锌指蛋白440在人膝关节OA软骨细胞损伤中的促进作用及机制

探讨锌指蛋白440（ZNF440）在膝关节（Knee）骨性关节炎（OA）软骨细胞损伤和退化变性病理生理学中的作用。方法 Knee软骨中分离人软骨细胞,分为对照组、Knee OA组、ZNF440-GFP（绿色荧光蛋白）组、ZNF440-siRNA组和Scriptaid组。通过免疫组化和Western blotting测定ZNF440在Knee OA软骨中的表达。用ZNF440-GFP过表达和ZNF440-siRNA转染细胞,并给予白细胞介素-1β(IL-1β)刺激。分别用qPCR和WB检测分解代谢、合成代谢和凋亡相关标志物的mRNA和蛋白表达水平。生物信息学分析有可能抑制ZNF440表达的化合物。结果 与对照组相比,ZNF440在Knee OA软骨中的表达有所增加(P＜0.05);ZNF440过表达明显增加基质金属蛋白酶（MMP）13和PARP p85的表达,并降低COL2A1表达(P＜0.05);siRNA敲除ZNF440可部分逆转IL-1β刺激诱导的人Knee OA软骨细胞的分解代谢和细胞凋亡(P＜0.05)。通过生物信息学分析和验证实验,确定Scriptaid是一种有可能下调ZNF440表达的化合物。Scriptaid处理可降低OA软骨细胞中ZNF440的表达,同时降低过表达ZNF440的人Knee OA软骨细胞中MMP13和PARP p85的表达(P＜0.05)。结论 ZNF440在人Knee OA软骨中的表达明显增加,可能通过调节细胞中炎症、分解代谢和凋亡标志物的表达参与软骨退行性机制。此外,Scriptaid可降低ZNF440的表达,并抑制其在OA软骨细胞中的破坏作用     

膝关节盘状半月板损伤患者关节镜术后疼痛的列线图预测模型构建

目的 分析膝关节盘状半月板(DLM)损伤患者关节镜术后疼痛的危险因素,并构建列线图预测模型。方法 收集2017年1月至2021年12月行关节镜手术治疗的217例DLM损伤患者临床资料。依照NRS数字分级法评估术侧膝关节及髌周疼痛情况,将患者分为疼痛组(≤4分,n=26)和非疼痛组(≥4分,n=191)。采用受试者工作特征(ROC)曲线分析获取有统计学意义的连续性变量的最佳截断值。采用多因素logistic回归模型分析DLM损伤患者关节镜术后疼痛的危险因素。构建预测DLM损伤患者关节镜术后疼痛的列线图预测模型,采用校正曲线对列线图预测模型进行内部验证和性能评价,决策曲线对列线图预测模型的预测效能进行临床净收益评估。结果 疼痛组患者年龄、关节软骨损伤比例、术后无冷敷比例均高于非疼痛组(P<0.05),术后负重时间早于非疼痛组(P<0.05)。ROC曲线分析显示：年龄、术后负重时间的AUC分别为0.767、0.774;最佳截断值分别为54岁、7 d。年龄(>54岁)、关节软骨损伤(有)、术后负重时间(≤7 d)是DLM损伤患者关节镜术后疼痛的独立危险因素,术后冷敷(有)是D...     

格隆溴铵对高氧诱导幼鼠急性肺损伤的影响及其机制研究

目的 探究格隆溴铵对高氧诱导幼鼠急性肺损伤（ALI）的影响及作用机制。方法 从30只SD幼鼠中随机选取10只为对照组,其余幼鼠成功复制高氧诱导的ALI模型,随机分为ALI组、格隆溴铵组,每组10只。格隆溴铵组雾化吸入0.8 mg/（kg·d）格隆溴铵,ALI组、对照组吸入等体积生理盐水,连续给药7 d后,测量幼鼠肺组织湿/干重比值（W/D）、肺指数,检测白细胞介素-1β（IL-1β）、白细胞介素-6（IL-6）及肿瘤坏死因子-α（TNF-α）水平及血清活性氧基团（ROS）、超氧化物歧化酶（SOD）水平,比较肺组织病理学变化及Toll样受体4/髓分化因子88（TLR4/MyD88）通路蛋白的表达。结果 与对照组比较,ALI组W/D及肺指数升高（P <0.05）,血清IL-1β、IL-6、TNF-α、SOD水平升高（P <0.05）,ROS水平降低（P <0.05）,TLR4、MyD88蛋白相对表达量上调（P <0.05）;与ALI组比较,格隆溴铵组W/D及肺指数降低（P <0.05）,血清IL-1β、IL-6、TNF-α、SOD水平降低（P <0.05）,ROS水平升高（P <0.05）,TLR4、MyD88蛋白相对表达量下调（P <0.05）。结论 格隆溴铵能改善血清炎症指标及氧化应激指标,降低高氧诱导的ALI,其作用机制可能与TLR4/MyD88通路有关。     

