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噬菌体/白细胞介素-4脂质体复合材料预防小鼠上颌扩弓后复发OA

Phage/interleukin-4 liposome composite prevents relapse after maxillary expansion in mice

中文摘要英文摘要

目的 探讨负载P11噬菌体和白细胞介素-4(IL-4)脂质体(LIP)的新型可注射水凝胶(GelMA/P11/IL4@LIP)预防小鼠上颌扩弓后复发的效果,为其临床应用提供实验依据.方法 本研究已获得医院实验动物伦理委员会批准.首先,构建上颌扩弓及复发模型,15只7周龄C57BL/6小鼠随机分为对照组、扩弓后3 d组、扩弓后7 d组、保持14 d组及复发7 d组,每组3只.各组小鼠分别于对应时间点,即0、3、7、21、28 d处死,取上颌骨及前颅部.通过micro-CT测量腭中缝区域骨参数和上颌切牙近中牙槽嵴顶间距(ICD);组织学染色观察成骨、破骨活动;免疫组织化学染色(IHC)分析巨噬细胞极化标志物(CD86、CD206)、间充质干细胞标志物[胶质瘤相关癌基因同源物1(Gli1)]及成骨相关标志物[Runt相关转录因子2(Runx2)、Osterix(OSX)]的表达量.随后,合成GelMA/P11/IL4@LIP复合材料,应用于小鼠扩弓及复发模型.24只7周龄C57BL/6小鼠随机分为空白对照组、GelMA组、GelMA/P11组及GelMA/P11/IL4@LIP组,每组6只.所有小鼠均进行扩弓.扩弓后7 d,使用树脂固定所有小鼠的扩弓装置,进行14 d的保持.在保持期的第1天,分别向各组小鼠腭中缝区域注射生理盐水、GelMA溶液、GelMA/P11溶液及GelMA/P11/IL4@LIP溶液.14 d的保持期后,每组中随机选择3只小鼠处死;另外3只小鼠去除扩弓装置,经过7 d的复发后处死,取上颌骨及前颅部.通过micro-CT、组织学染色及免疫组化染色,探究GelMA/P11/IL4@LIP复合材料对扩弓后复发的预防作用.结果 小鼠上颌扩弓及复发模型中,micro-CT测量结果显示,复发7 d组ICD较保持14 d组下降(P=0.008);IHC分析显示,腭中缝区域M1型巨噬细胞持续浸润,Gli1+间充质干细胞数量少,成骨相关标志物(RUNX2、OSX)表达下降(P<0.001).GelMA/P11/IL4@LIP复合材料腭中缝局部注射后,与空白对照组、GelMA组相比,复发期ICD增大,巨噬细胞M2极化及Gli1+间充质干细胞募集增强,RUNX2和OSX表达量上调(P<0.05).结论 上颌扩弓后复发的机制为腭中缝M1巨噬细胞持续浸润、间充质干细胞募集及成骨分化不足.GelMA/P11/IL4@LIP复合材料可促进口颌面部间充质干细胞募集和成骨分化,并促进巨噬细胞适时向M2极化,增强腭中缝成骨,有效预防上颌扩弓复发.

