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托法替布通过对 CD147 和组织蛋白酶 S 的作用调节内皮抑素。

Tofacitinib Regulates Endostatin via Effects on CD147 and Cathepsin S.

机构信息

Department of Rheumatology, Carmel Medical Center, Haifa 3436212, Israel.

Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 3525422, Israel.

出版信息

Int J Mol Sci. 2024 Jul 2;25(13):7267. doi: 10.3390/ijms25137267.

Abstract

Angiogenesis is critical for rheumatoid arthritis (RA) progression. The effects of tofacitinib, a JAK-STAT inhibitor used for RA treatment, on angiogenesis in RA are unclear. We, therefore, evaluated the levels of angiogenic factors in two systems of a human co-culture of fibroblast (HT1080) and monocytic (U937) cell lines treated with tofacitinib and in serum samples from RA patients before and after six months of tofacitinib treatment. Tofacitinib reduced CD147 levels, matrix metalloproteinase-9 (MMP-9) activity, and angiogenic potential but increased endostatin levels and secreted proteasome 20S activity. In vitro, tofacitinib did not change CD147 mRNA but increased miR-146a-5p expression and reduced STAT3 phosphorylation. We recently showed that CD147 regulates the ability of MMP-9 and secreted proteasome 20S to cleave collagen XVIIIA into endostatin. We show here that tofacitinib-enhanced endostatin levels are mediated by CD147, as CD147-siRNA or an anti-CD147 antibody blocked proteasome 20S activity. The correlation between CD147 and different disease severity scores supported this role. Lastly, tofacitinib reduced endostatin' s degradation by inhibiting cathepsin S activity and recombinant cathepsin S reversed this in both systems. Thus, tofacitinib inhibits angiogenesis by reducing pro-angiogenic factors and enhancing the anti-angiogenic factor endostatin in a dual effect mediated partly through CD147 and partly through cathepsin S.

摘要

血管生成对于类风湿关节炎(RA)的进展至关重要。JAK-STAT 抑制剂托法替尼用于 RA 治疗,但其对 RA 血管生成的影响尚不清楚。因此,我们评估了在人成纤维细胞(HT1080)和单核细胞(U937)细胞系共培养的两个系统中以及在接受托法替尼治疗 6 个月前后的 RA 患者血清样本中,血管生成因子的水平。托法替尼降低了 CD147 水平、基质金属蛋白酶-9(MMP-9)活性和血管生成潜能,但增加了内皮抑素水平和分泌蛋白酶体 20S 活性。在体外,托法替尼没有改变 CD147 mRNA,但增加了 miR-146a-5p 的表达并减少了 STAT3 磷酸化。我们最近表明,CD147 调节 MMP-9 和分泌蛋白酶体 20S 将胶原 XVIIIA 切割成内皮抑素的能力。我们在这里表明,托法替尼增强的内皮抑素水平是由 CD147 介导的,因为 CD147-siRNA 或抗 CD147 抗体阻断了蛋白酶体 20S 活性。CD147 与不同疾病严重程度评分之间的相关性支持了这一作用。最后,托法替尼通过抑制组织蛋白酶 S 活性来降低内皮抑素的降解,并且重组组织蛋白酶 S 在两个系统中均逆转了这一作用。因此,托法替尼通过降低促血管生成因子并增强抗血管生成因子内皮抑素来抑制血管生成,这种双重作用部分通过 CD147 介导,部分通过组织蛋白酶 S 介导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0828/11241738/e416bbe72234/ijms-25-07267-g001.jpg

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