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衰老斑马鱼和翠青鳉鱼的 fins 再生和血管生成受损。

Impaired fin regeneration and angiogenesis in aged zebrafish and turquoise killifish.

机构信息

Turku Bioscience Centre, University of Turku and Åbo Akademi University, FI-25020 Turku, Finland.

Institute of Vertebrate Biology, Czech Academy of Sciences, 60365 Brno, Czech Republic.

出版信息

Biol Open. 2023 Apr 15;12(4). doi: 10.1242/bio.059622. Epub 2023 Apr 7.

Abstract

Impaired wound healing is associated with aging and has significant effects on human health on an individual level, but also on the whole health-care sector. Deficient angiogenesis appears to be involved in the process, but the underlying biology is still poorly understood. This is at least partially being explained by complexity and costs in using mammalian aging models. To understand aging-related vascular biology of impaired wound healing, we used zebrafish and turquoise killifish fin regeneration models. The regeneration of caudal fin after resection was significantly reduced in old individuals in both species. Age-related changes in angiogenesis, vascular density and expression levels of angiogenesis biomarker VEGF-A were observed. Furthermore, the anti-angiogenic drug vascular endothelial growth factor receptor blocking inhibitor SU5416 reduced regeneration, indicating a key role for angiogenesis in the regeneration of aging caudal fin despite aging-related changes in vasculature. Taken together, our data indicate that these fish fin regeneration models are suitable for studying aging-related decline in wound healing and associated alterations in aging vasculature.

摘要

伤口愈合受损与衰老有关,不仅对个体健康,而且对整个医疗保健部门都有重大影响。似乎缺乏血管生成参与了这一过程,但潜在的生物学机制仍知之甚少。这至少部分可以通过使用哺乳动物衰老模型的复杂性和成本来解释。为了了解与衰老相关的伤口愈合受损的血管生物学,我们使用了斑马鱼和翠雀鱼鳍再生模型。在这两个物种中,切除后尾部鳍的再生在老年个体中显著减少。观察到血管生成、血管密度和血管生成生物标志物 VEGF-A 的表达水平的年龄相关变化。此外,抗血管生成药物血管内皮生长因子受体阻断抑制剂 SU5416 减少了再生,表明血管生成在衰老尾部鳍的再生中起着关键作用,尽管血管老化相关变化。综上所述,我们的数据表明,这些鱼类鳍再生模型适合研究与衰老相关的伤口愈合能力下降以及衰老血管的相关改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df11/10120072/ef056ae494bd/biolopen-12-059622-g1.jpg

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