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Here we show that VacA permeabilizes the apical membrane of gastric parietal cells and induces hypochlorhydria.The functional consequences of VacA infection on parietal cell physiology were studied using freshly isolated rabbit gastric glands and cultured parietal cells.Secretory activity of parietal cells was judged by aminopyrine uptake assay and confocal microscopic examination.

为此,我们建立了原代培养的胃腺、胃壁细胞等研究模型和良好的评估壁细胞分泌能力的技术平台,包括氨基比林吸收实验、激光共聚焦扫描技术等,对VacA感染所导致的壁细胞生理特征的改变进行了深入细致的研究。

Results True positive rate: immature granulocyte, hemoglobin concentration variation, microcyte, left shift, macrocyte, hypochromic erythrocyte, large platelet, blasts, anisocytosis 86.7%-100.0%, hyperchromic erythrocyte 69.2%, nucleated red blood cell, atypical lymphocyte, platelet clumps

结果 真阳性率:未成熟粒细胞、血红蛋白浓度不等、小红细胞、核左移、大红细胞、低色素性红细胞、大血小板、原幼细胞、红细胞大小不等为86.7%~100.0%,高色素性红细胞为69.2%,有核红细胞、变异淋巴细胞、血小板凝集为13.3%~32.3%;以上所有参数真阴性率为82.8%~100.0%(平均95.0%)。

Objective: Augmenter of liver regeneration cloned from liver of weaning rat is a novel hepatic stimulator. It was reported that ALR mRNA expression was correlated with DNA synthesis of hepatocytes after partial hepatectomy, and could significantly promote the survial rate of intoxicated hepatitis rats.

目的:肝再生增强因子是从新生大鼠肝组织中克隆到的一种肝增殖刺激因子,其特异mRNA的表达与大鼠肝部分切除后肝细胞DNA合成密切相关,是一种特殊的促肝细胞分裂原,能特异地刺激肝细胞增殖,是肝再生的重要调控因子,能提高中毒性肝损伤动物的存活率,在肝损伤修复过程中发挥作用。

The biological analysis results showed: Population Doubling Time of cells was approximately 24 h;Diploid account for 76%~88% in cell's chromosome;By Isozyme analysis of Lactic Dehydrogenase,Malic Dehydrogenase,cross contamination had not taken place;The test results of ...

结果表明:细胞群体倍增时间约为24 h;细胞染色体中二倍体(2n=60)占主体,镜检细胞的百分比为98.2%;乳酸脱氢酶、苹果酸脱氢酶同工酶分析,没有其他物种污染;细菌、真菌、病毒、支原体检测阴性。

The main production as following:1. The effect of cerium on primary hepatocyte was studied by flow cytometry.

主要成果如下:1 应用流式细胞术研究了稀土离子对大白鼠原代肝细胞和肝癌细胞的影响。

The calcified nodules were found at days 20 of primary culture in osteoblasts, with more cellular fission in growing period. Cell process was mutual linkage and arranged in shape of typical "cobble-stone" when reached a confluence.

成骨细胞原代培养20 d时出现不透光的钙化结节,生长期细胞分裂相多见,细胞突起相互连接,汇合时呈铺路石状。

In addition, using RT-PCR to detect expression of centrin homogene during Urechis unicinctus spermatid deferentiation and early embryonic development. The result revealed that (1) expression of HsCEN1 homogene is present during spermatid defferentiation including spermtid and sperm, but not in adult tissues including body wall tissue,intestinal mucous memberane cells and cell in coelom succus;(2) expression of HsCEN1 homogene is not present in unfertilized oocytes but present in that of released polar bodies after fertilization and parthenogenesis oocytes treated with A23187;(3) expression of HsCEN1 homogene is present during early embryonic development including two-cell stage,multicell stage,gastrula to trochophora.

我们还用RT-PCR方法检测了Centrin同源基因在单环刺螠精子分化过程和早期胚胎发育过程的表达,结果显示:在单环刺螠精子发生过程中的精细胞、精子团、精子中都有表达,而在成体的体壁组织、消化道组织、体腔球中则没有表达;在未受精卵中没有表达,而在受精后释放极体的受精卵和经A23187孤雌激活的卵中则有表达;在单环刺螠的早期发育过程——二细胞胚胎、多细胞胚胎、原肠胚、早期担轮幼虫——中都有表达。

Six days after inoculation, the cucumber root tip was slightly swollen and symmetrical root-knots were observed at the meristematic and elongation zones. Giant cells were differentiated by previous cambium cells in the center of the root; 10days after inoculation, symmetrical and secondary root-knots were observed at the root hair and upper zones. Vessels were separated by giant cells, around which protoxylem vessels were observed; l6days after inoculation, hypo-vascular tissue appeared earlier than normal; 20-30 days after inoculation, the vertical arrangement of vessels was disordered, shape was distorted and a new vascular tissue appeared in the cortex.

结果显示:接种后6 d的根尖分生区、伸长区出现膨大、对称的根结,根中心的原形成层细胞分化出巨型细胞;10 d在根毛区及以上部位出现既有对称又有偏于一侧的根结,周围有原生木质部导管出现,根结中巨型细胞阻断了导管;16 d次生维管组织提早出现;20~30 d导管纵向排列无序,形状扭曲,皮层中有新维管组织产生。

MTT assay was used to measure the cell survival after laser irradiation. Results 5-ALA cocultured with U251 cells successfully produced endogenous Pp Ⅸthat was observed distributively in the cytoplasm, but not in nuclear region.

将5-ALA加入U251细胞中,随之以635 nm的激光辐射,使用MTT法测定细胞生存率结果5-ALA与U251细胞共培养可以产生光敏剂原卟啉。

OMFs were observed under electroscope and investigated in histology after

结果 成功建立大鼠OMF种子细胞库,原代细胞与传代细胞在形态和生长速度上无显著差异。

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