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Following 72 h co-culture, desquamate, sporozoites, trophozoites, meronts, microgametocytes, macrogametocytes, zygote, thin-wall oocyst, and thick-wall oocyst appeared orderly. Between the 60th and 72th hour, many oocysts emerged. Inoculated by the C. parvum -infected cell culture supernatant at the 48th hour, the immunosuppressed mice became infected.

在感染后72 h内,隐孢子虫出现连续发育阶段,包括脱囊、子孢子、裂殖子、裂殖体、滋养体、配子体、合子、薄壁卵囊和厚壁卵囊,在60~72 h内形成卵囊;用感染48 h的细胞培养上清接种于免疫抑制小鼠, 10 d后有隐孢子虫卵囊排出。

This paper reviewed the research progresses about the cysts, especially the resting cysts of protozoans, mainly focused on the characteristics of morphologies, structures, constituents, and living activities, as well as molecular mechanism and significance of encystment for the protozoans, also, cell behavior during encystment and excystment was involved based on the references reported.

以国内外文献报道为依据,综述了原生动物包囊,特别是休眠包囊的研究进展情况,主要集中在包囊的形态、结构、组成、生命活动特征、包囊形成的分子作用机理和意义,以及包囊形成与解脱过程中细胞行为上的研究等方面。

In 1988 a lacrimal gland tumor was incompletely removed from the left orbit of a 36-year-old woman and diagnosed as "solid basaloid adenoid cystic carcinoma". Soon after, an exenteration of the orbit was performed. In 1998, upon review of the initial histopathology, the diagnosis of solid adenoid cystic carcinoma was changed to basal cell adenocarcinoma..

方法;1988年一个36岁的妇女的泪腺肿瘤从左眼眶不完全摘除,诊断为"实质性基底细胞囊腺癌",不久进行了眼眶内容去除术。1998年对原始的组织病理学进行回顾,实质性基底细胞囊腺癌被更正为基底细胞腺癌。

In resting cysts, the microtubules under the pellicle, cortical ciliatures, conjunctions between cilia basal bodies, supporting structure of basal bodies and other microtubule structures are absorbed in different extent; microtubule-like assemble bodies appear at the center of the remained cilia basal bodies; the granules of chromatin and nucleolus in macronucleus become smaller whereas nucleus pores of the micronucleus become bigger; the inner membrane of some nucleus pores are attached with chromatin.

结果表明:纤毛虫形成包囊过程中,皮层细胞质中产生具有自噬泡消化特征的细胞器,将部分纤毛结构等逐步消化;休眠包囊中,表膜下微管、皮层纤毛器和纤毛基体间连接、基体托架及其他微管结构不同程度地被吸收、在残剩纤毛基体的中央形成微管形结构聚合体,大核染色质和核仁颗粒变小,核孔增大,并发生染色质附着于核孔内膜的现象;细胞脱包囊期间,皮层细胞骨架、线粒体等经历了在残剩结构基础上的再分化。

Results coculture with endometrial epithelial cells could promote the formation of mouse morula (71.3% and 61.2%,p.05) and blastocyst (50.0% and 39.7%,p.05), and increase the blastocyst hatched rate (34.8% and 24.3%,p.05) and total cell number of blastocyst (44.1 and 35.6, p.05).conclusion coculture with endometrial epithelial cells can facilitate the development of early mouse embryo in vitro, which can optimize the condition of embryonic development in vitro.

结果:与无上皮细胞相比,共培养明显促进了小鼠桑椹胚率(71.3%和61.2%,p.05),囊胚率(50.0%和39.7%,p.05),囊胚孵化率(34.8%和24.3%,p.05)和胚胎总细胞数(44.1和35.6,p.05)。结论:子宫内膜上皮细胞能够促进小鼠胚胎的体外发育,对早期胚胎的体外发育环境具有优化作用。

These observations show that reprogramming is easier in interspecific embryos reconstructed with ES cells than that reconstructed with somatic cells, and that ES cells have the higher ability to direct the reconstructed embryo development normally than fibroblast cells. Oocytes were reconstructed with outbreeding Kunming albino mouse ES cells and enucleated rabbit oocytes, and the effects of the passages of ES cells and 6-DMAP on the development of interspecific reconstructed oocytes were analyzed. The interspecific reconstructed ES-rabbit oocytes were activated either by combined two set electric pulses and 6-DMAP or by two set electr

以上结果显示,6-DMAP能增加胚胎干细胞异种重构卵的卵裂率,对重构卵囊胚的发育率影响不大;高培养代数和低培养代数的胚胎干细胞用于异种核移植不影响异种重构卵的卵裂率和囊胚发育率;用胚胎干细胞作为供核细胞;比体细胞作为供核细胞所构建的异种重构胚更容易进行重编程,并且胚胎于细胞指导异种克隆胚胎正常发育的能力强于体细胞。

A core needle biopsy misdiagnosed PASH in 13 cases out of 28 cases and vacuum-assisted biopsy correctly identified PASH in all 3 cases.

4细胞性纤维腺瘤和囊肉瘤:PASH缺乏真正的间叶细胞过生长的现象,其细胞缺乏多形性,无核分裂象,也没有纤维腺瘤或囊肉瘤的上皮成分的生长类型。

Methods Neomycin was used to destroy guinea pig utricular hair cells in vitro.The culture in experimental groups was supplemented with bFGF.The culture in control group was not supplemented with bFGF.All utricles were observed by scanning electronic microscope,and the number of survival utricular hair cells was accounted.

采用离体的豚鼠椭圆囊培养法,对照组为普通前庭培养液培养,实验组按培养液中含和不含bFGF分组,用新霉素造成各实验组培养的椭圆囊毛细胞损伤,各组椭圆囊均行扫描电镜检查并行毛细胞计数。

The LBL self-assembly process was monitored by flow cytometry and zeta potential analyzer. Scanning electron microscope, dynamic light scattering, and flow cytometry were used to characterize microcapsules The microcapsules were 1.14 μm in size and stable in lyophilizing.

在微囊的制备过程中,采用流式细胞仪和Zeta电位仪对层层自组装进行监测,并对制得的微囊采用扫描电子显微镜、动态光散射仪、流式细胞仪等进行表征,结果发现微囊的直径在1微米左右,尺寸较均一。

This experiment object was 1-cell embryo of KUNMING mouse , ROS was added in different developmental phases through basal medium with CZB medium, cultured to morulae, early blastula, blastula and the hatching of blastula, observed the change of cell number and cleavage index of embryo.

本试验以昆明小鼠1-细胞期胚胎为实验对象,以CZB培养液为基础液在不同发育阶段添加外源性ROS,培养至桑椹胚、早期囊胚、囊胚、扩张囊胚阶段,分别观察胚胎的胚细胞数、分裂指数的变化。

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