SAR131675抑制VEGFR-3可减少小鼠狼疮肾炎模型的肾脏炎症和淋巴管生成。

IF 6.1 2区 生物学 Q1 CELL BIOLOGY
Tian Wang, Wenjia Li, Ji-Hyun Yeom, Zhiheng Liu, Kyoung Min Kim, Kyung Pyo Kang
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,以免疫复合物沉积和多器官炎症细胞浸润为特征。大约一半的狼疮患者有肾炎。淋巴管生成是淋巴管(lv)的增殖,它调节组织液稳态和免疫细胞运输,响应组织环境。在本研究中,我们评估了选择性VEGFR-3抑制剂SAR131675通过调节炎症和淋巴管生成对小鼠狼疮性肾炎模型的治疗作用。我们对活检证实的狼疮性肾炎进行了D2-40免疫组织化学染色,D2-40是人淋巴内皮细胞的标记物。动物实验选用7 ~ 8周龄雄性BALB/c小鼠。为了诱导狼疮样模型,在8周的治疗过程中,每隔一天刮除小鼠背部皮肤,用100 μL丙酮溶雷西喹莫特100 μg局部治疗。我们进行了肾脏组织学和免疫荧光检查,检查炎症细胞和淋巴管。我们还进行了qRT-PCR和Western blot分析,以评估炎症细胞因子和趋化因子,淋巴管生成因子和TLR7/ I型IFN反应。一项人体研究发现,修订后的ISN/RPS LN组织病理学分类和修订后的NIH活性指数越高,在小管间质区表达的D2-40(+)淋巴管越多。口服SAR131675治疗抑制VEGFR-3可降低雷西喹莫引起的狼疮模型小鼠肾小球和小管间质炎症,并减弱LYVE-1(+)淋巴管表达。SAR131675通过调节TLR7/MyD88/IFN-α的表达,降低瑞奇莫德诱导的促炎细胞因子和趋化因子的升高。本研究提示通过抑制VEGFR-3靶向淋巴增生治疗狼疮性肾炎的潜力。淋巴网络的调节可能为治疗慢性炎症和减轻肾脏自身免疫反应提供一种新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of VEGFR-3 by SAR131675 decreases renal inflammation and lymphangiogenesis in the murine lupus nephritis model.

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by immune-complex deposits and inflammatory cell infiltrations in multiple organs. Approximately half of lupus patients have nephritis. Lymphangiogenesis is the proliferation of lymphatic vessels (LVs), which regulate tissue fluid homeostasis and immune cell trafficking, responding to the tissue environment. In this study, we evaluated the therapeutic effect of SAR131675, a selective VEGFR-3 inhibitor, on the murine lupus nephritis model by regulating inflammation and lymphangiogenesis. We evaluated biopsy-proven lupus nephritis with immunohistochemical staining for D2-40, a marker for human lymphatic endothelial cells. For animal experiments, 7- to 8-week-old male BALB/c mice were used. For the induction of a lupus-like model, the dorsal skin of mice was shaved and given topical treatment every other day with 100 μg resiquimod dissolved in 100 μL acetone during the 8-week treatment. We had renal histology and immunofluorescent study for inflammatory cells and lymphatic vessels. We also had a qRT-PCR and Western blot analysis to evaluate inflammatory cytokines and chemokines, lymphangiogenic factors, and TLR7/type I IFN response. A human study found that the higher the revised ISN/RPS LN histopathological classification and modified NIH activity indexes, the more D2-40 (+) lymphatic vessels were expressed in the tubulointerstitial areas. Inhibition of VEGFR-3 by oral SAR131675 treatment decreased the resiquimod-induced glomerular and tubulointerstitial inflammation and attenuated LYVE-1 (+) lymphatic vessel expression in the murine lupus model. Treatment SAR131675 decreased the resiquimod-induced increase of proinflammatory cytokines and chemokines by regulating TLR7/MyD88/IFN-α expression. This study suggests the therapeutic potential of targeting lymphatic proliferation by VEGFR-3 inhibition in lupus nephritis. Modulation of the lymphatic network may provide a novel approach to treating chronic inflammation and attenuating renal autoimmune response.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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