isl1a coordinates onset and termination of regeneration of the zebrafish lateral line

Regenerative capacity varies widely across tissues and species. Most regeneration studies have focused on identifying genes and pathways that promote regeneration, whereas mechanisms that inhibit regeneration to enforce organ size control and prevent excessive proliferation remain less well defined. Here, we identify isl1a as a dynamically expressed negative regulator of lateral line hair cell regeneration. isl1a is highly expressed during homeostasis but becomes transiently downregulated following hair cell loss. Loss of isl1a leads to proliferative expansion of support cells, producing enlarged sensory organs with increased hair cell numbers after injury. Mechanistically, isl1a downregulation increases chromatin accessibility at pro-proliferative loci, including AP-1 transcription factors, accompanied by sustained expression of injury- and regeneration-responsive genes. Together, these findings demonstrate that injury-induced downregulation of isl1a promotes the initiation of regeneration, while its subsequent re-expression restricts the duration of the response, thereby fine-tuning hair cell regeneration and maintaining appropriate support cell numbers.

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Publication Details

Journal
npj Regenerative Medicine
Published
2026-07-01
DOI
https://doi.org/10.1038/s41536-026-00489-4
Primary Topic
Developmental Biology and Gene Regulation
Type
article
Field-Weighted Citation Impact
0.00

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article

isl1a coordinates onset and termination of regeneration of the zebrafish lateral line

Aurélie Hintermann, Nhung T. T. Tran, Tatjana Piotrowski, Mark E. Lush et al.
npj Regenerative Medicine
Developmental Biology and Gene Regulation
article

isl1a coordinates onset and termination of regeneration of the zebrafish lateral line

Aurélie Hintermann, Nhung T. T. Tran, Tatjana Piotrowski, Mark E. Lush, Paloma Meneses-Giles, Kaelan J. Brennan
article en

Abstract

Regenerative capacity varies widely across tissues and species. Most regeneration studies have focused on identifying genes and pathways that promote regeneration, whereas mechanisms that inhibit regeneration to enforce organ size control and prevent excessive proliferation remain less well defined. Here, we identify isl1a as a dynamically expressed negative regulator of lateral line hair cell regeneration. isl1a is highly expressed during homeostasis but becomes transiently downregulated following hair cell loss. Loss of isl1a leads to proliferative expansion of support cells, producing enlarged sensory organs with increased hair cell numbers after injury. Mechanistically, isl1a downregulation increases chromatin accessibility at pro-proliferative loci, including AP-1 transcription factors, accompanied by sustained expression of injury- and regeneration-responsive genes. Together, these findings demonstrate that injury-induced downregulation of isl1a promotes the initiation of regeneration, while its subsequent re-expression restricts the duration of the response, thereby fine-tuning hair cell regeneration and maintaining appropriate support cell numbers.

npj Regenerative Medicine
Stowers Institute for Medical Research (US)
Stowers Institute for Medical Research, National Institutes of Health, National Institute on Deafness and Other Communication Disorders
Openalex Percentile: Top 12%
Developmental Biology and Gene Regulation
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