tBid-Mediated Genetic Ablation of Connective Tissue Cells Reveals Their Key Regulatory Function During Limb Regeneration in Axolotls

AI Summary

Established an inducible Cre-LoxP tBid ablation system enabling efficient, targeted elimination of muscle and muscle stem cells via transient electroporation or genetic methods.
Ablating connective tissue early in regeneration delays regrowth and causes proximal limb segment loss while sparing distal hand differentiation, mirroring developmental defects.
scRNA-seq reveals proximal to distal CT transitions and distinct CT1 subtypes; loss of CT1-a and delayed CT1 progenitor conversion drive morphological defects and altered proliferation.

Adv Sci (Weinh). 2026 May 27:e24339. doi: 10.1002/advs.202524339. Online ahead of print.

ABSTRACT

Vertebrate limb regeneration in adulthood is a fascinating phenomenon unique to salamanders, requiring precise coordination and interaction of various cell types. Connective tissue (CT) constitutes a major component of the limb and serves as the primary reservoir of positional information during regeneration. However, the role and extent of CT cell contribution remain largely undefined. Here we develop an inducible Cre-LoxP-mediated tBid cell ablation system in axolotls and demonstrate efficient elimination of targeted muscle tissue and muscle stem cells through transient electroporation or genetic approach. Ablation of CT cells at early regeneration stages results in delayed regeneration and loss of proximal limb segments (e.g., upper and lower limb), with minimal impact on hand differentiation. CT ablation during development yields similar defects, supporting an essential role for CT cells in determining the positional identity of developing and regenerating limb structures. Further single-cell RNA-sequencing (scRNA-seq) reveals a progressive proximal-to-distal transition among CT cells and identifies distinct CT subtypes contributing to proximal and distal segments. CT ablation reduces differentiated CT1-a subpopulation maintaining proximal identity throughout regeneration, and delays distal transformation in proliferative CT1 progenitors. These cellular shifts likely explain the observed morphological deficits. Moreover, differentiated CT1 cells enhance interactions with surrounding cells after CT ablation to modulate adaptive proliferation in other populations (e.g., muscle stem cells). Our work establishes a tBid-based ablation strategy for functional studies of CT and other cell types in axolotls and demonstrates pivotal roles of CT cells in limb regeneration.

PMID:42201602 | DOI:10.1002/advs.202524339

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