[1]方伟华,庄至坤,彭鹏,等.激素性股骨头坏死滑膜病变分子机制的实验研究[J].中医正骨,2024,36(09):49-58,75.
 FANG Weihua,ZHUANG Zhikun,PENG Peng,et al.Molecular mechanisms of synovial lesions in steroid-induced osteonecrosis of the femoral head:an experimental study[J].The Journal of Traditional Chinese Orthopedics and Traumatology,2024,36(09):49-58,75.
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激素性股骨头坏死滑膜病变分子机制的实验研究()
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《中医正骨》[ISSN:1001-6015/CN:41-1162/R]

卷:
第36卷
期数:
2024年09期
页码:
49-58,75
栏目:
技术研究
出版日期:
2024-09-20

文章信息/Info

Title:
Molecular mechanisms of synovial lesions in steroid-induced osteonecrosis of the femoral head:an experimental study
作者:
方伟华1庄至坤2彭鹏1肖方骏1杨晓强1林锟1何伟3魏秋实3何敏聪3
(1.广州中医药大学第三临床医学院,广东 广州 510006; 2.泉州市正骨医院,福建 泉州 362000; 3.广州中医药大学第三附属医院,广东 广州 510378)
Author(s):
FANG Weihua1ZHUANG Zhikun2PENG Peng1XIAO Fangjun1YANG Xiaoqiang1LIN Kun1HE Wei3WEI Qiu-shi3HE Mincong3
1.The Third Clinical Medical College of Guangzhou University of Chinese Medicine,Guangzhou 510006,Guangdong,China 2.Quanzhou Orthopedic-Traumatological Hospital,Quanzhou 362000,Fujian,China 3.The Third Affiliated Hospital of Guangzhou University of Chinese Medicine,Guangzhou 510378,Guangdong,China
关键词:
股骨头坏死 糖皮质激素 滑膜炎 RNA测序 成纤维细胞 干扰素Ⅰ型
Keywords:
femur head necrosis glucocorticoids synovitis RNA-seq fibroblasts interferon typeⅠ
摘要:
目的:探讨激素性股骨头坏死(steroid-induced osteonecrosis of the femoral head,SONFH)滑膜病变的分子机制。方法:①转录组测序及生物信息学分析。收集9例接受全髋关节置换术的患者(SONFH患者3例、髋骨关节炎患者3例和股骨颈骨折患者3例)术中切除的髋关节滑膜组织,进行转录组测序和生物信息学分析,筛选SONFH滑膜病变核心基因。②滑膜组织检测。根据标本来源将髋关节滑膜组织分为SONFH组、髋骨关节炎组和股骨颈骨折组。观察各组髋关节滑膜组织的组织形态,采用实时定量PCR检测3组髋关节滑膜组织中SONFH滑膜病变核心基因的mRNA相对表达量,采用蛋白质印迹法和免疫组织化学染色法检测3组髋关节滑膜组织中SONFH滑膜病变核心基因的蛋白相对表达量。采用免疫荧光染色法检测SONFH滑膜病变的靶细胞。③细胞验证。培养大鼠滑膜成纤维细胞,构建滑膜炎细胞模型。采用实时定量PCR及蛋白质印迹法检测空白细胞(空白细胞组)和滑膜炎模型细胞(模型细胞组)中SONFH滑膜病变核心基因的表达。结果:①转录组测序和生物信息学分析结果。经对不同患者来源的髋关节滑膜组织进行差异基因分析,共筛选出1001个与SONFH髋关节滑膜病变相关的基因,这些基因与免疫反应和外泌体有关,其中干扰素调节因子(interferon regulatory factor,IRF)4和IRF7是SONFH髋关节滑膜病变的核心基因,两者均为参与Ⅰ型干扰素应答的关键转录因子。②滑膜组织形态观察结果。苏木素-伊红染色显示,股骨颈骨折组髋关节滑膜组织形态正常,无细胞增生、肥大或间质水肿; 髋骨关节炎组髋关节滑膜组织细胞增生,有少量新生血管和细胞聚集; SONFH组髋关节滑膜组织细胞大量增殖和聚集,有新生血管。③滑膜组织中SONFH滑膜病变核心基因表达检测结果。SONFH组髋关节滑膜组织中IRF4、IRF7、干扰素-α(interferon-α,IFN-α)的mRNA相对表达量均高于股骨颈骨折组和髋骨关节炎组(P=0.000,P=0.000,P=0.000; P=0.001,P=0.000,P=0.036),髋骨关节炎组髋关节滑膜组织中IRF4、IRF7、IFN-α的mRNA相对表达量均高于股骨颈骨折组(P=0.000,P=0.000,P=0.000)。IRF4、IRF7、IFN-α蛋白在SONFH组髋关节滑膜组织中高表达,SONFH组髋关节滑膜组织中IRF4、IRF7、IFN-α的蛋白相对表达量均高于股骨颈骨折组和髋骨关节炎组(P=0.001,P=0.000,P=0.000; P=0.000,P=0.014,P=0.000),髋骨关节炎组髋关节滑膜组织中IRF4、IRF7、IFN-α的蛋白相对表达量均高于股骨颈骨折组(P=0.002,P=0.005,P=0.000)。④SONFH滑膜病变靶细胞检测结果。SONFH组髋关节滑膜组织中IRF7、钙黏附蛋白11(cadherin-11,CDH-11)的蛋白相对表达量均高于股骨颈骨折组和髋骨关节炎组(P=0.001,P=0.000; P=0.000,P=0.001),髋骨关节炎组髋关节滑膜组织中IRF7、CDH-11的蛋白相对表达量高于股骨颈骨折组(P=0.001,P=0.000)。滑膜成纤维细胞为SONFH滑膜病变的靶细胞。⑤细胞验证结果。模型细胞组IRF4、IRF7、IFN-α的mRNA和蛋白相对表达量均高于空白细胞组(P=0.001,P=0.002,P=0.000; P=0.001,P=0.007,P=0.000)。结论:SONFH滑膜病变与免疫炎症反应关系密切,滑膜成纤维细胞可能是SONFH滑膜病变的靶细胞,IRF4和IRF7可能是其潜在的靶点。
Abstract:
Objective:To investigate the molecular mechanisms of synovial lesions in steroid-induced osteonecrosis of the femoral head(SONFH).Methods:①RNA sequencing(RNA-seq)and bioinformatics analysis.The hip synovial tissues were collected from patients with SONFH(3 ones),hip osteoarthritis(HOA)(3 ones)and femoral neck fracture(FNF)(3 ones),respectively,during the total hip arthroplasty for RNA-seq and bioinformatics analysis to screen the core genes of synovial lesions in SONFH.