Th17/Treg细胞免疫平衡的相关调控机制研究进展

免疫系统可识别、抵抗病原微生物及清除体内异常分裂的细胞,平衡的免疫系统对维持正常的机体反应活动至关重要。人体内的多种细胞都可参与维持免疫稳态,其中辅助性T淋巴细胞17（Th17）和调节性T淋巴细胞（Treg）发挥着重要作用,失衡的免疫系统可致多种免疫性疾病的发生。Th17/Treg细胞平衡受细胞因子、代谢、肠道微生态及翻译后修饰等多种机制调控,该文通过总结相关机制为免疫性疾病治疗提供新思路和策略。     

基于太赫兹时域光谱技术的名贵动物药材龟甲的真伪品鉴别

目的： 建立一种利用太赫兹时域光谱和多种化学计量学方法鉴别龟甲真伪的新方法。方法： 选用正品乌龟和伪品红耳彩龟的腹甲进行实验,先用经典的性状鉴别、显微鉴别方法比较两种样品的典型性状特征,后利用太赫兹时域光谱仪测得样品的光谱信息,对样品谱图进行平滑处理和基线校准,并运用化学计量方法进行数据分析以区分正品和伪品龟甲。结果： 性状鉴别结果显示完整正、伪品龟甲样品仅有细微差异,且其碎片或粉末基本无差异;显微鉴别未在两种样品中发现明显的特征差异性结构;两种样品的太赫兹时域光谱曲线图经快速傅里叶变换滤波器平滑滤波处理、正交偏最小二乘法判别分析处理后呈现显著差异。结论： 利用太赫兹时域光谱技术结合正交偏最小二乘法判别分析可以实现龟甲真伪品的精准鉴别。     

肝脏子宫内膜异位症一例

肝脏子宫内膜异位症是以肝内存在异位子宫内膜为特征的一种罕见子宫内膜异位症类型,因其缺乏典型临床症状且影像学诊断困难,易被误诊,组织学检查目前仍是肝脏子宫内膜异位症诊断的金标准。现报告1例海军军医大学第三附属医院收治的患者,反复经期右上腹疼痛,经超声检查发现右肝占位性病变,术后病理证实为肝脏子宫内膜异位症。     

屈光度对SMILE术后眼压的预测和校正

目的 探究SMILE术后眼压的预测并校正。方法 回顾性研究+前瞻性验证。纳入2019-12/2021-12于中部战区总医院行SMILE的患者90例(180眼),随机抽取30眼为验证集,余150眼为训练集。前瞻性录入2022-01/2022-09SMILE的51例(102眼)为测试集。首先分析训练集手术前3d、术后1wk、1mo、3mo及6mo的眼压情况,确定眼压稳定期及于术前的眼压变化量(ΔIOP);再选取球柱镜代数和(SC)、球镜度(DS)、柱镜度(DC)及眼压(IOP)、中央角膜厚度(CCT)、角膜平均曲率(Km)、前房深度(ACD),眼压稳定时的变化量(ΔCCT、ΔKm、ΔK1、ΔK2、ΔACD)及个体因素,纳入与ΔIOP相关的因素拟合回归模型;最后建立适合临床SMILE术后眼压预测及校正的公式并作效能验证。结果 除术后1wk、3mo及6moIOP三者间无明显差异外,余时段IOP间差异均有统计学意义(P＜0.05);各因素与ΔIOP拟合最佳回归方程：ΔIOP=0.459IOP_术前-0.183SC-0.041Age+1.292ΔACD-1.270(调节R₂^=0.533,P＜0.001)。仅纳入术前IOP和SC,拟合简化方程：ΔIOP=0.496IOP_术前-0.194SC-2.952(调节R₂^=0.498,P＜0.001);预测和校正公式：IOP_术后预测=0.5IOP_术前+0.2SC+3,IOP_术后校正=IOP_术后+0.5IOP_术前–0.2SC–3。简化公式的效能验证显示良好。结论 SMILE术后3月IOP趋于稳定,且ΔIOP与屈光度相关。SMILE术后IOP可通过简化公式作快速临床预测和校正。     

