全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

基于转录组测序探讨枸杞多糖调控巨噬细胞极化的机制
Molecular Mechanism of Lycium barbarum Polysaccharides Regulating Macrophage Polarization Based on Transcriptome Sequencing

DOI: 10.12677/hjbm.2026.163047, PP. 442-454

Keywords: 炎症性疾病,巨噬细胞极化,枸杞多糖,转录组测序
Inflammatory Diseases
, Macrophage Polarization, Lycium barbarum Polysaccharides, Transcriptome Sequencing

Full-Text   Cite this paper   Add to My Lib

Abstract:

目的:利用转录组测序技术(RNA-seq)探讨预防性使用枸杞多糖是否影响巨噬细胞的极化状态并探讨其可能的作用机制。方法:用佛波酯(PMA)诱导THP-1细胞使其分化为巨噬细胞样细胞(PMA组);在PMA处理细胞48 h后,利用LPS和IFN-γ将细胞诱导为M1型巨噬细胞(PLI组);在PMA处理细胞48 h后,利用枸杞多糖处理细胞24 h,再利用LPS和IFN-γ将细胞诱导为M1型巨噬细胞(PLLI组)。对三组细胞进行转录组测序筛选差异表达基因,并通过Gene ontology (GO)、京都基因与基因组百科全书(Kyoto Encyclopedia of Genes and Genomes, KEGG)等数据库分析,筛选出差异表达基因富集的相关信号通路,最后用Western blot对分析结果进行验证。结果:经过比较分析发现,与PMA组细胞相比,PLI组细胞中有2760个基因表达上调,3290个基因表达下调;而PLLI组与PLI组相比,则显示262个基因表达上调,288个基因表达下调。值得注意的是,134个基因表现出动态的变化模式:在PLI组相对于PMA组表达升高,却在PLLI组相对于PLI组表达降低,这一特殊调控模式的基因包括ZBP1、HSPD1P6和CCL19等,其中,CCL19是NF-κB信号通路的关键趋化因子。进一步的Western blot实验证实,LBPs处理能够显著下调促炎型标志基因iNOS以及NF-κB信号通路关键蛋白和CCL19的表达水平,同时上调抑炎型巨噬细胞标志基因Arg-1和CD163的表达。结论:预防性使用枸杞多糖可抑制NF-κB信号通路,从而阻碍巨噬细胞向促炎性表型极化。
Objective: RNA-seq technology was employed to investigate whether the preventive use of Lycium barbarum polysaccharides (LBPs) influences the polarization state of macrophages and to preliminarily explore its potential mechanism of action. Method: THP-1 cells were induced to differentiate into macrophage-like cells using phorbol myristate acetate (PMA) (PMA group). After 48 hours of PMA treatment, the cells were polarized into M1-type macrophages using LPS and IFN-γ (PLI group). After 48 hours of PMA treatment, the cells were treated with LBPs for 24 hours before being induced into M1-type macrophages with LPS and IFN-γ (PLLI group). Transcriptome sequencing was performed on the three groups of cells to identify differentially expressed genes (DEGs). These DEGs were subsequently analyzed using databases such as Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) to identify relevant signaling pathways. Finally, the results were validated using Western blot analysis. Results: Comparative analysis revealed that, compared to the PMA group, 2760 genes were upregulated and 3290 were downregulated in the PLI group. In the comparison between the PLLI group and the PLI group, 262 genes were upregulated and 288 were downregulated. Notably, 134 genes exhibited a dynamic expression pattern: their expression increased in the PLI group compared to the PMA group but decreased in the PLLI group compared to the PLI group. Genes with this regulatory pattern included ZBP1, HSPD1P6, and CCL19, among which CCL19 is a key chemokine in the NF-κB signaling

