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.
Authors
- Aurélie Hintermann (ORCID: https://orcid.org/0000-0002-4015-4165)
- Nhung T. T. Tran (ORCID: https://orcid.org/0000-0002-9660-8904)
- Tatjana Piotrowski (ORCID: https://orcid.org/0000-0001-8098-2574)
- Mark E. Lush (ORCID: https://orcid.org/0000-0002-2128-524X)
- Paloma Meneses-Giles
- Kaelan J. Brennan
Institutions
- Stowers Institute for Medical Research (US)
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
Funders
- Stowers Institute for Medical Research
- National Institutes of Health
- National Institute on Deafness and Other Communication Disorders