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在患有脊椎关节炎的患者中,经典型单核细胞中 VEGFA-mRNA 的表达和非经典型单核细胞中 MSX2-mRNA 的表达与外周关节炎相关。

Expression of VEGFA-mRNA in classical and MSX2-mRNA in non-classical monocytes in patients with spondyloarthritis is associated with peripheral arthritis.

机构信息

Department of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, Wielicka 265 Str., 30-663, Kraków, Poland.

Center for Medical Genomics OMICRON, Jagiellonian University Medical College, Kopernika 7c Str., 31-034, Kraków, Poland.

出版信息

Sci Rep. 2021 May 6;11(1):9693. doi: 10.1038/s41598-021-89037-2.

Abstract

Spondyloarthritis (SpA) is characterized by chronic inflammation and structural damage involving spine and peripheral joints. Monocytes, as part of innate immune system, following migration into affected tissue, may play a role in the pathogenesis of SpA. Here, potential associations between osteogenesis-linked gene expression profile in particular monocyte subpopulations and clinical signs of SpA were investigated. The 20 patients with axial and 16 with peripheral SpA were enrolled in the study. Monocyte subpopulations (classical-CD14CD16, intermediate-CD14CD16 and non-classical-CD14CD16) were isolated from blood using flow cytometry and gene expression analysis was performed using real-time PCR method and TaqMan Array, Human Osteogenesis, Fast 96-well plates. Next, the characteristic clinical features shared by axial and peripheral SpA were analyzed in the context of the expression of selected genes in the three subpopulations of monocytes. We demonstrated that expression of VEGFA in classical and MSX2 in non-classical monocytes were associated with the number of swollen and painful peripheral joints of SpA patients. We conclude that monocytes may contribute to the development of peripheral arthritis in SpA patients. This might be possible through subpopulation specific effects, linking number of inflamed joints with expression of VEGFA in classical monocytes and MSX2 in non-classical monocytes.

摘要

脊柱关节炎(SpA)的特征是慢性炎症和涉及脊柱和外周关节的结构损伤。单核细胞作为固有免疫系统的一部分,在迁移到受影响的组织后,可能在 SpA 的发病机制中发挥作用。在这里,研究了特定单核细胞亚群中的骨生成相关基因表达谱与 SpA 的临床体征之间的潜在关联。20 例轴性 SpA 患者和 16 例外周 SpA 患者入组本研究。使用流式细胞术从血液中分离单核细胞亚群(经典-CD14CD16、中间-CD14CD16 和非经典-CD14CD16),并使用实时 PCR 方法和 TaqMan 阵列、人类成骨术、快速 96 孔板进行基因表达分析。接下来,根据单核细胞三个亚群中选定基因的表达,分析了轴性和外周性 SpA 的特征性临床特征。我们证明,经典单核细胞中 VEGFA 的表达和非经典单核细胞中 MSX2 的表达与 SpA 患者肿胀和疼痛的外周关节数量有关。我们的结论是,单核细胞可能有助于 SpA 患者外周关节炎的发展。这可能是通过亚群特异性的影响来实现的,将炎症关节的数量与经典单核细胞中的 VEGFA 表达和非经典单核细胞中的 MSX2 表达联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36aa/8102490/e86ffbfb51ff/41598_2021_89037_Fig1_HTML.jpg

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