Expression and Significance of SLAMF7 in Intestinal Tissue and Intestinal Inflammation in Mice
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摘要: 目的 探讨细胞表面受体信号淋巴细胞活化分子受体7(signaling lymphocytic activation molecule receptor family 7,SLAMF7)在小鼠正常肠道组织和肠道炎症组织中的表达及意义。 方法 选择8~10周龄C57BL/6J野生型(wild-type,WT)雄性小鼠5只,正常饮用水喂养,提取其结肠固有层淋巴细胞(lamina propria lymphocytes,LPLs)和肠上皮细胞(intestinal epithelial cells,IECs),Trizol试剂提取细胞总RNA,逆转录聚合酶链式反应(reverse transcription polymerase chain reaction,RT-PCR)和实时荧光定量聚合酶链式反应(real-time fluorescence quantitative polymerase chain reaction,RT-qPCR)检测细胞中SLAMF7的mRNA表达情况。选择8~10周龄C57BL/6J野生型(wild-type,WT)雄性小鼠10只,随机分为对照组和模型组,每组各5只。对照组用正常饮用水喂养5 d;模型组用含2.5%葡聚糖硫酸酯钠盐(dextran sodium sulfate,DSS)的饮用水喂养5 d,建立小鼠溃疡性结肠炎(ulcerative colitis,UC)模型。第5天处死两组小鼠,采用流式细胞术检测对照组与模型组SLAMF7在免疫细胞亚群中的表达情况。 结果 相较于结肠IECs,SLAMF7在结肠LPLs中表达较高(P=0.017); DSS诱导肠炎后,SLAMF7在中性粒细胞中的表达上调(P=0.001),在CD4+T细胞、CD8+T细胞、B细胞、巨噬细胞、经典树突状细胞(conventional dendritic cell,cDC)中的表达无明显变化(P均>0.05)。 结论 SLAMF7可能通过中性粒细胞相关途径在UC的发生发展过程中发挥重要作用。Abstract: Objective To investigate the expression and significance of cell surface receptor signaling lymphocyte activation molecule receptor 7 (SLAMF7) in normal intestinal tissues and intestinal inflammatory tissues of mice. Methods Five C57BL/6J wild-type male mice aged 8-10 weeks were taken and fed normally. Lamina propria lymphocytes (LPLs) and intestinal epithelial cells (IECs) were extracted, and total cell RNA was extracted by Trizol reagent. The mRNA expression of SLAMF7 in cells was detected by reverse transcription polymerase chain reaction (RT-PCR) and real-time fluorescent quantitative polymerase chain reaction (RT-qPCR). Ten C57BL/6J wild-type male mice aged 8-10 weeks were randomly divided into control group (n=5) and model group (n=5). The control group was fed with normal drinking water for 5 days, the model group was fed with 2.5% dextran sodium sulfate (DSS) drinking water for 5 days to establish a model of ulcerative colitis(UC), and the mice in both groups were killed on the 5th day. Flow cytometry was used to detect the expression of SLAMF7 in immune cell subpopulations in the control group and the model group. Results Compared with colonic IECs, the expression of SLAMF7 was higher in colonic LPLs (P=0.017). After DSS induced enteritis, the expression of SLAMF7 was up-regulated in neutrophils (P=0.001), but had no significant changes in CD4+T cells, CD8+T cells, B cells, macrophages and conventional dendritic cell (all P>0.05). Conclusion SLAMF7 may play a certain role in the occurrence and development of UC through neutrophilrelated pathways.
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Key words:
- Inflammatory bowel diseases /
- Ulcerative colitis /
- Lamina propria lymphocytes /
- SLAMF7
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[1] Lamb C A, Kennedy N A, Raine T, et al. British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults [J]. Gut, 2019, 68(Suppl 3): s1-s106. [2] Feuerstein J D, Moss A C, Farraye F A. Ulcerative Colitis [J]. Mayo Clin Proc, 2019, 94(7): 1357-1373. [3] 刘峰, 刘林, 王垂杰. 溃疡性结肠炎病因病机及治疗进展[J]. 山东中医药大学学报, 2021, 45: 143-147. [4] Le Berre C, Honap S, Peyrin-Biroulet L. Ulcerative colitis [J]. Lancet, 2023, 402(10401): 571-584. [5] Calpe S, Wang N, Romero X, et al. The SLAM and SAP gene families control innate and adaptive immune responses [J]. Adv Immunol, 2008, 97: 177-250. [6] Cannons J L, Tangye S G, Schwartzberg P L. SLAM family receptors and SAP adaptors in immunity [J]. Annu Rev Immunol, 2011, 29: 665-705. [7] Bouchon A, Cella M, Grierson H L, et al. Activation of NK cell-mediated cytotoxicity by a SAPindependent receptor of the CD2 family [J]. J Immunol, 2001, 167(10): 5517-5521. [8] Tai Y T, Dillon M, Song W, et al. Anti-CS1 humanized monoclonal antibody HuLuc63 inhibits myeloma cell adhesion and induces antibody-dependent cellular cytotoxicity in the bone marrow milieu [J]. Blood, 2008, 112(4): 1329-1337. [9] Lee J L, Roh S A, Kim C W, et al. Clinical assessment and identification of immuno-oncology markers concerning the 19-gene based risk classifier in stage IV colorectal cancer [J]. World J Gastroenterol, 2019, 25(11): 1341-1354. [10] Wu Y, Wang Q, Li M, et al. SLAMF7 regulates the inflammatory response in macrophages during polymicrobial sepsis [J]. J Clin Invest, 2023, 133(6). [11] 康萍, 蒋茜, 毛朝明, 等. SLAMF7在大颗粒淋巴细胞白血病患者外周血淋巴细胞中的表达及意义 [J]. 