Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10495/40525
Título : Rapamycin Eyedrops Increased CD4+Foxp3+ Cells and Prevented Goblet Cell Loss in the Aged Ocular Surface
Autor : Trujillo Vargas, Claudia Milena
Kutlehria, Shallu
Hernández, Humberto
de Souza, Rodrigo G
Lee, Andrea
Yu, Zhiyuan
Pflugfelder, Stephen C
Singh, Mandip
de Paiva, Cintia S
metadata.dc.subject.*: Aging
Envejecimiento
Autophagy-Related Protein-1 Homolog
Homólogo de la Proteína 1 Relacionada con la Autofagia
CD4 Antigens
Antígenos CD4
Cell Lineage
Linaje de la Célula
Conjunctiva
Conjuntiva
Cornea
Córnea
Disease Models, Animal
Modelos Animales de Enfermedad
Dry Eye Syndromes
Síndromes de Ojo Seco
Forkhead Transcription Factors
Factores de Transcripción Forkhead
Goblet Cells
Células Caliciformes
Inflammation
Inflamación
Interferon-gamma
Interferón gamma
Leukocyte Common Antigens
Antígenos Comunes de Leucocito
Ophthalmic Solutions
Soluciones Oftálmicas
Sirolimus
Sirolimus
Vascular Endothelial Growth Factor A
Factor A de Crecimiento Endotelial Vascular
https://id.nlm.nih.gov/mesh/D000375
https://id.nlm.nih.gov/mesh/D000071189
https://id.nlm.nih.gov/mesh/D015704
https://id.nlm.nih.gov/mesh/D019070
https://id.nlm.nih.gov/mesh/D003228
https://id.nlm.nih.gov/mesh/D003315
https://id.nlm.nih.gov/mesh/D004195
https://id.nlm.nih.gov/mesh/D015352
https://id.nlm.nih.gov/mesh/D051858
https://id.nlm.nih.gov/mesh/D020397
https://id.nlm.nih.gov/mesh/D007249
https://id.nlm.nih.gov/mesh/D007371
https://id.nlm.nih.gov/mesh/D017493
https://id.nlm.nih.gov/mesh/D009883
https://id.nlm.nih.gov/mesh/D020123
https://id.nlm.nih.gov/mesh/D042461
Fecha de publicación : 2020
Editorial : MDPI
Citación : Trujillo-Vargas CM, Kutlehria S, Hernandez H, de Souza RG, Lee A, Yu Z, Pflugfelder SC, Singh M, de Paiva CS. Rapamycin Eyedrops Increased CD4+Foxp3+ Cells and Prevented Goblet Cell Loss in the Aged Ocular Surface. Int J Mol Sci. 2020 Nov 24;21(23):8890. doi: 10.3390/ijms21238890.
Resumen : ABSTRACT: Inflammation and oxidative stress accompany aging. This study investigated the interplay between oxidative stress and inflammation in the lacrimal gland. C57BL/6 mice were used at 2 to 3, 12, and 24 months of age. Nuclear factor erythroid derived-2-related factor 2 (Nrf2)-/- and corresponding wild-type mice were used at 2 to 3 and 12 to 13 months of age. A separate group of 15.5 to 17 months of age C57BL/6 mice received a diet containing an Nrf2 inducer (Oltipraz) for 8 weeks. Aged C57BL/6 lacrimal glands showed significantly greater lymphocytic infiltration, higher levels of MHC II, IFN-γ, IL-1β, TNF-α, and cathepsin S (Ctss) mRNA transcripts, and greater nitrotyrosine and 4-hydroxynonenal protein. Young Nrf2-/- mice showed an increase in IL-1β, IFN-γ, MHC II, and Ctss mRNA transcripts compared with young wild-type mice and greater age-related changes at 12 to 13 months of age. Oltipraz diet significantly decreased nitrotyrosine and 4-hydroxynonenal and decreased the expression of IL-1β and TNF-α mRNA transcripts, while decreasing the frequency of CD45+CD4+ cells in lacrimal glands and significantly increasing conjunctival goblet cell density compared with a standard diet. The findings provide novel insight into the development of chronic, low-grade inflammation and oxidative stress in age-related dry eye. New therapies targeting oxidative stress pathways will be valuable in treating age-related dry eye.
metadata.dc.identifier.eissn: 1422-0067
ISSN : 1661-6596
metadata.dc.identifier.doi: 10.3390/ijms21238890
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