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Microglia modulation by TGF-β1 protects cones in mouse models of retinal degeneration
Sean K. Wang, … , Yunlu Xue, Constance L. Cepko
Sean K. Wang, … , Yunlu Xue, Constance L. Cepko
Published April 30, 2020
Citation Information: J Clin Invest. 2020;130(8):4360-4369. https://doi.org/10.1172/JCI136160.
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Research Article Inflammation Ophthalmology

Microglia modulation by TGF-β1 protects cones in mouse models of retinal degeneration

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Abstract

Retinitis pigmentosa (RP) is a genetically heterogenous group of eye diseases in which initial degeneration of rods triggers secondary degeneration of cones, leading to significant loss of daylight, color, and high-acuity vision. Gene complementation with adeno-associated viral (AAV) vectors is one strategy to treat RP. Its implementation faces substantial challenges, however; for example, the tremendous number of loci with causal mutations. Gene therapy targeting secondary cone degeneration is an alternative approach that could provide a much-needed generic treatment for many patients with RP. Here, we show that microglia are required for the upregulation of potentially neurotoxic inflammatory factors during cone degeneration in RP, creating conditions that might contribute to cone dysfunction and death. To ameliorate the effects of such factors, we used AAV vectors to express isoforms of the antiinflammatory cytokine transforming growth factor beta (TGF-β). AAV-mediated delivery of TGF-β1 rescued degenerating cones in 3 mouse models of RP carrying different pathogenic mutations. Treatment with TGF-β1 protected vision, as measured by 2 behavioral assays, and could be pharmacologically disrupted by either depleting microglia or blocking the TGF-β receptors. Our results suggest that TGF-β1 may be broadly beneficial for patients with cone degeneration, and potentially other forms of neurodegeneration, through a pathway dependent upon microglia.

Authors

Sean K. Wang, Yunlu Xue, Constance L. Cepko

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Figure 4

Role of retinal microglia in AAV8-TGFB1-mediated cone survival.

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Role of retinal microglia in AAV8-TGFB1-mediated cone survival.
(A) mRNA...
(A) mRNA expression of indicated genes in FVB (rd1) retinas (n = 4–5) treated with AAV8-GFP or AAV8-GFP plus AAV8-TGFB1. Fold changes are relative to untreated WT (sighted FVB) retinas. Representative images (B) and quantification (C) of IBA1-positive microglia in the ONL of P40 rd1 retinas (n = 6–7) treated with AAV8-GFP or AAV8-GFP plus AAV8-TGFB1. Scale bar: 50 μm. (D) Volcano plot of up- and downregulated genes in microglia sorted from P30 rd1 retinas (n = 7) after treatment with AAV8-GFP plus AAV8-TGFB1 relative to AAV8-GFP only. Dotted lines indicate adjusted P < 0.05 and log2 fold change >0.4. (E) Normalized RNA-seq counts for expression of Tgfbr1 and Tgfbr2 in microglia versus nonmicroglia cells from P30 rd1 retinas (n = 4–14). (F) Immunostaining for TGFBR2 in rd1 CX3CR1GFP/+ retinas (n = 2). Arrowheads indicate colocalization of TGFBR2 with a CX3CR1-positive microglia in the ONL. Scale bar: 10 μm. (G) Quantification of GFP-positive cones in central retinas of rd1 mice after 30 days of microglia depletion with PLX5622 (n = 16) or inhibition of TGFBR1/2 with LY364947 and SB431542 (n = 16). Data for untreated groups are taken from Figure 2E. Data shown are mean ± SEM. ***P < 0.001, ****P < 0.0001 by 2-tailed Student’s t test with Bonferroni’s correction for A and G, 2-tailed Student’s t test for C and E. INL, inner nuclear layer.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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