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感光细胞持续表达 IL-35,并促进眼部免疫特惠。

Photoreceptor Cells Constitutively Express IL-35 and Promote Ocular Immune Privilege.

机构信息

Molecular Immunology Section, Laboratory of Immunology, National Eye Institute (NEI), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

Immunoregulation Section, Laboratory of Immunology, National Eye Institute (NEI), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

出版信息

Int J Mol Sci. 2022 Jul 24;23(15):8156. doi: 10.3390/ijms23158156.

DOI:10.3390/ijms23158156
PMID:35897732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9351654/
Abstract

Interleukin-27 is constitutively secreted by microglia in the retina or brain, and upregulation of IL-27 during neuroinflammation suppresses encephalomyelitis and autoimmune uveitis. However, while IL-35 is structurally and functionally similar to IL-27, the intrinsic roles of IL-35 in CNS tissues are unknown. Thus, we generated IL-35/YFP-knock-in reporter mice (p35-KI) and demonstrated that photoreceptor neurons constitutively secrete IL-35, which might protect the retina from persistent low-grade inflammation that can impair photoreceptor functions. Furthermore, the p35-KI mouse, which is hemizygous at the locus, develops more severe uveitis because of reduced IL-35 expression. Interestingly, onset and exacerbation of uveitis in p35-KI mice caused by extravasation of proinflammatory Th1/Th17 lymphocytes into the retina were preceded by a dramatic decrease of IL-35, attributable to massive death of photoreceptor cells. Thus, while inflammation-induced death of photoreceptors and loss of protective effects of IL-35 exacerbated uveitis, our data also suggest that constitutive production of IL-35 in the retina might have housekeeping functions that promote sterilization immunity in the neuroretina and maintain ocular immune privilege.

摘要

白细胞介素-27 由视网膜或大脑中的小胶质细胞持续分泌,神经炎症期间白细胞介素-27 的上调抑制了脑脊髓炎和自身免疫性葡萄膜炎。然而,虽然白细胞介素-35 在结构和功能上与白细胞介素-27 相似,但白细胞介素-35 在中枢神经系统组织中的内在作用尚不清楚。因此,我们生成了白细胞介素-35/YFP 敲入报告小鼠(p35-KI),并证实光感受器神经元持续分泌白细胞介素-35,这可能保护视网膜免受持续低度炎症的损害,因为持续低度炎症会损害光感受器功能。此外,由于白细胞介素-35 表达减少,p35-KI 小鼠(在 基因座上为半合子)发生更严重的葡萄膜炎。有趣的是,p35-KI 小鼠葡萄膜炎的发病和恶化是由于促炎 Th1/Th17 淋巴细胞渗出到视网膜引起的,这与光感受器细胞的大量死亡有关。因此,虽然炎症诱导的光感受器细胞死亡和白细胞介素-35 保护作用的丧失加剧了葡萄膜炎,但我们的数据还表明,视网膜中白细胞介素-35 的持续产生可能具有管家功能,促进神经视网膜的无菌免疫并维持眼部免疫特权。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/07488e80538d/ijms-23-08156-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/870ed809f807/ijms-23-08156-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/14e8c87f44a5/ijms-23-08156-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/7877230541d8/ijms-23-08156-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/a63f5df7d875/ijms-23-08156-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/07488e80538d/ijms-23-08156-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/870ed809f807/ijms-23-08156-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/14e8c87f44a5/ijms-23-08156-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d0/9351654/7877230541d8/ijms-23-08156-g003.jpg
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本文引用的文献

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