Rithvik Arulkumaran, Bhattacharjee Shangomitra, Gupta Manshi Kumari, Sudandiradoss C, Wadud Abdul, Rasool Mahaboobkhan
Immunopathology Lab, School of Biosciences and Technology, Vellore Institute of Technology (VIT), Vellore, Tamil Nadu, India.
Department of Biotechnology, School of Biosciences and Technology, Vellore Institute of Technology (VIT), Vellore, Tamil Nadu, India.
Front Immunol. 2025 Aug 29;16:1633061. doi: 10.3389/fimmu.2025.1633061. eCollection 2025.
The acquired tumorigenic phenotype of the resident fibroblast like synoviocytes (FLS) is cornerstone to exacerbating rheumatoid arthritis (RA) disease progression. Toll like receptor 4 (TLR4) signalling can sustain the proliferative and invasive phenotype of these synoviocytes resulting in cartilage degradation and bone damage. A marked increase in glycolytic activity also contributes to the malignant character of these cells. Herein, we aim to study the prospects of TLR4 activation leading to improved glycolytic flux. Further, we also strategize the therapeutic modality of Habbe Gule Aakh (HGA), a polyherbal unani formulation to rescue disease progression via blockade of TLR4 activation.
We activated TLR4 signaling in SW982 cells, cultured in high glucose medium. Initially, the expression profile of glycolytic rate limiting enzymes- hexokinase 2 (HK2) and pyruvate kinase M2 (PKM2) was assessed. Next, we evaluated the ability of HGA to regulate the expression of these enzymes via ablation of TLR4 activation. Further, we investigated the pathway of glucose uptake via tissue inhibitor of matrix metalloproteinase 1 or TIMP1 and counterintuitively investigated HGA to arrest the uptake of glucose via p65-TIMP1 signaling axis. To sufficiently validate our findings, we utilised network pharmacology approach, to uncover the interactome of HGA against rheumatoid arthritis targets. Ultimately, we leveraged in-vivo models to support the anti-arthritic claims of HGA.
HGA regulated the proliferation and invasive phenotype of SW982 cells cultured in high glucose medium via blockade of TLR4 activation. Further, in-silico and in-vivo approaches suggest a mechanistic insight to the anti-arthritic activity of HGA upon blockade of TLR4-mediated glycolytic flux in resident synoviocytes.
Pharmacological intervention with Habbe Gule Aakh can rescue exacerbation of rheumatoid arthritis disease severity via TLR4 signaling axis. The findings of this study strengthen the rationale for the use of HGA in clinical settings involving RA patients.
驻留的成纤维样滑膜细胞(FLS)获得的致瘤表型是加剧类风湿性关节炎(RA)疾病进展的基石。Toll样受体4(TLR4)信号传导可维持这些滑膜细胞的增殖和侵袭表型,导致软骨降解和骨损伤。糖酵解活性的显著增加也促成了这些细胞的恶性特征。在此,我们旨在研究TLR4激活导致糖酵解通量改善的前景。此外,我们还制定了Habbe Gule Aakh(HGA)的治疗方案,这是一种多草药尤那尼配方,通过阻断TLR4激活来挽救疾病进展。
我们在高糖培养基中培养的SW982细胞中激活TLR4信号传导。首先,评估糖酵解限速酶己糖激酶2(HK2)和丙酮酸激酶M2(PKM2)的表达谱。接下来,我们评估了HGA通过消除TLR4激活来调节这些酶表达的能力。此外,我们研究了通过基质金属蛋白酶1组织抑制剂或TIMP1的葡萄糖摄取途径,并且出乎意料地研究了HGA通过p65-TIMP1信号轴阻止葡萄糖摄取的情况。为了充分验证我们的发现,我们利用网络药理学方法来揭示HGA针对类风湿性关节炎靶点的相互作用组。最终,我们利用体内模型来支持HGA的抗关节炎作用。
HGA通过阻断TLR4激活来调节在高糖培养基中培养的SW^982细胞的增殖和侵袭表型。此外,计算机模拟和体内方法表明,在阻断驻留滑膜细胞中TLR4介导的糖酵解通量后,对HGA的抗关节炎活性有了机制上的深入了解。
用Habbe Gule Aakh进行药物干预可以通过TLR4信号轴挽救类风湿性关节炎疾病严重程度的加剧。本研究结果加强了在涉及RA患者的临床环境中使用HGA的理论依据。