Bhusal Anup, Kim Jae-Hong, Kim Seung-Chan, Hwang Eun Mi, Ryu Hoon, Ali Md Sekendar, Park Seung-Chun, Lee Won-Ha, Suk Kyoungho
Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea; BK21 Plus KNU Biomedical Convergence Program, Department of Biomedical Science, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.
Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea; Brain Korea 21 Four KNU Convergence Educational Program of Biomedical Sciences for Creative Future Talents, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.
Cell Rep. 2024 Mar 26;43(3):113813. doi: 10.1016/j.celrep.2024.113813. Epub 2024 Feb 22.
Peptidoglycan recognition protein 1 (PGLYRP1) is a pattern-recognition protein that mediates antibacterial actions and innate immune responses. Its expression and role in neuroinflammatory conditions remain unclear. We observed the upregulation of PGLYRP1 in inflamed human and mouse spinal cord and brain, with microglia being the primary cellular source. Experiments using a recombinant PGLYRP1 protein show that PGLYRP1 potentiates reactive gliosis, neuroinflammation, and consequent behavioral changes in multiple animal models of neuroinflammation. Furthermore, shRNA-mediated knockdown of Pglyrp1 gene expression attenuates this inflammatory response. In addition, we identify triggering receptor expressed on myeloid cell-1 (TREM1) as an interaction partner of PGLYRP1 and demonstrate that PGLYRP1 promotes neuroinflammation through the TREM1-Syk-Erk1/2-Stat3 axis in cultured glial cells. Taken together, our results reveal a role for microglial PGLYRP1 as a neuroinflammation mediator. Finally, we propose that PGLYRP1 is a potential biomarker and therapeutic target in various neuroinflammatory diseases.
肽聚糖识别蛋白1(PGLYRP1)是一种模式识别蛋白,可介导抗菌作用和先天免疫反应。其在神经炎症性疾病中的表达及作用尚不清楚。我们观察到在人类和小鼠发炎的脊髓和大脑中PGLYRP1上调,小胶质细胞是主要的细胞来源。使用重组PGLYRP1蛋白进行的实验表明,PGLYRP1在多种神经炎症动物模型中增强了反应性胶质增生、神经炎症以及随之而来的行为变化。此外,shRNA介导的Pglyrp1基因表达敲低减弱了这种炎症反应。另外,我们确定髓系细胞触发受体1(TREM1)为PGLYRP1的相互作用伙伴,并证明PGLYRP1在培养的胶质细胞中通过TREM1-Syk-Erk1/2-Stat3轴促进神经炎症。综上所述,我们的结果揭示了小胶质细胞PGLYRP1作为神经炎症介质的作用。最后,我们提出PGLYRP1是各种神经炎症性疾病的潜在生物标志物和治疗靶点。
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