The Radiobiological Characterization of Human and Porcine Lens Cells Suggests the Importance of the ATM Kinase in Radiation-Induced Cataractogenesis.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
21 08 2023
Historique:
received: 12 07 2023
revised: 14 08 2023
accepted: 17 08 2023
medline: 28 8 2023
pubmed: 26 8 2023
entrez: 26 8 2023
Statut: epublish

Résumé

Studies about radiation-induced human cataractogenesis are generally limited by (1) the poor number of epithelial lens cell lines available (likely because of the difficulties of cell sampling and amplification) and (2) the lack of reliable biomarkers of the radiation-induced aging process. We have developed a mechanistic model of the individual response to radiation based on the nucleoshuttling of the ATM protein (RIANS). Recently, in the frame of the RIANS model, we have shown that, to respond to permanent endo- and exogenous stress, the ATM protein progressively agglutinates around the nucleus attracted by overexpressed perinuclear ATM-substrate protein. As a result, perinuclear ATM crowns appear to be an interesting biomarker of aging. The radiobiological characterization of the two human epithelial lens cell lines available and the four porcine epithelial lens cell lines that we have established showed delayed RIANS. The BFSP2 protein, found specifically overexpressed around the lens cell nucleus and interacting with ATM, may be a specific ATM-substrate protein facilitating the formation of perinuclear ATM crowns in lens cells. The perinuclear ATM crowns were observed inasmuch as the number of culture passages is high. Interestingly, 2 Gy X-rays lead to the transient disappearance of the perinuclear ATM crowns. Altogether, our findings suggest a strong influence of the ATM protein in radiation-induced cataractogenesis.

Identifiants

pubmed: 37626928
pii: cells12162118
doi: 10.3390/cells12162118
pmc: PMC10453874
pii:
doi:

Substances chimiques

Ataxia Telangiectasia Mutated Proteins EC 2.7.11.1
ATM protein, human EC 2.7.11.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Joëlle Al-Choboq (J)

INSERM U1296 Unit "Radiation: Defense, Health, Environment", 28 Rue Laennec, 69008 Lyon, France.

Thibaud Mathis (T)

Ophtalmology Department, Hospices Civils de Lyon, General University Hospital of Croix-Rousse, 103 Grande Rue Croix Rousse, 69004 Lyon, France.
MATEIS Laboratory, CNRS UMR5510, INSA, Université Claude-Bernard Lyon 1, Campus de la Doua, 69100 Villeurbanne, France.

Juliette Restier-Verlet (J)

INSERM U1296 Unit "Radiation: Defense, Health, Environment", 28 Rue Laennec, 69008 Lyon, France.

Laurène Sonzogni (L)

INSERM U1296 Unit "Radiation: Defense, Health, Environment", 28 Rue Laennec, 69008 Lyon, France.

Laura El Nachef (L)

INSERM U1296 Unit "Radiation: Defense, Health, Environment", 28 Rue Laennec, 69008 Lyon, France.

Adeline Granzotto (A)

INSERM U1296 Unit "Radiation: Defense, Health, Environment", 28 Rue Laennec, 69008 Lyon, France.

Michel Bourguignon (M)

INSERM U1296 Unit "Radiation: Defense, Health, Environment", 28 Rue Laennec, 69008 Lyon, France.
Department of Biophysics and Nuclear Medicine, Université Paris Saclay Versailles St Quentin-en-Yvelines, 78035 Versailles, France.

Nicolas Foray (N)

INSERM U1296 Unit "Radiation: Defense, Health, Environment", 28 Rue Laennec, 69008 Lyon, France.

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Classifications MeSH