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分泌抑制剂驱动非洲爪蟾肢体再生能力的丧失。

Secreted inhibitors drive the loss of regeneration competence in Xenopus limbs.

机构信息

Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.

Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK.

出版信息

Development. 2021 Jun 1;148(11). doi: 10.1242/dev.199158. Epub 2021 Jun 9.

Abstract

Absence of a specialized wound epidermis is hypothesized to block limb regeneration in higher vertebrates. However, the factors preventing its formation in regeneration-incompetent animals are poorly understood. To characterize the endogenous molecular and cellular regulators of specialized wound epidermis formation in Xenopus laevis tadpoles, and the loss of their regeneration competency during development, we used single-cell transcriptomics and ex vivo regenerating limb cultures. Transcriptomic analysis revealed that the specialized wound epidermis is not a novel cell state, but a re-deployment of the apical-ectodermal-ridge (AER) programme underlying limb development. Enrichment of secreted inhibitory factors, including Noggin, a morphogen expressed in developing cartilage/bone progenitor cells, are identified as key inhibitors of AER cell formation in regeneration-incompetent tadpoles. These factors can be overridden by Fgf10, which operates upstream of Noggin and blocks chondrogenesis. These results indicate that manipulation of the extracellular environment and/or chondrogenesis may provide a strategy to restore regeneration potential in higher vertebrates.

摘要

人们假设缺乏专门的伤口表皮会阻止高等脊椎动物的肢体再生。然而,对于阻止其在再生能力不足的动物中形成的因素知之甚少。为了研究非洲爪蟾蝌蚪中专门的伤口表皮形成的内源性分子和细胞调节剂,以及它们在发育过程中丧失再生能力的原因,我们使用了单细胞转录组学和体外再生肢体培养技术。转录组分析表明,专门的伤口表皮不是一种新的细胞状态,而是肢发育中顶外胚层嵴(AER)程序的重新部署。包括 Noggin 在内的分泌抑制因子的富集,Noggin 是一种在发育中的软骨/骨祖细胞中表达的形态发生素,被鉴定为再生能力不足的蝌蚪中 AER 细胞形成的关键抑制剂。这些因子可以被 Fgf10 逆转,Fgf10 在上游起作用并阻止软骨生成。这些结果表明,对细胞外环境和/或软骨生成的操作可能为恢复高等脊椎动物的再生潜力提供一种策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e359/8217717/0744711964a2/develop-148-199158-g1.jpg

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