细胞板

蚕豆（Viciafaba）有丝分裂和减数分裂过程中细胞板形成的细胞化学研究

Cytochemical studies on cell plate formation during mitosis and meiosis of Vicia faba

结果表明：农药代森铵具有明显的诱变作用和毒性特征，其作用方式主要表现为对细胞板的抑制和染色体DNA的断裂作用。

The results show that Ambam has the effect of inducing obviously aberration and toxic properties . The way of its effect mainly expresses in the inhibition to cell plate and the breakage of DNA in chromosome .

MTT比色法结果与血细胞板计数法结果一致。

The result of MTT was consistent to that of cell count technique .

方法应用莱姆德细胞板通过补体依赖微量细胞毒性试验检测受者的群体反应性抗体（PRA）；

Methods Recipient 's panel reactive antibody ( PRA ) was detected by using micro complement dependent lymphocytotoxicity test with Lambda cell tray .

结果经NAC治疗后spamRNA表达增强，静态肺顺应性增加，肺泡灌洗液表面张力特征恢复正常，Ⅱ型细胞板层体恢复至正常形态。

Results After the application of NAC , there exhibited an increase in SPA mRNA expression and static pulmonary compliance , and the restoration of the BAL surface tension to normal .

结论与抗原板法相比，细胞板法检测PRA能更真实反映移植受者体内的抗体情况。

Conclusion Compared with the antigen plate method , the cellular plate method for PRA could be better for the measurement of the antibody level in vivo in pre-transplant recipients .

电镜显示使用Dil后肺泡Ⅱ型细胞板层体较多，微绒毛完整。

After using Dil , there are more lamellar bodies in alveolus cell II and the mini-villuses are complete under the electron microscope .

目的比较抗原板法和细胞板法检测群体反应性抗体（PRA）的差异，探讨其结果与临床实际的相符度。

Objective To compare the difference between antigen plate method and the cellular plate method for panel reaction antigen ( PRA ) assay to explore the consistence with their laboratory results and clinical results .

本文采用酸性磷酸酶（AcPase）电镜组化方法，分别对正常和急性低氧时大鼠肺泡Ⅱ型细胞板层体、溶酶体（多泡体）与GERL进行观察。

The AcPase activity of the lamellar bodies ( LB ), lysosomes and GERLS of type ⅱ alveolar cells were studied in normal and acute hypoxia rats by electron microscopic histochemical technique .

方法采用烟雾吸入性损伤的大鼠模型，观察NAC治疗后spamRNA表达情况，并检测静态肺顺应性、肺泡灌洗液表面张力及Ⅱ型细胞板层体形态。

Methods Wistar rats inflicted with smoke inhalation injury were employed as the model . The expression of SPA mRNA , the static pulmonary compliance , the surface tension of the alveolar lavage and the morphology of lamellae bodies ( LB ) of type ⅱ alveolar cells were examined .

摇床吸附法微量细胞板短期培养快速检测流感病毒

Rapid detection of influenza virus by immunofluorescent staining of shell vial cultures

抗原板法和细胞板法检测群体反应性抗体的比较

Comparison of antigen plate and cellular plate method for panel reaction antigen assay

Ⅱ型上皮细胞板层体急性排空。

Part ⅱ . The lamellar bodies of Type II pneumocytes were evacuated rapidly .

细胞板：植物细胞分裂晚后期出现的一种结构，它和有丝分裂末期新细胞壁的形成有关。

Cell plate A structure that appears in late anaphase in dividing plant cells and is involved in formation of a new cell wall at the telophase stage of mitosis .

分裂末期经成膜体、细胞板产生细胞壁，形成2&细胞花粉。

In telophase a cell wall is produced by the development of a phragmoplast and a cell-plate . Pollen turn into 2-cells , a generative one and a vegetative one .

初始平周壁由自由生长垂周壁分支相接形成，及有丝分裂的细胞板形成。

The initial periclinal walls are formed by the meeting of branches of the freely growing walls and the cell plates . The sporoderm of Sphagnum contains perine , exine and intine .