②Synovial tissues detection.The hip synovial tissue specimens were divided into SONFH group,HOA group,and FNF group based on their sources,and then were sectioned and stained with hematoxylin-eosin(HE)for observing the morphology.Furthermore,the relative mRNA expression levels of core genes of SONFH-triggered synovial lesions in the hip synovial tissues were detected by using real-time quantitative PCR(RT-qPCR),and the relative protein expression levels of core genes of SONFH-triggered synovial lesions in the hip synovial tissues were detected by employing Western blotting and immunohistochemical staining,respectively.Additionally,the target cells of SONFH-triggered synovial lesions were detected by immunofluorescence staining.③Cell validation.The rat synovial fibroblasts(SFs)were cultured to construct a synovitis-cell model,and the expression of core genes of SONFH-triggered synovial lesions in blank cells(blank cell group)and synovitis model cells(model cell group)were detected by using RT-qPCR and Western blotting,respectively.Results:①The results of RNA-seq and bioinformatics analysis.One thousand and one SONFH-triggered hip synovial lesions-associated genes were screened out by analysis on differentially expressed genes(DEGs)in hip synovial tissues from different patients,and they were all related to immune response and exosomes,with interferon regulatory factor(IRF)4 and IRF7 identified as the core genes for SONFH-triggered hip synovial lesions,both of which were the key transcription factors in participating in type I interferon responses.②The results of observation on morphology of synovial tissues.The result of HE staining showed that,in FNF group,the hip synovial tissues presented with a normal morphology,without cell proliferation,hypertrophy,or interstitial edema; the hip synovial tissues in HOA group exhibited cell proliferation,with a small amount of neovascularization and cell aggregation; while the marked changes,manifesting as a significant increase in cell proliferation and aggregation,with the neovascularization,were observed in hip synovial tissues of SONFH group.③The results of detection on the expression of core genes of SONFH-triggered synovial lesions in synovial tissues.The relative mRNA expression levels of IRF4,IRF7 and interferon-α(IFN-α)in hip synovial tissues were higher in SONFH group compared to FNF group and HOA group(P=0.000,P=0.000,P=0.000; P=0.001,P=0.000,P=0.036),and were higher in HOA group compared to FNF group(P=0.000,P=0.000,P=0.000).The IRF4,IRF7 and IFN-α proteins were highly expressed in the hip synovial tissues in SONFH group.The relative protein expression levels of IRF4,IRF7 and IFN-α in hip synovial tissues were higher in SONFH group compared to FNF group and HOA group(P=0.001,P=0.000,P=0.000; P=0.000,P=0.014,P=0.000),and were higher in HOA group compared to FNF group(P=0.002,P=0.005,P=0.000).④The results of detection on target cells of SONFH-triggered synovial lesions.The relative protein expression levels of IRF7 and cadherin-11(CDH-11)in hip synovial tissues were higher in SONFH group compared to FNF group and HOA group(P=0.001,P=0.000; P=0.000,P=0.001),and were higher in HOA group compared to FNF group(P=0.001,P=0.000).The SFs were identified as the target cells of SONFH-triggered synovial lesions.⑤The results of cell verification.The relative mRNA and protein expression levels of IRF4,IRF7,and IFN-α were higher in model cell group compared to blank cell group(P=0.001,P=0.002,P=0.000; P=0.001,P=0.007,P=0.000).Conclusion:The synovial lesions are closely related to immune-inflammatory responses in patients with SONFH.The SFs may be the target cells of SONFH-triggered synovial lesions,with IRF4 and IRF7 as its potential targets.

