Female mice reaching exceptionally high old age have preserved 20S proteasome activities

Oxidized, damaged and misfolded proteins accumulate during aging and contribute to impaired cell function and tissue homeodynamics. Damaged proteins are degraded by cellular clearance mechanisms like the 20S proteasome. Aging relates to low 20S proteasome function, whereas long-lived species show hi...

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Detalles Bibliográficos
Autores: Martínez de Toda Cabeza, Irene, Rattan, Suresh I. S., Fuente del Rey, Mónica de la, Arranz Salas, Lorena
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/4771
Acceso en línea:https://hdl.handle.net/20.500.14352/4771
Access Level:acceso abierto
Palabra clave:577.112
612.67
591.1
577.27
Aging
Healthy aging
Exceptionally old
20S proteasome
Caspase-like activity
Chymotrypsinlike activity
Inmunología
Bioquímica (Biología)
Fisiología animal (Biología)
2412 Inmunología
2302 Bioquímica
2401.13 Fisiología Animal
Descripción
Sumario:Oxidized, damaged and misfolded proteins accumulate during aging and contribute to impaired cell function and tissue homeodynamics. Damaged proteins are degraded by cellular clearance mechanisms like the 20S proteasome. Aging relates to low 20S proteasome function, whereas long-lived species show high levels. However, contradictory results exist depending on the tissue or cell type and it is unknown how the 20S proteasome functions in exceptionally old mice. The aim of this study was to investigate two proteasome activities (caspase-like and chymotrypsin-like) in several tissues (lung, heart, axillary lymph nodes, liver, kidney) and cells (peritoneal leukocytes) from adult (28 ± 4 weeks, n = 12), old (76 ± 4 weeks, n = 9) and exceptionally old (128 ± 4 weeks, n = 9) BALB/c female mice. The results show different age-related changes depending on the tissue and the activity considered, so there is no universal decline in proteasome function with age in female mice. Interestingly, exceptionally old mice displayed better maintained proteasome activities, suggesting that preserved 20S proteasome is associated with successful aging.