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• W3209865857 endingPage "103269" @default.
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• W3209865857 abstract "Fibrosis-driven solid organ failure is an enormous burden on global health. Spiny mice (Acomys) are terrestrial mammals that can regenerate severe skin wounds without scars to avoid predation. Whether spiny mice also regenerate internal organ injuries is unknown. Here, we show that despite equivalent acute obstructive or ischemic kidney injury, spiny mice fully regenerate nephron structure and organ function without fibrosis, whereas C57Bl/6 or CD1 mice progress to complete organ failure with extensive renal fibrosis. Two mechanisms for vertebrate regeneration have been proposed that emphasize either extrinsic (pro-regenerative macrophages) or intrinsic (surviving cells of the organ itself) controls. Comparative transcriptome analysis revealed that the Acomys genome appears poised at the time of injury to initiate regeneration by surviving kidney cells, whereas macrophage accumulation was not detected until about day 7. Thus, we provide evidence for rapid activation of a gene expression signature for regenerative wound healing in the spiny mouse kidney." @default.
• W3209865857 created "2021-11-08" @default.
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• W3209865857 date "2021-11-01" @default.
• W3209865857 modified "2023-10-18" @default.
• W3209865857 title "Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis" @default.
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• W3209865857 doi "https://doi.org/10.1016/j.isci.2021.103269" @default.
• W3209865857 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8609232" @default.
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