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使用选择性IκB激酶β抑制剂NEMO结合域肽进行局部治疗可改善滑膜炎症。

Local treatment with the selective IkappaB kinase beta inhibitor NEMO-binding domain peptide ameliorates synovial inflammation.

作者信息

Tas Sander W, Vervoordeldonk Margriet J, Hajji Najat, May Michael J, Ghosh Sankar, Tak Paul P

机构信息

Division of Clinical Immunology and Rheumatology F4-218, Academic Medical Center/University of Amsterdam, PO Box 22700, 1100 DE Amsterdam, The Netherlands.

出版信息

Arthritis Res Ther. 2006;8(4):R86. doi: 10.1186/ar1958.

Abstract

Nuclear factor (NF)-kappaB is a key regulator of synovial inflammation. We investigated the effect of local NF-kappaB inhibition in rat adjuvant arthritis (AA), using the specific IkappaB kinase (IKK)-beta blocking NF-kappaB essential modulator-binding domain (NBD) peptide. The effects of the NBD peptide on human fibroblast-like synoviocytes (FLS) and macrophages, as well as rheumatoid arthritis (RA) whole-tissue biopsies, were also evaluated. First, we investigated the effects of the NBD peptide on RA FLS in vitro. Subsequently, NBD peptides were administered intra-articularly into the right ankle joint of rats at the onset of disease. The severity of arthritis was monitored over time, rats were sacrificed on day 20, and tissue specimens were collected for routine histology and x-rays of the ankle joints. Human macrophages or RA synovial tissues were cultured ex vivo in the presence or absence of NBD peptides, and cytokine production was measured in the supernatant by enzyme-linked immunosorbent assay. The NBD peptide blocked interleukin (IL)-1-beta-induced IkappaB alpha phosphorylation and IL-6 production in RA FLS. Intra-articular injection of the NBD peptide led to significantly reduced severity of arthritis (p < 0.0001) and reduced radiological damage (p = 0.04). This was associated with decreased synovial cellularity and reduced expression of tumor necrosis factor (TNF)-alpha and IL-1-beta in the synovium. Incubation of human macrophages with NBD peptides resulted in 50% inhibition of IL-1-beta-induced TNF-alpha production in the supernatant (p < 0.01). In addition, the NBD peptide decreased TNF-alpha-induced IL-6 production by human RA synovial tissue biopsies by approximately 42% (p < 0.01). Specific NF-kappaB blockade using a small peptide inhibitor of IKK-beta has anti-inflammatory effects in AA and human RA synovial tissue as well as in two important cell types in the pathogenesis of RA: macrophages and FLS. These results indicate that IKK-beta-targeted NF-kappaB blockade using the NBD peptide could offer a new approach for the local treatment of arthritis.

摘要

核因子(NF)-κB是滑膜炎症的关键调节因子。我们使用特异性抑制κB激酶(IKK)-β阻断NF-κB必需调节因子结合域(NBD)肽,研究了局部抑制NF-κB在大鼠佐剂性关节炎(AA)中的作用。还评估了NBD肽对人成纤维细胞样滑膜细胞(FLS)、巨噬细胞以及类风湿关节炎(RA)全组织活检的影响。首先,我们在体外研究了NBD肽对RA FLS的影响。随后,在疾病发作时将NBD肽关节内注射到大鼠的右踝关节。随时间监测关节炎的严重程度,在第20天处死大鼠,并收集组织标本用于踝关节的常规组织学检查和X线检查。在有或没有NBD肽的情况下对人巨噬细胞或RA滑膜组织进行离体培养,并通过酶联免疫吸附测定法测量上清液中的细胞因子产生。NBD肽可阻断白细胞介素(IL)-1-β诱导的RA FLS中IκBα磷酸化和IL-6产生。关节内注射NBD肽可导致关节炎严重程度显著降低(p<0.0001)和放射学损伤减轻(p = 0.04)。这与滑膜细胞数量减少以及滑膜中肿瘤坏死因子(TNF)-α和IL-1-β表达降低有关。用NBD肽孵育人巨噬细胞导致上清液中IL-1-β诱导的TNF-α产生受到50%的抑制(p<0.01)。此外,NBD肽使TNF-α诱导的人RA滑膜组织活检中的IL-6产生减少约42%(p<0.01)。使用IKK-β的小肽抑制剂进行特异性NF-κB阻断在AA和人RA滑膜组织以及RA发病机制中的两种重要细胞类型:巨噬细胞和FLS中具有抗炎作用。这些结果表明,使用NBD肽靶向IKK-β的NF-κB阻断可为关节炎的局部治疗提供一种新方法。

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