AO肩锁钢板钩治疗重型肩锁关节脱位

目的评估AO肩锁钢板钩治疗重型肩锁关节脱位的手术疗效.方法回顾性分析两年来27例手术病人的手术治疗和疗效.结果手术方法符合生理结构,手术时间平均30分钟,内固定牢靠.根据Murley和Constant[1]评分,优良率94%.结论 AO肩锁钢板钩治疗重型肩锁关节脱位,手术方法简单,疗效可靠,允许病人术后早期功能锻炼.     

Attachment and spreading of fibroblasts on an RGD peptide-modified injectable hyaluronan hydrogel

Hyaluronan (HA) hydrogels resist attachment and spreading of fibroblasts and most other mammalian cell types. A thiol-modified HA (3,3'-dithiobis(propanoic dihydrazide) [HA-DTPH]) was modified with peptides containing the Arg-Gly-Asp (RGD) sequence and then crosslinked with polyethylene glycol (PEG) diacrylate (PEGDA) to create a biomaterial that supported cell attachment, spreading, and proliferation. The hydrogels were evaluated in vitro and in vivo in three assay systems. First, the behavior of human and murine fibroblasts on the surface of the hydrogels was evaluated. The concentration and structure of the RGD peptides and the length of the PEG spacer influenced cell attachment and spreading. Second, murine fibroblasts were seeded into HA-DTPH solutions and encapsulated via in situ crosslinking with or without bound RGD peptides. Cells remained viable and proliferated within the hydrogel for 15 days in vitro. Although the RGD peptides significantly enhanced cell proliferation on the hydrogel surface, the cell proliferation inside the hydrogel in vitro was increased only modestly. Third, HA-DTPH/PEGDA/peptide hydrogels were evaluated as injectable tissue engineering materials in vivo. A suspension of murine fibroblasts in HA-DTPH was crosslinked using PEGDA plus PEGDA peptide, and the viscous, gelling mixture was injected subcutaneously into the flanks of nude mice; gels formed in vivo following injection. After 4 weeks, growth of new fibrous tissue had been accelerated by the sense RGD peptides. Thus, attachment, spreading, and proliferation of cells is dramatically enhanced on RGD-modified surfaces but only modestly accelerated in vivo tissue formation.     

Collagen-coated polylactide microspheres as chondrocyte microcarriers

Polylactide (PLA) microspheres were coated with collagen for cell culture and injectable cell carriers. Utilizing a method of emulsion-solvent evaporation, PLA microspheres with diameter ranging from 180 to 280 microm were prepared, followed with aminolysis in hexanediamine/n-propanol solution to introduce free amino groups on their surfaces. After the amino groups were transferred into aldehyde groups by a treatment of glutaraldehyde, collagen type I was covalently coupled via Schiff base formation between the aldehyde groups and the amino groups on collagen molecules. Meanwhile, physically entangled collagen molecules were retained following a grafting-coating protocol to yield microspheres coated with larger amount of collagen. Aminolysis resulted in weight loss of the microspheres following a linear relationship with the aminolysis time. The NH2 and collagen contents existed on the microsphere surface were quantitatively determined by ninhydrin and hydroproline (Hyp) analyses, respectively. Larger amount of collagen was immobilized on the microspheres with higher content of NH2. In vitro chondrocyte culture revealed that the cells could attach, proliferate and spread on these PLA microspheres, in particular on the ones having higher content of collagen. These results show that the collagen-coated PLA microspheres are promising candidate as cell microcarriers.