References

[1]  Dinarello, C.A. (2010) Anti-Inflammatory Agents: Present and Future. Cell, 140, 935-950.
https://doi.org/10.1016/j.cell.2010.02.043
[2]  Hirayama, D., Iida, T. and Nakase, H. (2017) The Phagocytic Function of Macrophage-Enforcing Innate Immunity and Tissue Homeostasis. International Journal of Molecular Sciences, 19, Article 92.
https://doi.org/10.3390/ijms19010092
[3]  Li, R., Liu, K., Huang, X., Li, D., Ding, J., Liu, B., et al. (2022) Bioactive Materials Promote Wound Healing through Modulation of Cell Behaviors. Advanced Science, 9, Article ID: 2105152.
https://doi.org/10.1002/advs.202105152
[4]  Zhao, X., Di, Q., Liu, H., Quan, J., Ling, J., Zhao, Z., et al. (2022) MEF2C Promotes M1 Macrophage Polarization and Th1 Responses. Cellular & Molecular Immunology, 19, 540-553.
https://doi.org/10.1038/s41423-022-00841-w
[5]  Zhu, S., Li, X., Dang, B., Wu, F., Wang, C. and Lin, C. (2022) Lycium barbarum Polysaccharide Protects HaCaT Cells from PM2.5-Induced Apoptosis via Inhibiting Oxidative Stress, ER Stress and Autophagy. Redox Report, 27, 32-44.
https://doi.org/10.1080/13510002.2022.2036507
[6]  Wang, J., Gao, H., Xie, Y., Wang, P., Li, Y., Zhao, J., et al. (2023) Lycium barbarum Polysaccharide Alleviates Dextran Sodium Sulfate-Induced Inflammatory Bowel Disease by Regulating M1/M2 Macrophage Polarization via the STAT1 and STAT6 Pathways. Frontiers in Pharmacology, 14, Article 1044576.
https://doi.org/10.3389/fphar.2023.1044576
[7]  Ni, J., Au, M., Kong, H., Wang, X. and Wen, C. (2021) Lycium barbarum Polysaccharides in Ageing and Its Potential Use for Prevention and Treatment of Osteoarthritis: A Systematic Review. BMC Complementary Medicine and Therapies, 21, Article No. 212.
https://doi.org/10.1186/s12906-021-03385-0
[8]  Scherlinger, M., Richez, C., Tsokos, G.C., Boilard, E. and Blanco, P. (2023) The Role of Platelets in Immune-Mediated Inflammatory Diseases. Nature Reviews Immunology, 23, 495-510.
https://doi.org/10.1038/s41577-023-00834-4
[9]  Scherlinger, M., Mertz, P., Sagez, F., Meyer, A., Felten, R., Chatelus, E., et al. (2020) Worldwide Trends in All-Cause Mortality of Auto-Immune Systemic Diseases between 2001 and 2014. Autoimmunity Reviews, 19, Article ID: 102531.
https://doi.org/10.1016/j.autrev.2020.102531
[10]  Broen, J.C.A. and van Laar, J.M. (2020) Mycophenolate Mofetil, Azathioprine and Tacrolimus: Mechanisms in Rheumatology. Nature Reviews Rheumatology, 16, 167-178.
https://doi.org/10.1038/s41584-020-0374-8
[11]  Boutilier, A.J. and Elsawa, S.F. (2021) Macrophage Polarization States in the Tumor Microenvironment. International Journal of Molecular Sciences, 22, Article 6995.
https://doi.org/10.3390/ijms22136995
[12]  Gordon, S. and Martinez, F.O. (2010) Alternative Activation of Macrophages: Mechanism and Functions. Immunity, 32, 593-604.
https://doi.org/10.1016/j.immuni.2010.05.007
[13]  Sica, A. and Mantovani, A. (2012) Macrophage Plasticity and Polarization: In Vivo Veritas. Journal of Clinical Investigation, 122, 787-795.
https://doi.org/10.1172/jci59643
[14]  Li, C., Liu, C., Zhang, J., Lu, Y., Jiang, B., Xiong, H., et al. (2023) Pyruvate Dehydrogenase Kinase Regulates Macrophage Polarization in Metabolic and Inflammatory Diseases. Frontiers in Immunology, 14, Article 1296687.
https://doi.org/10.3389/fimmu.2023.1296687
