Max Perutz Labs, Vienna Biocenter Campus (VBC), Vienna, Austria.
University of Vienna, Center for Molecular Biology, Department of Genetics and Microbiology, Vienna, Austria.
Nat Commun. 2024 Nov 18;15(1):9882. doi: 10.1038/s41467-024-54041-3.
Regeneration of missing body parts can be observed in diverse animal phyla, but it remains unclear to which extent these capacities rely on shared or divergent principles. Research into this question requires detailed knowledge about the involved molecular and cellular principles in suitable reference models. By combining single-cell RNA sequencing and mosaic transgenesis in the marine annelid Platynereis dumerilii, we map cellular profiles and lineage restrictions during posterior regeneration. Our data reveal cell-type specific injury responses, re-expression of positional identity factors, and the re-emergence of stem cell signatures in multiple cell populations. Epidermis and mesodermal coelomic tissue produce distinct putative posterior stem cells (PSCs) in the emerging blastema. A novel mosaic transgenesis strategy reveals both developmental compartments and lineage restrictions during regenerative growth. Our work supports the notion that posterior regeneration involves dedifferentiation, and reveals molecular and mechanistic parallels between annelid and vertebrate regeneration.
缺失身体部位的再生可以在不同的动物门中观察到,但这些能力在多大程度上依赖于共同或不同的原则仍不清楚。研究这个问题需要在合适的参考模型中详细了解涉及的分子和细胞原理。通过在海洋环节动物 Platynereis dumerilii 中结合单细胞 RNA 测序和嵌合体转基因,我们描绘了在后再生过程中的细胞特征和谱系限制。我们的数据揭示了特定于细胞类型的损伤反应、位置身份因子的重新表达以及多个细胞群体中干细胞特征的重新出现。表皮和中胚层体腔组织在新形成的芽基中产生不同的潜在后干细胞(PSC)。一种新的嵌合体转基因策略揭示了再生性生长过程中的发育隔室和谱系限制。我们的工作支持后再生涉及去分化的观点,并揭示了环节动物和脊椎动物再生之间的分子和机制相似性。