ArticleNature communications2026
Dynamic cell fate transitions during morphallactic regeneration.
Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Regeneration can proceed through epimorphosis, involving regrowth of lost structures at the amputation site in a proximal-to-distal sequence, or through morphallaxis, which is characterized by extensive tissue remodeling with minimal cell proliferation. While the mechanisms underlying epimorphic regeneration are well studied, the spatiotemporal dynamics of morphallaxis remain less understood. Here we show, using time-course single-cell RNA sequencing (scRNA-seq) of regenerating Hydra tissue, that morphallaxis involves a temporal sequence in the re-emergence of terminal and subterminal cell identities, with transcriptional signatures associated with proximal structures appearing earlier than those of distal structures. We further find that Wnt signaling remains dynamically active at the amputation site throughout regeneration, with its composition changing over time, consistent with a transient regulatory state. Together, these findings provide a high-resolution view of dynamic cell state transitions and signaling activity during morphallactic regeneration and offer a framework for exploring how organizer function and axial patterning are re-established in Hydra.
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