参考文献/References:

[1] JIN H,LI L,YU W,et al.The efficacy of acupuncture and moxibustion for early and middle-stage osteonecrosis of the femeral head:a systematic review and meta-analysis of randomized controlled trials[J].Medicine(Baltimore),2021,100(22):e26210.
[2] HOPKINS C,GENANT H K.Editorial for guidelines for clinical diagnosis and treatment of osteonecrosis of the femoral head in adults(2019 version)[J].J Orthop Translat,2020,21:A1.
[3] ATILLA B,BAKIRCIOGLU S,SHOPE A J,et al.Joint-preserving procedures for osteonecrosis of the femoral head[J].EFORT Open Rev,2020,4(12):647-658.
[4] HATANAKA H,MOTOMURA G,IKEMURA S,et al.Volume of hip synovitis detected on contrast-enhanced magnetic resonance imaging is associated with disease severity after collapse in osteonecrosis of the femoral head[J].Skeletal Radiol,2019,48(8):1193-1200.
[5] RABQUER B J,TAN G J,SHAHEEN P J,et al.Synovial inflammation in patients with osteonecrosis of the femoral head[J].Clin Transl Sci,2009,2(4):273-278.
[6] KORNICKA-GARBOWSKA K,GROBORZ S,LYNDA B,et al.Mitochondria transfer restores fibroblasts-like synoviocytes(FLS)plasticity in LPS-induced,in vitro synovitis model[J].Cell Commun Signal,2022,20(1):137.
[7] CRUZ-TOPETE D,CIDLOWSKI J A.One hormone,two actions:anti-andpro-inflammatory effects of glucocorticoids[J].Neuroimmunomodulation,2015,22(1/2):20-32.
[8] HMAMOUCHI I,PARUK F,TABRA S,et al.Prevalence of glucocorticoid-induced osteoporosis among rheumatology patients in Africa:a systematic review and meta-analysis[J].Arch Osteoporos,2023,18(1):59.
[9] PAVELKA K.Osteonecrosis[J].Baillieres best pract res clin rheumatol,2000,14(2):399-414.
[10] YOON B H,JONES L C,CHEN C H,et al.Etiologic classification criteria of arco on femoral head osteonecrosis part 1:glucocorticoid-associated osteonecrosis[J].J Arthroplasty,2019,34(1):163-168.
[11] MONT M A,ZYWIEL M G,MARKER D R,et al.The natural history of untreated asymptomatic osteonecrosis of the femoral head:a systematic literature review[J].J Bone Joint Surg Am,2010,92(12):2165-2170.
[12] PAP T,DANKBAR B,WEHMEYER C,et al.Synovial fibroblasts and articular tissue remodelling:role and mecha-nisms[J].Semin Cell Dev Biol,2020,101:140-145.
[13] DE LANGE-BROKAAR B J,IOAN-FACSINAY A,VAN OSCH G J,et al.Synovial inflammation,immune cells and their cytokines in osteoarthritis:a review[J].Osteoarthritis Cartilage,2012,20(12):1484-1499.
[14] PENG Y,ZHANG M,HU J.Non-coding RNAs involved in fibroblast-like synoviocyte functioning in arthritis rheumatoid:from pathogenesis to therapy[J].Cytokine,2024,173:156418.
