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Differences in Unfolded Protein Response Pathway Activation in the Lenses of Three Types of Cataracts

PURPOSE: To investigate the activation of three unfolded protein response (UPR) pathways in the lenses of age-related, high myopia-related and congenital cataracts. METHODS AND MATERIALS: Lens specimens were collected from patients during small incision cataract surgery. Lenses from young cadaver ey...

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Detalles Bibliográficos
Autores principales: Yang, Jing, Zhou, Sheng, Gu, Jianjun, Wang, Yujuan, Guo, Minfei, Liu, Yizhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475046/
https://www.ncbi.nlm.nih.gov/pubmed/26091066
http://dx.doi.org/10.1371/journal.pone.0130705
Descripción
Sumario:PURPOSE: To investigate the activation of three unfolded protein response (UPR) pathways in the lenses of age-related, high myopia-related and congenital cataracts. METHODS AND MATERIALS: Lens specimens were collected from patients during small incision cataract surgery. Lenses from young cadaver eyes were collected as normal controls. Real-time PCR and Western blotting were performed to detect the expression of GRP78, p-eIF2α, spliced XBP1, ATF6, ATF4 and p-IRE1α in the lenses of normal human subjects and patients with age-related, myopia-related or congenital cataracts. RESULTS: In the lenses of the age-related and high myopia-related cataract groups, the protein levels of ATF6, p-eIF2α and p-IRE1α and the gene expression levels of spliced XBP1, GRP78, ATF6 and ATF4 were greatly increased. Additionally, in the congenital cataract group, the protein levels of p-eIF2α and p-IRE1α and the gene expression levels of spliced XBP1, GRP78 and ATF4 were greatly increased. However, the protein and gene expression levels of ATF6 were not up-regulated in the congenital cataract group compared with the normal control group. CONCLUSIONS: The UPR is activated via different pathways in the lenses of age-related, high myopia-related and congenital cataracts. UPR activation via distinct pathways might play important roles in cataractogenesis mechanisms in different types of cataracts.