Carbonell-M Belfran, Zapata Cardona Juliana, Delgado Jean Paul
Grupo de Genética, Regeneración y Cáncer, Universidad de Antioquia, Sede de Investigación Universitaria, Medellín, Colombia.
Departamento de Estudios Básicos Integrados, Facultad de Odontología, Universidad de Antioquia, Medellín, Colombia.
Front Cell Dev Biol. 2022 Aug 26;10:921520. doi: 10.3389/fcell.2022.921520. eCollection 2022.
Reactive oxygen species (ROS) represent molecules of great interest in the field of regenerative biology since several animal models require their production to promote and favor tissue, organ, and appendage regeneration. Recently, it has been shown that the production of ROS such as hydrogen peroxide (HO) is required for tail regeneration in . However, to date, it is unknown whether ROS production is necessary for limb regeneration in this animal model. Methods: forelimbs of juvenile animals were amputated proximally and the dynamics of ROS production was determined using 2'7- dichlorofluorescein diacetate (DCFDA) during the regeneration process. Inhibition of ROS production was performed using the NADPH oxidase inhibitor apocynin. Subsequently, a rescue assay was performed using exogenous hydrogen peroxide (HO). The effect of these treatments on the size and skeletal structures of the regenerated limb was evaluated by staining with alcian blue and alizarin red, as well as the effect on blastema formation, cell proliferation, immune cell recruitment, and expression of genes related to proximal-distal identity. Results: our results show that inhibition of post-amputation limb ROS production in the salamander model results in the regeneration of a miniature limb with a significant reduction in the size of skeletal elements such as the ulna, radius, and overall autopod. Additionally, other effects such as decrease in the number of carpals, defective joint morphology, and failure of integrity between the regenerated structure and the remaining tissue were identified. In addition, this treatment affected blastema formation and induced a reduction in the levels of cell proliferation in this structure, as well as a reduction in the number of CD45 and CD11b + immune system cells. On the other hand, blocking ROS production affected the expression of proximo-distal identity genes such as , , , , and other genes such as and in early/mid blastema. Of great interest, the failure in blastema formation, skeletal alterations, as well as the expression of the genes evaluated were rescued by the application of exogenous HO, suggesting that ROS/HO production is necessary from the early stages for proper regeneration and patterning of the limb.
活性氧(ROS)是再生生物学领域备受关注的分子,因为多种动物模型需要产生ROS来促进和支持组织、器官及附属肢体的再生。最近有研究表明,过氧化氢(HO)等ROS的产生是[动物名称]尾部再生所必需的。然而,迄今为止,在该动物模型中,ROS的产生对于肢体再生是否必要尚不清楚。方法:将幼年动物的前肢在近端截断,并在再生过程中使用二氯二氢荧光素二乙酸酯(DCFDA)测定ROS产生的动态变化。使用NADPH氧化酶抑制剂夹竹桃麻素抑制ROS的产生。随后,使用外源性过氧化氢(HO)进行挽救试验。通过阿尔新蓝和茜素红染色评估这些处理对再生肢体大小和骨骼结构的影响,以及对芽基形成、细胞增殖、免疫细胞募集和与近端 - 远端身份相关基因表达的影响。结果:我们的结果表明,在蝾螈模型中抑制截肢后肢体ROS的产生会导致再生出微型肢体,尺骨、桡骨等骨骼元素以及整个 autopod 的大小显著减小。此外,还发现了其他影响,如腕骨数量减少、关节形态缺陷以及再生结构与剩余组织之间的完整性破坏。此外,这种处理影响了芽基形成,并导致该结构中细胞增殖水平降低,以及CD45和CD11b + 免疫系统细胞数量减少。另一方面,阻断ROS的产生影响了早期/中期芽基中近端 - 远端身份基因如[基因名称]、[基因名称]、[基因名称]、[基因名称]、[基因名称]以及其他基因如[基因名称]和[基因名称]的表达。非常有趣的是,通过应用外源性HO挽救了芽基形成失败、骨骼改变以及所评估基因的表达,这表明从早期阶段开始,ROS/HO的产生对于肢体的正常再生和模式形成是必要的。