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MAIN OUTCOME MEASURES: The morphology of BMSCs was observed by the inverted phase contrast microscope. Expression of BMSC surface antigens was detected by flow cytometer. Osteogenous potential was assessed by alkaline phosphatase staining. Adipogenic potential was evaluated by Oil red O staining. Chondrogenic potential was assessed by toluidine blue staining.

主要观察指标:倒置相差显微镜下观察骨髓间充质干细胞的生长状态,流式细胞仪检测细胞表面标志物的表达,采用碱性磷酸酶染色鉴定成骨能力,以油红O染色鉴定成脂能力,以甲苯胺蓝染色鉴定成软骨能力。

MAIN OUTCOME MEASURES: Morphological changes in primary cultured and subcultured mouse BMSCs were measured. BMSC surface antigen of the second passage of mice (CD105, CD44, CD25, CD34) were determined using flow cytometry. The modified method was assessed to harvest the purity of stem cells. Activity of mouse BMSCs was identified using adipogenic and osteoplastic differentiation. The strength of fluorescent cells following multiple passage was observed.

主要观察指标:原代及传代小鼠骨髓间充质干细胞形态变化;对第2代小鼠骨髓间充质干细胞表面抗原,CD105,CD44,CD25,CD34进行流式细胞仪检测,评价改良方法获取干细胞纯度;通过成脂成骨分化,鉴定小鼠骨髓间充质干细胞的活性;观察多次传代后荧光细胞强度。

METHODS: Doppler tissue velocity mode was used and the tricuspid annulus movements of anterior, septal and posterior attachment points in 60 healthy people were detected from apical four chamber view (AP 4CV), parasternal four chamber view (PS 4CV) and apical right heart two chamber view (AP RH 2CV).

应用sequoia 512彩色电脑声像仪,探头型号3V2c,H 3.5 MHz,选用胸骨旁四腔切面(PS 4CV)、心尖四腔切面(AP 4CV)观察60名健康志愿者三尖瓣环前瓣及隔瓣附着点,心尖右心两腔切面(AP RH 2CV)观察三尖瓣环后瓣附着点。

Method]Six intact human cadaver lower extremities were used to produce calcaneal intraarticular fracture models, fracture patterns of the model were observed with radiographical technique, and anatomical study was proceeded to observe the fractures and their effects on soft tissues and compartments in foot.

方法]选用6个新鲜的成人足标本,采用多功能生物力学测定仪建立跟骨关节内骨折模型,通过X线片和CT检查确定骨折的发生并观察骨折的形态,解剖观察骨折的走行及其对足部相关软组织、骨筋膜室的影响。

Method]Six intact human cadaver lower extremities were used to produce calcaneal intra??articular fracture models, fracture patterns of the model were observed with radiographical technique, and anatomical study was proceeded to observe the fractures and their effects on soft tissues and compartments in foot.[Result]All specimens were sustained calcaneal intra-articular fractures successfully, 4 were joint depression fracture in x??

方法]选用6个新鲜的成人足标本,采用多功能生物力学测定仪建立跟骨关节内骨折模型,通过X线片和CT检查确定骨折的发生并观察骨折的形态,解剖观察骨折的走行及其对足部相关软组织、骨筋膜室的影响。

Methods : MTr assay was used to examine the effect of Sorbaria sorbifolia on the proliferation of HepG-2 cell and flow cytometry was used for the cell cycle distribution.

采用MTT比色法观察珍珠梅提取物抑制肝癌HepG-2细胞增殖;采用流式细胞仪检测其对HepG-2细胞周期分布的影响,同时结合倒置显微镜、HE染色、透射电镜及免疫细胞化学方法检测凋亡相关基因bcl-2、p53的蛋白表达,观察其诱导肝癌HepG-2细胞凋亡的作用。

MAIN OUTCOME MEASURES: Differential scanning calorimeter was used to detect thermotical property; polarizing microscope was utilized for the microstructure observation; Antimicrobial activity and slow-release effect were determined by in vitro bacteriostasis and release, respectively.

主要观察指标:差示扫描量热仪表征其热学性能,偏光显微镜观察微观结构;通过体外释放及抑菌实验检测抗菌活性和缓释效果。

Morphology of the EPCs was observed, and the growth curve of the EPCs was investigated. Surface antigens of the EPCs were analyzed by the flow-cytometer. The capability of intaking the acetylated low-density lipoprotein of the EPCs was detected using fluoresencent chemical method. The vasoformative capability and genetic stability of EPCs were cultured in matrigel, and examined by karyotype analysis.

观察培养细胞的形态,测定其生长动力学,采用流式细胞仪及免疫细胞化学方法检测其表型,应用细胞荧光化学法分析EPCs对乙酰化低密度脂蛋白(acetylated low-density lipoprotein, ac-LDL)的摄取功能,Matrigel上培养并检测其形成血管能力,染色体核型分析其遗传稳定性,裸鼠实验、软琼脂实验观察致瘤性。

The ultrasound apparatus is EUB8500, maked by Hitachi, ultrasound probe islinear array probe, 7.5-13.0MHz. After we hocused rats and fixuped them, weexamined rats with probe and forced gently. We controled the strength which keeped3 always and adjust the size of frame, and then observed the color within the frameand blue is electropositive.

将大鼠腹腔麻醉、固定,在超声仪下观察,手持探头轻轻加压,根据仪器指示,使压力始终控制在3左右,调整取样框大小,观察取样框内的颜色变化,蓝色为阳性。

Methods HOS cell line was treated with various concentrations of tretinoin in different durations in vitro. Proliferation suppression was observed by MTT method and invert microscope before and after tretinoin treatment, and protracting cell growth curve. The cell growth and invasion ability was measured with the colony-formation rate in soft agar test.

不同浓度的维甲酸作用HOS细胞,采用噻唑蓝法、倒置相差显微镜观察药物对细胞生长的影响并绘制细胞生长曲线;软琼脂集落形成实验观察细胞生长和侵袭能力的变化;流式细胞仪测定细胞周期变化。

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