"双固一通"艾灸法对糖尿病及糖尿病周围神经病变大鼠海马BDNF和NT-3蛋白的影响

目的观察“双固一通”艾灸法对糖尿病DM 及糖尿病周围神经病变(DPN)大鼠血糖及海马中神经营养因子(BDNF)和神经营养素-3(NT-3)蛋白的影响。方法75只雄性SD大鼠随机分为A组、B组、C组、D组和E组,每组15只。A组为正常对照组,不进行任何干预,B组为DM模型组,造模后不行艾灸干预;C组为DM艾灸治疗组,采用艾条悬灸;D组为DPN模型组,造模后不行艾灸干预;E组为DPN艾灸治疗组,采用艾条悬灸。于造模后72 h、4周治疗结束后和8周治疗结束后空腹尾静脉采血测血糖,于4周治疗结束后和8周治疗结束后,用免疫组化试验方法检测各组大鼠海马中BDNF和NT-3蛋白表达情况。结果B组、D组与A组血糖水平比较,差异有统计学意义(P<0.05),C组与B组比较,大鼠血糖水平降低(P<0.05);E组与D组比较,大鼠血糖水平降低(P<0.05)。B组、D组大鼠海马BDNF及NT-3免疫阳性神经元平均光密度值较A组明显减少(P<0.05);与B组比较,C组大鼠BDNF及NT-3免疫阳性神经元平均光密度值明显增加(P<0.05);与D组比较,E组大鼠BDNF及NT-3免疫阳性神经元平均光密度值明显增加(P<0.05)。结论“双固一通”艾灸法不仅可以起到明显的降糖效果,还可通过影响BDNF和NT-3蛋白的产生,保护糖尿病大鼠的感觉神经元,并对糖尿病及并发症周围神经病变起到治疗作用。     

PVT1 induces NSCLC cell migration and invasion by regulating IL-6 via sponging miR-760

Non-small-cell lung carcinoma (NSCLC) accounts for approximately 80% of lung cancers with a high metastatic potential. Elucidating the mechanism of NSCLC metastasis will provide new promising targets for NSCLC therapy and benefit its prognosis. Plasmacytoma variant translocation 1 (PVT1) has been proven to be overexpressed in NSCLC. Although the oncogenic role of PVT1 in NSCLC has been reported, its mechanism remains unclear. Here, we verified that the knockdown of PVT1 inhibited NSCLC cell migration and invasion, and that its inhibitory role on A549 cells and H1299 cells was antagonized by interleukin-6 (IL-6) treatment. The results revealed that PVT1 regulates IL-6 by sponging miR-760 and identified the binding site of miR-760 in the 3′-UTR of IL-6. In conclusion, a new mechanism was revealed, wherein PVT1 regulates NSCLC cell migration and invasion via miR-760/IL-6, suggesting PVT1/miR-760/IL-6 as promising prognostic biomarkers and therapeutic targets for NSCLC metastasis.     

Cytoskeleton of cells in vocal fold macula flava unphonated for a long period

Cells in the maculae flavae (MFe) are inferred to be involved in the metabolism of extracellular matrices of the human vocal fold mucosa. The latest research has supported the hypothesis that the tension caused by phonation (vocal fold vibration) regulates the behavior of these cells in the MFe of the human vocal fold. Tensile and compressive strains have direct effects on cell morphology and structure including changes in cytoskeletal structure and organization. Cytoskeletons are one of the structures which play a role as mechanoreceptors for the cells. The microstructure of the intermediate filaments and the expression of their proteins were investigated regarding the cells in the MFe of the human vocal fold unphonated over a decade. The adult vocal fold mucosa of a 64-year-old male with cerebral hemorrhage unphonated for 11 years was investigated by immunohistochemistry and electron microscopy. The intermediate filaments in the cytoplasm of the cells had become fewer in number. And the expression of their characteristic proteins (vimentin, desmin, GFAP) was also reduced. The results of this study are consistent with the hypothesis that mechanotransduction caused by vocal fold vibration could possibly be a factor in regulating the function and fate of the cells in the MFe.     

Clinicopathologic significance of LAIR-1 expression in hepatocellular carcinoma

Aim

Leukocyte-associated immunoglobulin-like receptor-1 (LAIR-1) is an immune inhibitory receptor which is expressed within most types of hematopoietic cells and negatively regulates immune responses. Recently, we found LAIR-1 expression to be present within tumors of nonhematopoietic lineages. However, the roles of LAIR-1 in hepatocellular carcinoma (HCC) have yet to be examined. The purpose of this study was to investigate the expression of LAIR-1 in HCC tissue and assess its clinical significance at this site.

Beclin 1 基因对恶性胶质瘤细胞 U87 自噬活性和增殖的影响简

目的研究BeclinJ基因对U87胶质瘤细胞自噬和增殖的影响。方法实验分5组：空白对照组．pSUPER—Bec组（表达BeclinsiRNA）与其阴性对照组（pSUPER—non组）,pcDNA3．1-Bec组（表达BeclinJ基因质粒）与其阴性对照组（pcDNA3．1-non组）。分别转染U87细胞,采用免疫印迹检测Beclin1、LC3和p62蛋白在各组的表达;用氚标胸腺嘧啶脱氧核苷（3H-TdR）检测各组细胞增殖率。结果转染后48h,pSUPER—Bec组Beclin1、LC3B—11蛋白表达下降,p62蛋白表达升高。pcDNA3．1-Bec组Beclin1、LC3B-Ⅱ蛋白表达升高,p62蛋白表达下降。与空白对照组或pcDNA3．1-non组相比．pcDNA3．1-Bec组细胞增殖速度降低（P〈0．05）,其他各组细胞增殖速度无明显差异。结论恶性胶质瘤细胞中自噬相关基因Beclinj表达下降,过表达Beclinl蛋白能增强细胞的自噬活性,抑制细胞的增殖活性。     