山东医药, 2020, 60: 76-79. [12] O'Connell P, Blake M K, Godbehere S, et al. SLAMF7 modulates B cells and adaptive immunity to regulate susceptibility to CNS autoimmunity [J]. J Neuroinflammation, 2022, 19(1): 241. [13] 赵珊, 王鹏程, 王秋红, 等. 小鼠葡聚糖硫酸钠急性溃疡性结肠炎模型的建立和评价[J]. 辽宁中医药大学学报, 2016, 18: 42-45. [14] Chen J, Zhong M C, Guo H, et al. SLAMF7 is critical for phagocytosis of haematopoietic tumour cells via Mac-1 integrin [J]. Nature, 2017, 544(7651): 493-497. [15] Kim J R, Horton N C, Mathew S O, et al. CS1(SLAMF7) inhibits production of proinflammatory cytokines by activated monocytes [J]. Inflamm Res, 2013, 62(8): 765-772. [16] Kaplan G G. The global burden of IBD: from 2015 to 2025[J]. Nat Rev Gastroenterol Hepatol, 2015, 12(12): 720-727. [17] Brazil J C, Louis N A, Parkos C A. The role of polymorphonuclear leukocyte trafficking in the perpetuation of inflammation during inflammatory bowel disease [J]. Inflamm Bowel Dis, 2013, 19(7): 1556-1565. [18] Dinallo V, Marafini I, Di Fusco D, et al. Neutrophil Extracellular Traps Sustain Inflammatory Signals in Ulcerative Colitis [J]. Journal of Crohn's and Colitis, 2019, 13(6): 772-784. [19] Wang Z, Li S, Cao Y, et al. Oxidative Stress and Carbonyl Lesions in Ulcerative Colitis and Associated Colorectal Cancer [J]. Oxid Med Cell Longev, 2016, 2016: 9875298. [20] Muthas D, Reznichenko A, Balendran C A, et al. Neutrophils in ulcerative colitis: a review of selected biomarkers and their potential therapeutic implications [J]. Scand J Gastroenterol, 2017, 52(2): 125-135. [21] Yan X, Meng L, Zhang X, et al. Reactive oxygen species-responsive nanocarrier ameliorates murine colitis by intervening colonic innate and adaptive immune responses [J]. Mol Ther, 2023, 31(5): 1383-1401. [22] Kaluzna A, Olczyk P, Komosinska-Vassev K. The Role of Innate and Adaptive Immune Cells in the Pathogenesis and Development of the Inflammatory Response in Ulcerative Colitis [J]. J Clin Med, 2022, 11(2). [23] Dong W, Liu D, Zhang T, et al. Oral delivery of staphylococcal nuclease ameliorates DSS induced ulcerative colitis in mice via degrading intestinal neutrophil extracellular traps [J]. Ecotoxicol Environ Saf, 2021, 215: 112161. [24] Lin E Y, Lai H J, Cheng Y K, et al. Neutrophil Extracellular Traps Impair Intestinal Barrier Function during Experimental Colitis [J]. Biomedicines, 2020, 8(8). [25] Curciarello R, Sobande T, Jones S, et al. Human Neutrophil Elastase Proteolytic Activity in Ulcerative Colitis Favors the Loss of Function of Therapeutic Monoclonal Antibodies [J]. J Inflamm Res, 2020, 13: 233-243. [26] Kamekura R, Nava P, Feng M, et al. Inflammation-induced desmoglein-2 ectodomain shedding compromises the mucosal barrier [J]. Mol Biol Cell, 2015, 26(18): 3165-3177. [27] Sandborn W J, Bhandari B R, Randall C, et al. Andecaliximab [Anti-matrix Metalloproteinase-9] Induction Therapy for Ulcerative Colitis: A Randomised, Double-Blind, Placebo-Controlled, Phase 2/3 Study in Patients With Moderate to Severe Disease [J]. J Crohns Colitis, 2018, 12(9): 1021-1029. [28] Gideon H P, Phuah J, Junecko B A, et al. Neutrophils express pro-and anti-inflammatory cytokines in granulomas from Mycobacterium tuberculosis-infected cynomolgus macaques [J]. Mucosal Immunol, 2019, 12(6): 1370-1381. [29] Li Y, Zhang Y Y, Yang L T, et al. FcγRI plays a critical role in patients with ulcerative colitis relapse [J]. Eur J Immunol, 2021, 51(2): 459-470. [30] Chen H, Wu X, Xu C, et al. Dichotomous roles of neutrophils in modulating pathogenic and repair processes of inflammatory bowel diseases [J]. Precis Clin Med, 2021, 4(4): 246-257.
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