线粒体

On the membrane of liver parenchymal cell and endothelial cell ×12 000;Fig 4 3 h after Cd-injection:ER extremely dilatant,mitochondria swollen,a lot of Ce-H2O2 precipitation on the membrane of PC,EC and Kupffer＇scell ×15 000;Fig 5 6 h after Cd-injection:in irreversible state,hepato-cytoplasm clear,few organelle,a few Ce-H2O2 precipitation on the membrane of PC and eC ×5 500;Fig 6 24 h after Cd-injection:hepatocyte plasmotorrhexis,membrane of

ce呈点状沉积在肝实质细胞、内皮细胞膜上×12 000；图4 染镉后3小时：ER极度扩张，线粒体膨胀，内外膜模糊不清；见大量Ce沉积在PC、EC和Kupffer＇s细胞膜上×15 000；图5 染镉后6小时：处于不可逆改变状态的肝细胞胞浆清亮，少有细胞器；仍可见少量Ce沉积在PC和EC膜上×5 500；图6 染镉后24小时：可见破碎的肝细胞，胞内膜结构大多已不清晰；未见Ce的沉积×7 000

Dimerization interactions of Bcl-2 family proteins regulate mitochondrial and other intracellular organelle function.

Bcl-2蛋白家族通过二聚体的形成在调节线粒体及其它细胞器的功能方面起着重要作用。

The present studies showed that two cell populations were found in haemocytes: large cell with high granularity and small cell with low granularity by flow cytometry FCM on light scanttering pattern. Two distinct cell types were identified based on phase contrast microscope: one type of cell was dark and dioptric aberration, while the other was bright and dioptric strong. By Giemsa and H.E staining, cytoplasmic staining were heterogeneous and internal particles were obvious in one type of cell, while cytoplastic staining were homogeneous and internal particles were inexistent in the other type of cell. By transmission electron microscope, we found that the mitochondria, Golgi apparatus organelles were rich and internal particles were obvious in one type of cells, and contrary to the another cells.

流式细胞术光散射图谱显示血细胞被分两类，一类为颗粒度高的大细胞，另外一类为颗粒度低的小细胞；相差显微镜观察显示，血细胞可分为胞体暗、折光性差和胞体明亮、折光性强的两类； Giemsa和H.E染色显示细胞分为胞质染色不均一、胞内颗粒明显和胞质染色均一、胞内颗粒不明显的两类；透射电镜超薄切片观察显示，颗粒明显的细胞胞质内线粒体、高尔基体等细胞器较丰富，颗粒不明显的细胞胞质内细胞器较少；负染结果表明血细胞主要分为表面不光滑、突起明显和细胞表面光滑、突起较不明显的两类。

The maximal binding content and the dissociation constant were determined from Scatchard plot. The mRNA and protein expressions of UCP4 and UCP5 were measured by RT-PCR and Western blot, respectively.

结果显示，1 mmol/L GDP可降低体外大鼠脑组织线粒体中UCPs与[3H]-GTP结合的Bmax，提高Kd，但对脑组织中UCP4和UCP5 mRNA和蛋白表达量的改变无统计学意义。

Partial mitochondrial cytochrome oxidase Iregion was sequenced from 37 individuals of sterile males and wild males of Bactrocera dorsalis (Hende1) from 7 different regions of Fujian Province.

对橘小实蝇不育雄虫和福建7个不同地区的野生雄虫共37个个体的线粒体细胞色素氧化酶I基因进行了部分序列测定。

In type 2 diabetic rats, there is renal mitochondrial dysfunction which contributes to the development of diabetic nephropathy.

2型糖尿病大鼠肾脏存在明显的线粒体功能障碍，此与肾病的发生和发展有关。

The Ndrg2 protein localize in the cytoplasm of many cell lines; in normal conditions, the Ndrg2 protein may colocalize with mitochondria; both of endogenous and ectogenesis Ndrg2 can translocate from the cytoplasm to the nucleus in the conditions of hyposia stress; a new splicing variant of NDRG2 may exist.

Ndrg2在多种细胞系中均定位于细胞质；未给予任何刺激时Ndrg2与线粒体可能有共定位；内源性及外源性Ndrg2在模拟低氧刺激条件下可发生核转位。

Involvement of p53 and Bcl-2 family proteins in regulating programmed cell death and proliferation in human embryogenesis.

Bcl-2，Bax和线粒体膜蛋白在一氧化氮供体诱导HL-60细胞凋亡中的改变。

Endo G and AIF both are mitochondrial proteins.

Endo G和AIF都是线粒体蛋白。

OVCs were isolated by density ladder centrifugation in the 4th week, and then OVC's morphology was observed under transmission electromicroscrope and immunocytochemistry were performed to detect the expression of ICAM-1. Results Observing OVC's morphology under transmission electromicroscrope showed that OVC was infantile and undifferentiated with big nucleus, clear nucleolus, large nucleoplasm-ratio, small mitochondria, and little endoplast.

结果 透射电镜下观察到OVCs超微结构的改变为核大，核/浆比大，核仁小，胞浆内细胞器少，可见少量内质网和小线粒体，整个细胞呈幼稚、未分化状态；ICAM-1免疫细胞化学检测阳性；损伤肝组织HE染色和ICAM-1免疫组化检测显示，肝损伤初期，Hering管周围OVCs增生并且ICAM-1阳性表达，随着肝损伤的加重，OVCs继续增生，并且，OVCs沿增生的肝纤维向肝小叶迁移，同时，ICAM-1阳性表达也继续增多，并逐渐向肝小叶弥散分布；透射电镜下观察到，肝损伤初期，OVCs在Hering管周围增生，肝纤维随之增生，增生的OVCs与肝纤维黏附生长。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。