Objective To explore the efficacy of a novel injectable hydrogel(GelMA/P11/IL4@LIP)loaded with P11 bacteriophages and interleukin-4(IL-4)liposomes(LIP)in preventing relapse after maxillary expansion in mice,providing experimental evidence for its clinical application.Methods This study was approved by the experimental animal ethics committee of our hospital.First,15 7-week-old C57BL/6 mice were used to establish a maxillary expan-sion model and divided into 5 groups(3 mice in each group):a control group,post expansion day 3 group(PED3 group),post expansion day 7 group(PED7 group),retention for 14 days group(RET group),and relapse for 7 days group(REL group).The mice in each group were sacrificed at their designated time points(day 0,3,7,21,28),and their maxilla and anterior cranial regions were collected.Bone parameters and the inter-crestal distance(ICD)of maxillary incisor mesial alveolar ridge were measured using micro-computed tomography(micro-CT).Histological staining was performed to evaluate bone formation and resorption,while immunohistochemistry(IHC)was performed for macrophage markers(CD86 and CD206),mesenchymal stem cell markers(glioma-associated oncogene homolog 1[Gli1]),and osteogenic markers(Runt-related transcription factor 2[Runx2]and Osterix[OSX]).Next,GelMA/P11/IL4@LIP was synthesized and administered to mouse models of maxillary expansion.A total of 24 7-week-old C57BL/6 mice were divided into 4 groups(6 mice in each group):a blank control group,GelMA group,GelMA/P11 group,and GelMA/P11/IL4@LIP group.All mice underwent palatal expansion.On PED7,the expanders of all 24 mice were cemented with resin to initi-ate the 14-day retention period.On day 1 of the retention phase,the mice in each group received injections of saline,GelMA,GelMA/P11,or GelMA/P11/IL4@LIP at the midpalatal suture.After the 14-day retention period,three mice in each group were randomly selected and sacrificed,while the other three had their expanders removed and underwent a 7-day relapse before being sacrificed on day 28(REL).Micro-CT,histological staining,and IHC were performed to evaluate the preventive effect of GelMA/P11/IL4@LIP on post-expansion relapse.Results The mice maxillary expan-sion model exhibited a decreased ICD at REL compared to RET in micro-CT analysis(P=0.008).IHC analysis demon-strated prolonged M1 macrophage infiltration,scarce Gli1+mesenchymal stem cells,and insufficient expression of osteo-genic markers(RUNX2 and OSX)(P<0.001).Compared to the blank control and GelMA groups,GelMA/P11/IL4@LIP hydrogel injection in the midpalatal suture led to increased ICD at REL,promoted the timely M2 polarization of macro-phages,recruited Gli1+mesenchymal stem cells,and upregulated the expression of RUNX2 and OSX(P<0.05).Con-clusion The mechanism of relapse after maxillary expansion involves the persistent infiltration of M1 macrophages,as well as the inadequate recruitment and insufficient osteogenic differentiation of MSCs in the midpalatal suture.The GelMA/P11/IL4@LIP composite enhanced orofacial mesenchymal stem cell recruitment and promoted the M2 polariza-tion of macrophages,thereby enhancing osteogenesis in the midpalatal suture and preventing post-expansion relapse.

李睿智;刘偌景;汪兴明;蒲曦鸣;尹星;邹淑娟

口腔疾病防治全国重点实验室 国家口腔医学中心 口腔疾病国家临床医学研究中心 四川大学华西口腔医院正畸科,四川 成都(610041)四川省人民医院温江医院 成都市温江区人民医院正畸科,四川 成都(611130)四川大学生物医学工程学院,四川 成都(610065)四川大学生物医学工程学院,四川 成都(610065)口腔疾病防治全国重点实验室 国家口腔医学中心 口腔疾病国家临床医学研究中心 四川大学华西口腔医院正畸科,四川 成都(610041)口腔疾病防治全国重点实验室 国家口腔医学中心 口腔疾病国家临床医学研究中心 四川大学华西口腔医院正畸科,四川 成都(610041)

医药卫生

间充质干细胞巨噬细胞噬菌体噬菌体展示技术白细胞介素-4上颌扩弓上颌横向发育不足免疫调节

mesenchymal stem cellsmacrophagesphagephage display techniquesinterleukin-4maxil-lary expansionmaxillary transverse deficiencyimmunomodulation

《口腔疾病防治》 2026 (6)

529-540,12

国家自然科学基金面上项目(82271017)四川省科技计划项目重点研发项目(2022YFS0117)爱齐科研专项基金项目(AQKY22-1-2AQKY22-2-6) This study was supported by the grants from National Natural Science Foundation of China(No.82271017)Sichuan Provincial Department of Science and Technology Applied Basic Research(No.2022YFS0117)Align Technology Re-search Program(No.AQKY22-1-2 and No.AQKY22-2-6).

10.12016/j.issn.2096-1456.202550506

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