Secreted inhibitors drive the loss of regeneration competence in Xenopus limbs

Author:

Aztekin Can12ORCID,Hiscock Tom W.134ORCID,Gurdon John12ORCID,Jullien Jerome125ORCID,Marioni John367ORCID,Simons Benjamin David189ORCID

Affiliation:

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

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

3. Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge CB2 0RE, UK

4. Institute of Medical Sciences, Foresterhill Health Campus, University of Aberdeen, Aberdeen AB25 2ZD, UK

5. Nantes Université, Inserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, F-44000 Nantes, France

6. EMBL–European Bioinformatics Institute, Wellcome Genome Campus, Cambridge CB10 1SA, UK

7. Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge CB10 1SA, UK

8. Department of Applied Mathematics and Theoretical Physics, Centre for Mathematical Sciences, University of Cambridge, Cambridge CB3 0WA, UK

9. Wellcome Trust Centre for Stem Cell Research, University of Cambridge, Cambridge CB2 0AW, UK

Abstract

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.

Funder

University of Cambridge

Cambridge Trust

Wellcome Trust

European Molecular Biology Organization

Royal Society

European Molecular Biology Laboratory

Cancer Research UK

Medical Research Council

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3