通过淋巴细胞毒交叉配合试验，12例中，4例（33.3%）温抗体阳性，此4例即为细胞板测定阳性者；

The results of half-micro quality lymphocyte toxic test demonstrated that 4 cases ( 33 . 3 % ) were positive for warm antibody , and these 4 patients were positive for PRA by cellular plate .

事实上体内移植到免疫缺陷性大鼠，LAB可形成含成骨细胞的板层样骨。

In fact , after in vivo transplantation into immunocompromised rats , LAB formed lamellar bone-containing osteocytes .

光、电镜结果提示PS组肺泡大部分复张，Ⅱ型细胞中板层体颗粒有部分释放。

Histological examination of the PS treated lung showed alveolar expansion and partial release of lamellar bodies from type ⅱ epithelium cells .

用纯化的牛FN处理细胞培养板，观察细胞在板中的生长情况，并与在进口板中的生长情况进行比较。

Treat cell culture plate with the extracted FN , observe the growth of cells and compare with that on imported culture plate .

在培养的前中后期，用细胞计数板检测细胞数目，流式细胞仪检测CD34，vWF和eNOS的阳性细胞百分比。

In different culture point , total cells amount , positive percent in CD34 , vWF and eNOS are analysed by FACS .

培养至第12d时的原生质体再生细胞植板率为3.7%。

Protoplast plating efficiency was 3.7 % after 12 days in culture .

所获骨髓种植于细胞培养板内。培养液为含20%胎牛血清DMEM液。

All received are planted in the bone marrow cell culture plates , Mediums are DMEM containing 20 % fetal bovine serum solution .

结果：与C组相比，F、I两组肺泡Ⅱ型细胞内板层体的数量（ND）增多（P0.05），体积（VD）增大（P0.05）；

Results : The amount ( ND ) and volume ( VD ) of lamellar body of type ⅱ alveolar cell in group F and I were increased significantly than that of group C ( P 0.05 ) .

冻存15d后，每组取出1支复苏并接种于细胞培养板培养。

One tube from each group was taken out and inoculated to cell culture board after cryopreserved for 15 days .

此方法在96孔细胞培养板上进行操作，通过GFP检测定量半数病毒复制抑制来替代通过细胞染色定量半数CPE抑制。

This method was carried on 96-well cell culture plate , quantifying the half virus replication reduction by quantifying GFP was used to replace quantifying the half CPE reduction by cell dyeing .

应用紫外分光光度计对光敏剂苯并卟啉衍生物单酸环A（BPD-MA）和细胞培养板盖及培养液的光吸收规律进行了初步观察。

The absorption characteristics of photosensitizer Benzoporphyrin Derivative Monoacid Ring A ( BPD-MA ) and cell culture materials was investigated by UV-2201 ultraviolet spectrophotometer .

该研究旨在探究脂多糖（LPS）诱导的SD幼鼠急性肺损伤时SP-D，SP-dmRNA的时序变化及肺泡Ⅱ型上皮细胞及板层小体的超微结构的变化。

This study was designed to explore the temporal fluctuations of SP-D and SP-D mRNA in young rats with ALI induced by lipopolysaccharide ( LPS ), as well as the alterations of ultrastructures of alveolar type ⅱ( AT ⅱ) cells .

结果老年鼠肺泡Ⅱ型细胞内板层体数为12.20±4.99个/细胞，高于幼年鼠的11.25±3.29个/细胞（P0.01），但低于中年鼠的13.37±4.55个/细胞（P0.05）。

Results The numbers of lamellar bodies in alveolar type ⅱ cells from old rats were 12.20 ± 4.99 per cell , which was higher than that in young ( 11.25 ± 3.29 , P0.01 ) but lower than that in adult rats ( 13.37 ± 4.55 , P0.05 ) .

超微结构Ⅰ组耳蜗Corti器毛细胞皮板下溶酶体改变给药10d较给药5d更明显，可见溶酶体聚集数量增多，体积明显增大；

In GM group , ultrastructural changes of lysosomes beneath cuticular plate of cochlear hair cells were more significant at 10th day than those at 5th day , including the increased number and volume of lysosome .