Kempuraj Duraisamy, Tsilioni Irene, Aenlle Kristina K, Klimas Nancy G, Theoharides Theoharis C
Institute for Neuro-Immune Medicine (INIM), Dr. Kiran C. Patel College of Osteopathic Medicine, Nova Southeastern University, Ft. Lauderdale, FL, 33328, United States of America.
Laboratory of Molecular Immunopharmacology and Drug Discovery, Department of Immunology, Tufts University School of Medicine, Boston, MA, 02111, United States of America.
Transl Neurosci. 2024 Oct 13;15(1):20220352. doi: 10.1515/tnsci-2022-0352. eCollection 2024 Jan 1.
Long COVID is a major health concern because many patients develop chronic neuropsychiatric symptoms, but the precise pathogenesis is unknown. Matrix metalloproteinase-9 (MMP-9) can disrupt neuronal connectivity and be elevated in patients with long COVID.
In this study, MMP-9 was measured in the serum of long COVID patients and healthy controls, as well as in the supernatant fluid of cultured human microglia cell line stimulated by recombinant severe acute respiratory syndrome coronavirus 2 Spike protein, as well as lipopolysaccharide (LPS) and neurotensin (NT) used as positive controls. MMP-9 was measured by commercial enzyme-linked immunosorbent assay.
MMP-9 was significantly elevated in the serum of long COVID patients compared to healthy controls. Moreover, there was significant release of MMP-9 from a cultured human microglia cell line stimulated by LPS, NT, or Spike protein. We further show that pretreatment with the flavonoids luteolin and tetramethoxyluteolin (methlut) significantly inhibited the release of MMP-9 stimulated by the Spike protein.
MMP-9 from Spike protein-stimulated microglia could contribute to the development of long COVID and may serve as a target for treatment including the use of luteolin.
长期新冠是一个主要的健康问题,因为许多患者会出现慢性神经精神症状,但其确切发病机制尚不清楚。基质金属蛋白酶-9(MMP-9)可破坏神经元连接,且在长期新冠患者中水平升高。
在本研究中,对长期新冠患者和健康对照者的血清进行MMP-9检测,同时检测重组严重急性呼吸综合征冠状病毒2刺突蛋白刺激的人小胶质细胞系培养上清液中的MMP-9,以及用作阳性对照的脂多糖(LPS)和神经降压素(NT)。采用商业酶联免疫吸附测定法检测MMP-9。
与健康对照相比,长期新冠患者血清中的MMP-9显著升高。此外,LPS、NT或刺突蛋白刺激的人小胶质细胞系培养上清液中MMP-9有显著释放。我们进一步表明,用黄酮类化合物木犀草素和四甲氧基木犀草素(甲氧基木犀草素)预处理可显著抑制刺突蛋白刺激的MMP-9释放。
刺突蛋白刺激的小胶质细胞产生的MMP-9可能促使长期新冠的发展,并且可能成为包括使用木犀草素在内的治疗靶点。