A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stress.

Details

Serval ID
serval:BIB_AE7ADE4503CB
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stress.
Journal
Disease models & mechanisms
Author(s)
Rissone A., Jimenez E., Bishop K., Carrington B., Slevin C., Wincovitch S.M., Sood R., Candotti F., Burgess S.M.
ISSN
1754-8411 (Electronic)
ISSN-L
1754-8403
Publication state
Published
Issued date
20/12/2019
Peer-reviewed
Oui
Volume
12
Number
12
Language
english
Notes
Publication types: Journal Article ; Research Support, N.I.H., Intramural
Publication Status: epublish
Abstract
Mutations in the gene AK2 are responsible for reticular dysgenesis (RD), a rare and severe form of primary immunodeficiency in children. RD patients have a severely shortened life expectancy and without treatment die, generally from sepsis soon after birth. The only available therapeutic option for RD is hematopoietic stem cell transplantation (HSCT). To gain insight into the pathophysiology of RD, we previously created zebrafish models for Ak2 deficiencies. One of the clinical features of RD is hearing loss, but its pathophysiology and causes have not been determined. In adult mammals, sensory hair cells of the inner ear do not regenerate; however, their regeneration has been observed in several non-mammalian vertebrates, including zebrafish. Therefore, we used our RD zebrafish models to determine whether Ak2 deficiency affects sensory organ development and/or hair cell regeneration. Our studies indicated that Ak2 is required for the correct development, survival and regeneration of sensory hair cells. Interestingly, Ak2 deficiency induces the expression of several oxidative stress markers and it triggers an increased level of cell death in the hair cells. Finally, we show that glutathione treatment can partially rescue hair cell development in the sensory organs in our RD models, pointing to the potential use of antioxidants as a therapeutic treatment supplementing HSCT to prevent or ameliorate sensorineural hearing deficits in RD patients.
Keywords
Adenylate Kinase/metabolism, Alleles, Animals, Animals, Genetically Modified, Cell Death, Cell Line, Crosses, Genetic, Disease Models, Animal, Gene Expression Regulation, Developmental, Glutathione/metabolism, Green Fluorescent Proteins/metabolism, Hair Cells, Auditory/physiology, Hearing Loss, Sensorineural/metabolism, Hematopoietic Stem Cell Transplantation, Leukopenia/genetics, Leukopenia/metabolism, Microscopy, Confocal, Oxidative Stress, Phenotype, Regeneration, Severe Combined Immunodeficiency/genetics, Severe Combined Immunodeficiency/metabolism, Stress, Physiological, Zebrafish, Ak2, Antioxidants, Hair cells, Hearing loss, Lateral line, Reticular dysgenesis, SCID
Pubmed
Web of science
Open Access
Yes
Create date
29/11/2019 21:46
Last modification date
18/09/2020 6:26
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