Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, 04103 Leipzig, Germany.
Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Campus-Vienna-Biocenter 1, 1030 Vienna, Austria.
Science. 2018 Oct 26;362(6413). doi: 10.1126/science.aaq0681. Epub 2018 Sep 27.
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.
蝾螈前肢截肢会导致芽基的形成,芽基是一种短暂的组织,祖细胞在肢体再生前在此聚集。然而,由于无法在成年组织中识别和分离芽基前体细胞,因此之前对芽基形成的分子理解一直受到阻碍。我们结合了 Cre-loxP 报告基因谱系追踪和单细胞信使 RNA 测序 (scRNA-seq),对成熟结缔组织 (CT) 细胞异质性及其向肢体芽基状态的转变进行了分子追踪。我们发现了一个多相的分子程序,即在未受伤的成年肢体中发现的 CT 细胞类型恢复到相对同质的祖细胞状态,该状态再现了胚胎肢芽样表型,包括 CT 谱系内的多能性。总之,我们的数据阐明了脊椎动物复杂器官再生过程中的分子和细胞重编程。