Deficiency of thyroid hormone receptor protects retinal pigment epithelium and photoreceptors from cell death in a mouse model of age-related macular degeneration.
Deficiency of thyroid hormone receptor protects retinal pigment epithelium and photoreceptors from cell death in a mouse model of age-related macular degeneration.
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DOI：
10.1038/s41419-022-04691-2
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发表时间：
2022-03-21
影响因子：
9
通讯作者：
Ding XQ
中科院分区：
文献类型：
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作者：
Ma H;Yang F;Ding XQ
Age-related macular degeneration (AMD) is the leading cause of vision loss in the elderly. Progressive dystrophy of the retinal pigment epithelium (RPE) and photoreceptors is the characteristic of dry AMD, and oxidative stress/damage plays a central role in the pathogenic lesion of the disease. Thyroid hormone (TH) regulates cell growth, differentiation, and metabolism, and regulates development/function of photoreceptors and RPE in the retina. Population-/patient-based studies suggest an association of high free-serum TH levels with increased risk of AMD. We recently showed that suppressing TH signaling by antithyroid treatment reduces cell damage/death of the RPE and photoreceptors in an oxidative-stress/sodium iodate (NaIO3)-induced mouse model of AMD. This work investigated the effects of TH receptor (THR) deficiency on cell damage/death of the RPE and photoreceptors and the contribution of the receptor subtypes. Treatment with NaIO3 induced RPE and photoreceptor cell death/necroptosis, destruction, and oxidative damage. The phenotypes were significantly diminished in Thrα1−/−, Thrb−/−, and Thrb2−/− mice, compared with that in the wild-type (C57BL/6 J) mice. The involvement of the receptor subtypes varies in the RPE and retina. Deletion of Thrα1 or Thrb protected RPE, rods, and cones, whereas deletion of Thrb2 protected RPE and cones but not rods. Gene-expression analysis showed that deletion of Thrα1 or Thrb abolished/suppressed the NaIO3-induced upregulation of the genes involved in cellular oxidative-stress responses, necroptosis/apoptosis signaling, and inflammatory responses. In addition, THR antagonist effectively protected ARPE-19 cells and hRPE cells from NaIO3-induced cell death. This work demonstrates the involvement of THR signaling in cell damage/death of the RPE and photoreceptors after oxidative-stress challenge and the receptor-subtype contribution. Findings from this work support a role of THR signaling in the pathogenesis of AMD and the strategy of suppressing THR signaling locally in the retina for protection of the RPE/retina in dry AMD.
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影响因子：
6.3
作者：
Ceresini, Graziano;Lauretani, Fulvio;Maggio, Marcello;Ceda, Gian Paolo;Morganti, Simonetta;Usberti, Elisa;Chezzi, Carlo;Valcavi, Rita;Bandinelli, Stefania;Guralnik, Jack M.;Cappola, Anne R.;Valenti, Giorgio;Ferrucci, Luigi
通讯作者：
Ferrucci, Luigi
影响因子：
4.4
作者：
Gopinath, Bamini;Liew, Gerald;Mitchell, Paul
通讯作者：
Mitchell, Paul
影响因子：
16.6
作者：
Handa, James T.;Rickman, Cathy Bowes;Farrer, Lindsay A.
通讯作者：
Farrer, Lindsay A.
DOI：
10.1073/pnas.051454698
发表时间：
2001-03-27
影响因子：
11.1
作者：
Hashimoto, K;Curty, FH;Wondisford, FE
通讯作者：
Wondisford, FE
影响因子：
9
作者：
通讯作者：
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