Single-cell analysis uncovers convergence of cell identities during axolotl limb regeneration

Tobias Gerber(Max Planck Institute for Evolutionary Anthropology), Prayag Murawala(Research Institute of Molecular Pathology), Dunja Knapp(Deutsche Forschungsgemeinschaft), Wouter Masselink(Research Institute of Molecular Pathology), Maritta Schuez(Deutsche Forschungsgemeinschaft), Sarah Hermann(Deutsche Forschungsgemeinschaft), Malgorzata Gac-Santel(Max Planck Institute for Evolutionary Anthropology), Sergej Nowoshilow(Research Institute of Molecular Pathology), Jorge Kageyama(Max Planck Institute for Evolutionary Anthropology), Shahryar Khattak(Deutsche Forschungsgemeinschaft), Joshua D. Currie(Deutsche Forschungsgemeinschaft), J. Gray Camp(Max Planck Institute for Evolutionary Anthropology), Elly M. Tanaka(Research Institute of Molecular Pathology), Barbara Treutlein(Max Planck Institute for Evolutionary Anthropology)
Science
September 27, 2018
Cited by 436Open Access
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Abstract

Amputation of the axolotl forelimb results in the formation of a blastema, a transient tissue where progenitor cells accumulate prior to limb regeneration. However, the molecular understanding of blastema formation had previously been hampered by the inability to identify and isolate blastema precursor cells in the adult tissue. We have used a combination of Cre-loxP reporter lineage tracking and single-cell messenger RNA sequencing (scRNA-seq) to molecularly track mature connective tissue (CT) cell heterogeneity and its transition to a limb blastema state. We have uncovered a multiphasic molecular program where CT cell types found in the uninjured adult limb revert to a relatively homogenous progenitor state that recapitulates an embryonic limb bud-like phenotype including multipotency within the CT lineage. Together, our data illuminate molecular and cellular reprogramming during complex organ regeneration in a vertebrate.


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