血清YKL-40水平与胶质瘤病理分级及预后的相关性研究

目的探讨血清YKL-40水平与胶质瘤病理分级及预后的相关性。方法选取诊断为脑胶质细胞瘤并行手术治疗的成年病例68例为胶质瘤组,20例健康体检病人作为对照组,根据术后病理学分级,低度恶性Ⅰ级2例、Ⅱ级17例,高度恶性Ⅲ级15例、Ⅳ级34例。观察生存时间及复发时间,生存时间〈12个月15例,12～24个月15例,〉24个月38例。复发前死亡10例,复发时间〈12个月14例,12～24个月15例,〉24个月未复发29例。术前均抽取静脉血采用酶联免疫吸附试验（ELISA）测定血清YKL-40水平。结果低级别（I级、Ⅱ级）胶质瘤病人血清YKL-40水平与对照组无显著差异（P〉0.05）,Ⅳ级胶质瘤病人血清YKL-40水平显著高于其他组（P〈0.05）。生存时间〈12个月和12～24个月的病人血清YKL-40水平显著高于生存时间〉24个月的病人（P〈0.05）。复发病人血清YKL-40水平显著高于未复发者（P〈0.05）,12个月内复发的病人血清YKL-40水平显著高于12～24个月复发的病人（P〈0.05）。结论血清YKL-40水平与胶质瘤的病理学分级及预后密切相关,可作为恶性程度及预后的判断指标。     

全腹腔镜及腹腔镜辅助远端胃癌毕Ⅰ式胃肠道重建的对比研究

目的:探讨全腹腔镜毕Ⅰ式胃肠道重建(三角吻合)的可行性、安全性及临床疗效。方法:回顾分析2013年6月至2014年1月施行的41例腹腔镜远端胃癌根治术的临床资料,其中23例行全腹腔镜毕Ⅰ式胃肠道重建术(三角吻合,A组),18例行腹腔镜辅助毕Ⅰ式胃肠道重建术(B组),对比分析两组患者的手术疗效。结果:两组患者胃肠道重建时间[(24±12)min vs.(26±15)min]、术后首次进流食时间[(3.7±1.8)d vs.(3.9±2.1)d]、术后住院时间[(8.5±2.7)d vs.(8.7±2.9)d]差异无统计学意义。A组止痛药使用次数明显少于B组[(1.7±1.5)vs.(3.5±1.9),P<0.05]。术后随访3~10个月,均未发生吻合口狭窄、吻合口漏、吻合口出血等手术并发症。结论:全腹腔镜毕Ⅰ式胃肠道重建(三角吻合)是安全、可行的,近期疗效满意,远期疗效尚需进一步观察研究。     

人骨唾液蛋白非融合荧光蛋白载体的构建及在乳腺癌细胞中的表达

背景：人骨唾液蛋白基因在矿化组织以外的易发生骨转移的人乳腺癌中表达。临床观察显示骨转移处的乳腺癌细胞骨唾液蛋白的表达量要高于原发部位的乳腺癌细胞，因此骨唾液蛋白有可能与肿瘤特异性骨转移的关系密切。研究乳腺癌骨转移可为将来临床的预防和治疗提供新的药物靶点。目的：建立骨唾液蛋白的稳定表达乳腺癌细胞系，观察骨唾液蛋白在乳腺癌骨转移的整个过程中的作用。设计：对照实验。单位：华南理工大学生物科学与工程学院，解放军广州军区广州总医院医学实验中心。材料：实验于2003-11／2004-03在解放军广州军区广州总医院医学实验室完成。质粒、菌种和细胞：pIRES2-EGFP载体质粒，E．Coli．Top10、含有人骨唾液蛋白基因全长的克隆载体pB-hBSP和发生特异性骨转移以及脑转移的人乳腺癌细胞株MDA-MB-231BO和MDA-MB-23lBR。方法：将人骨唾液蛋白基因通过聚合酶链式反应的方法从构建好的pB-hBSP载体中亚克隆出来，在其5’和3’端分别引入BglⅡ和PsiⅠ限制性酶切位点，定向克隆至真核表达载体pIRES2-EGFP，构建重组载体pIRES2-hBSP-EGFP。利用脂质体转染的方法将构建好的重组质粒转入特异性脑转移和骨转移的乳腺癌细胞株MDA-MB-231BR和MDA-MB-231BO中。主要观察指标：pIRES2-hBSP-EGFP重组表达载体的构建。重组表达载体pIRES2-hBSP-EGFP转染乳腺癌细胞。结果：①成功构建人骨唾液蛋白和绿色荧光蛋白非融合表达的真核表达载体pIRES2-hBSP-EGFP。②成功转染特异骨转移和脑转移的乳腺癌细胞株，可在荧光显微镜下观察到荧光蛋白标记，人骨唾液蛋白得到相应表达。结论：真核表达载体pIRES2-hBSP-EGFP的构建及转染可为骨唾液蛋白在乳腺癌骨转移中的作用的体内、外研究奠定一定的基础。