究员奖:利用发育学的见解改善成人生物修复: hedgehog 信号作为腱-骨结合部纤维软骨形成的主调控因子。

The 2024 Kappa Delta Young Investigator Award: Leveraging Insights From Development to Improve Adult Repair: Hedgehog Signaling as a Master Regulator of Enthesis Fibrocartilage Formation.

机构信息

From the Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA (Dr. Dyment, Dr. Kamalitdinov, and Dr. Kuntz), and the Department of Bioengineering, University of Pennsylvania, Philadelphia, PA (Dr. Dyment and Dr. Kamalitdinov).

出版信息

J Am Acad Orthop Surg. 2024 Dec 1;32(23):1074-1086. doi: 10.5435/JAAOS-D-24-00996.

Abstract

The work in this article summarizes findings from our group on key biochemical cues that govern the formation and repair of tendons and ligaments. Specifically, we summarize the journey that started with a serendipitous discovery that is now being translated into novel therapies to improve tendon-to-bone repair outcomes. This journey began with the discovery that the Hedgehog (Hh) signaling pathway was expressed within the enthesis during development and that its primary role was to promote fibrocartilage production and maturation. Next, we developed an anterior cruciate ligament reconstruction model in novel transgenic mice that allowed us to discover that the Hh pathway promotes fibrocartilaginous tendon-to-bone attachments during the integration process. In addition, we established that the coordinated stages of zonal tendon-to-bone integration after anterior cruciate ligament reconstruction were comparable with the stages required for enthesis formation during development. Now that we have demonstrated that the Hh pathway is a potent therapeutic target, we are currently advancing these findings to develop drug delivery systems to improve tendon-to-bone repair. Ultimately, our group aims to establish key mechanisms that govern tendon and ligament formation that can be leveraged for novel regenerative therapies to improve clinical care.

摘要

本文的工作总结了我们小组在控制肌腱和韧带形成和修复的关键生化线索方面的发现。具体来说,我们总结了从一个偶然发现开始的历程,该发现现在正在被转化为改善肌腱-骨修复效果的新疗法。这一历程始于发现 Hedgehog(Hh)信号通路在发育过程中存在于附着处,其主要作用是促进纤维软骨的产生和成熟。接下来,我们在新型转基因小鼠中开发了前交叉韧带重建模型,使我们能够发现 Hh 通路在整合过程中促进纤维软骨性肌腱-骨附着。此外,我们确定了前交叉韧带重建后区域性肌腱-骨整合的协调阶段与发育过程中附着形成所需的阶段相当。既然我们已经证明 Hh 通路是一个有效的治疗靶点,我们目前正在推进这些发现,以开发药物输送系统来改善肌腱-骨修复。最终,我们小组的目标是建立控制肌腱和韧带形成的关键机制,这些机制可以被用于新的再生治疗方法,以改善临床护理。

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