[15] OKAZAKI S,NISHITANI Y,NAGOYA S,et al.Femoral head osteonecrosis can be caused by disruption of the systemic immune response via the Toll-like receptor 4 signalling pathway[J].Rheumatology(Oxford),2009,48(3):227-232.
[16] THOMPSON C D,MATTA B,BARNES B J.therapeutic targeting of IRFs:pathway-dependence or structure-based?[J].Front Immunol,2018,9:2622.
[17] DURBIN R K,KOTENKO S V,DURBIN J E.Interferon induction and function at the mucosal surface[J].Immunol Rev,2013,255(1):25-39.
[18] HE C,ZHENG S,LUO Y,et al.Exosome theranostics:biology and translational medicine[J].Theranostics,2018,8(1):237-255.
[19] NOONIN C,THONGBOONKERD V.Exosome-inflammasome crosstalk and their roles in inflammatory responses[J].Theranostics,2021,11(9):4436-4451.
[20] JEFFERIES C A.Regulating IRFs in IFN driven disease[J].Front Immunol,2019,10:325.
[21] TAMURA T,YANAI H,SAVITSKY D,et al.The IRF family transcription factors in immunity and oncogenesis[J].Annu Rev Immunol,2008,26:535-584.
[22] LOHOFF M,MAK T W.Roles of interferon-regulatory factors in T-helper-cell differentiation[J].Nat Rev Immunol,2005,5(2):125-135.
[23] CHUNG Y,CHANG S H,MARTINEZ G J,et al.Critical regulation of early Th17 cell differentiation by interleukin-1 signaling[J].Immunity,2009,30(4):576-587.
[24] SHARMA S,TENOEVER B R,GRANDVAUX N,et al.Triggering the interferon antiviral response through an IKK-related pathway[J].Science,2003,300(5622):1148-1151.
[25] HONDA K,YANAI H,NEGISHI H,et al.IRF-7 is the master regulator of type-I interferon-dependent immune responses[J].Nature,2005,434(7034):772-777.
[26] VAN BON L,COSSU M,RADSTAKE T R.An update on an immune system that goes awry in systemic sclerosis[J].Curr Opin Rheumatol,2011,23(6):505-510.
[27] SIMONS K H,DE VRIES M R,DE JONG R C M,et al.IRF3 and IRF7 mediate neovascularization via inflammatory cytokines[J].J Cell Mol Med,2019,23(6):3888-3896.
[28] TATEDA K,OKAZAKI S,NAGOYA S,et al.The suppression of TRIM21 and the accumulation of IFN-α play crucial roles in the pathogenesis of osteonecrosis of the femoral head[J].Lab Invest,2012,92(9):1318-1329.

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备注/Memo

备注/Memo:
基金项目:国家自然科学基金项目(82274544,82004392); 广东省基础与应用基础研究基金项目(2023A1515010551); 国家中医药管理局高水平中医药重点学科建设项目(zyyzdxk-2023106); 福建中医药大学中医骨伤科学学科开放课题资助项目(XGS2023008); 毕节市科学技术局2022年度“揭榜挂帅”项目(毕科合重大专项〔2022〕1号); 广东省中医骨伤研究院开放课题重点项目(GYH202101-01,GYH202101-04)
通讯作者:何敏聪 E-mail:min-cong.he@hotmail.com
更新日期/Last Update: 1900-01-01