Laboratorio PABIOM, Facultad de Medicina y Ciencias Biomédicas, Universidad Autónoma de Chihuahua, Chihuahua 31125, Mexico.
Radiology Department, Memorial Sloan Kettering Cancer Center, 1275 York Ave, New York, NY 10065, USA.
Cells. 2023 Mar 8;12(6):842. doi: 10.3390/cells12060842.
The fibroblast-like synoviocytes (FLS) have a crucial role in the pathogenesis of Rheumatoid Arthritis (RA); however, its precise mechanisms remain partially unknown. The involvement of the fibroblast in activating adjuvant-induced arthritis (AA) has not been previously reported. The objective was to describe the participation of footpads' fibroblasts in the critical initial process that drives the AA onset. Wistar rats were injected with Complete Freund's Adjuvant (CFA) or saline solution in the hind paws' footpads and euthanized at 24 or 48 h for genetic and histological analyses. Microarrays revealed the differentially expressed genes between the groups. The CFA dysregulated RA-linked biological processes at both times. Genes of MAPK, Jak-STAT, HIF, PI3K-Akt, TLR, TNF, and NF-κB signaling pathways were altered 24 h before the arrival of immune cells (CD4, CD8, and CD68). Key markers TNF-α, IL-1β, IL-6, NFκB, MEK-1, JAK3, Enolase, and VEGF were immunodetected in fibroblast in CFA-injected footpads at 24 h but not in the control group. Moreover, fibroblasts in the CFA inoculation site overexpressed cadherin-11, which is linked to the migration and invasion ability of RA-FLS. Our study shows that CFA induced a pathological phenotype in the fibroblast of the inoculation site at very early AA stages from 24 h, suggesting a prominent role in arthritis activation processes.
成纤维样滑膜细胞(FLS)在类风湿关节炎(RA)的发病机制中起着至关重要的作用;然而,其确切的机制仍部分未知。成纤维细胞在激活佐剂诱导的关节炎(AA)中的作用尚未被报道。本研究旨在描述足底成纤维细胞在驱动 AA 发病的关键初始过程中的参与作用。将 Wistar 大鼠的后脚掌皮内注射完全弗氏佐剂(CFA)或生理盐水,并在 24 或 48 小时处死,进行基因和组织学分析。微阵列分析显示了两组之间差异表达的基因。CFA 在两个时间点均失调了 RA 相关的生物学过程。MAPK、Jak-STAT、HIF、PI3K-Akt、TLR、TNF 和 NF-κB 信号通路的基因在免疫细胞(CD4、CD8 和 CD68)到达前 24 小时就发生了改变。在 CFA 注射的足底成纤维细胞中,24 小时时可检测到 TNF-α、IL-1β、IL-6、NFκB、MEK-1、JAK3、烯醇酶和 VEGF 等关键标记物,但在对照组中则没有。此外,CFA 接种部位的成纤维细胞过表达了钙黏蛋白-11,该蛋白与 RA-FLS 的迁移和侵袭能力有关。本研究表明,CFA 在非常早期的 AA 阶段(24 小时)就诱导了接种部位成纤维细胞的病理表型,提示其在关节炎激活过程中具有重要作用。