[15]  Luo, M., Zhao, F., Cheng, H., Su, M. and Wang, Y. (2024) Macrophage Polarization: An Important Role in Inflammatory Diseases. Frontiers in Immunology, 15, Article 1352946.
https://doi.org/10.3389/fimmu.2024.1352946
[16]  Jiao, H., Wachsmuth, L., Kumari, S., Schwarzer, R., Lin, J., Eren, R.O., et al. (2020) Z-Nucleic-Acid Sensing Triggers ZBP1-Dependent Necroptosis and Inflammation. Nature, 580, 391-395.
https://doi.org/10.1038/s41586-020-2129-8
[17]  Koerner, L., Wachsmuth, L., Kumari, S., Schwarzer, R., Wagner, T., Jiao, H., et al. (2024) ZBP1 Causes Inflammation by Inducing RIPK3-Mediated Necroptosis and RIPK1 Kinase Activity-Independent Apoptosis. Cell Death & Differentiation, 31, 938-953.
https://doi.org/10.1038/s41418-024-01321-6
[18]  Liu, R., Cao, H., Zhang, S., Cai, M., Zou, T., Wang, G., et al. (2024) ZBP1-Mediated Apoptosis and Inflammation Exacerbate Steatotic Liver Ischemia/Reperfusion Injury. Journal of Clinical Investigation, 134, e180451.
https://doi.org/10.1172/jci180451
[19]  Yokosawa, T., Miyagawa, S., Suzuki, W., Nada, Y., Hirata, Y., Noguchi, T., et al. (2024) The E3 Ubiquitin Protein Ligase LINCR Amplifies the TLR-Mediated Signals through Direct Degradation of Mkp1. Cells, 13, Article 687.
https://doi.org/10.3390/cells13080687
[20]  Nakano, K., Whitehead, G.S., Lyons-Cohen, M.R., Grimm, S.A., Wilkinson, C.L., Izumi, G., et al. (2024) Chemokine CCL19 Promotes Type 2 T-Cell Differentiation and Allergic Airway Inflammation. Journal of Allergy and Clinical Immunology, 153, 487-502.e9.
https://doi.org/10.1016/j.jaci.2023.10.024
[21]  Damås, J.K., Landrø, L., Fevang, B., Heggelund, L., Tjønnfjord, G.E., Fløisand, Y., et al. (2009) Homeostatic Chemokines CCL19 and CCL21 Promote Inflammation in Human Immunodeficiency Virus-Infected Patients with Ongoing Viral Replication. Clinical and Experimental Immunology, 157, 400-407.
https://doi.org/10.1111/j.1365-2249.2009.03976.x
[22]  Yamashita, N., Tashimo, H., Matsuo, Y., Ishida, H., Yoshiura, K., Sato, K., et al. (2006) Role of CCL21 and CCL19 in Allergic Inflammation in the Ovalbumin-Specific Murine Asthmatic Model. Journal of Allergy and Clinical Immunology, 117, 1040-1046.
https://doi.org/10.1016/j.jaci.2006.01.009
[23]  Zhao, Y., Hasse, S., Vaillancourt, M., Zhao, C., Davis, L., Boilard, E., et al. (2021) Phospholipase A1 Member a Activates Fibroblast-Like Synoviocytes through the Autotaxin-Lysophosphatidic Acid Receptor Axis. International Journal of Molecular Sciences, 22, Article 12685.
https://doi.org/10.3390/ijms222312685
[24]  Zhao, J., Wang, Y., Wu, X., Tong, P., Yue, Y., Gao, S., et al. (2018) Inhibition of CCL19 Benefits Non-Alcoholic Fatty Liver Disease by Inhibiting TLR4/NF-κB-p65 Signaling. Molecular Medicine Reports, 18, 4635-4642.
https://doi.org/10.3892/mmr.2018.9490
[25]  Tourniaire, F., Romier-Crouzet, B., Lee, J.H., Marcotorchino, J., Gouranton, E., Salles, J., et al. (2013) Chemokine Expression in Inflamed Adipose Tissue Is Mainly Mediated by NF-κB. PLoS ONE, 8, e66515.
https://doi.org/10.1371/journal.pone.0066515
[26]  Chen, M., Reed, R.R. and Lane, A.P. (2019) Chronic Inflammation Directs an Olfactory Stem Cell Functional Switch from Neuroregeneration to Immune Defense. Cell Stem Cell, 25, 501-513.e5.
https://doi.org/10.1016/j.stem.2019.08.011

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133