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Systemic and local lipid adaptations underlie regeneration in Drosophila melanogaster and Ambystoma mexicanum.


ABSTRACT: In regenerating tissues, synthesis and remodeling of membranes rely on lipid turnover and transport. Our study addresses lipid adaptations in intestinal regeneration of Drosophila melanogaster and limb regeneration of Ambystoma mexicanum. We found changes in lipid profiles at different locations: transport, storage organs and regenerating tissues. We demonstrate that attenuating insulin signaling, exclusively in fat storage, inhibits the regeneration-specific response in both the fat storage and the regenerating tissue in Drosophila. Furthermore, in uninjured axolotls we found sex-specific lipid profiles in both storage and circulation, while in regenerating animals these differences subside. The regenerating limb presents a unique sterol profile, albeit with no sex differences. We postulate that regeneration triggers a systemic response, where organs storing lipids play a significant role in the regulation of systemic lipid traffic. Second, that this response may be an active and well-regulated mechanism, as observed when homeostatic sex-differences disappear in regenerating salamanders.

SUBMITTER: Kubler IC 

PROVIDER: S-EPMC11522293 | biostudies-literature | 2024 Oct

REPOSITORIES: biostudies-literature

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Systemic and local lipid adaptations underlie regeneration in Drosophila melanogaster and Ambystoma mexicanum.

Kübler Ines C IC   Kretzschmar Jenny J   Arredondo-Lasso Maria Nieves MN   Keeley Sean D SD   Rößler Luca Claudia LC   Ganss Katharina K   Sandoval-Guzmán Tatiana T   Brankatschk Marko M  

NPJ Regenerative medicine 20241029 1


In regenerating tissues, synthesis and remodeling of membranes rely on lipid turnover and transport. Our study addresses lipid adaptations in intestinal regeneration of Drosophila melanogaster and limb regeneration of Ambystoma mexicanum. We found changes in lipid profiles at different locations: transport, storage organs and regenerating tissues. We demonstrate that attenuating insulin signaling, exclusively in fat storage, inhibits the regeneration-specific response in both the fat storage and  ...[more]

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