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RESULTS摘要: Otocyst cells differentiated and proliferated and showed several morphotypes, mainly including epitheliallike cells, fibroblastlike and neuronlike cells.

结果摘要:培养的细胞在体外进行分化和增殖,细胞形态主要有上皮细胞形态、成纤维细胞形态和神经细胞形态3种。

METHODS: Otocyst epithelia surgically isolated from fetal rats were cultured and passaged. Proliferation and differentiation of cultured cells were observed using BrdU labeling to find the progenitors. Immunocytochemistry (Factin, cytokeratin and calretinin) was used to detect cell properties of cultured cells.

取孕鼠胚胎听囊细胞进行体外培养,用免疫细胞化学方法,分别对培养的细胞进行细胞角蛋白、F肌动蛋白和calretinin染色观察细胞特征;BrdU染色观察细胞增殖。

METHODS摘要: Otocyst epithelia surgically isolated from fetal rats were cultured and passaged. Proliferation and differentiation of cultured cells were observed using BrdU labeling to find the progenitors. Immunocytochemistry (Factin, cytokeratin and calretinin) was used to detect cell properties of cultured cells.

方法摘要:取孕鼠胚胎听囊细胞进行体外培养,用免疫细胞化学方法,分别对培养的细胞进行细胞角蛋白、F肌动蛋白和calretinin染色观察细胞特征;BrdU染色观察细胞增殖。

Objective To investigate the effects of oxidative stress on the proliferation of rat hepatic stellate cells.

目的 探讨H2S对大鼠肝星形细胞增殖和氧应激的影响。

The overall effectiveness of NPDR was 85.0%, the overall effectiveness of PDR was 82.4%.

9治疗两个月后单纯型组与增殖型组总体疗效的有效率分别是85.0%、82.4%。

ABSTRACT] Objective To investigate the effect of calcitonin generelated peptide on the proliferation and apoptosis of HaCaT cells.

目的 探讨降钙素基因相关肽对HaCaT 细胞增殖、凋亡的影响。

HepG 2 cell line was treated with the pharmaceutic serum at different conˉcentrations for24h and48h respectively.

文献法制备豆楮方含药血清,用MTT法观察药物作用24h、48h后细胞的增殖情况。

WM can inhibit proliferation and induce apoptosis of K562 cells in a dose- and time-dependent manner, probably through down-regulation of phosphorate PI3K/Akt signal pathway and NF-κB expression.

渥曼青霉素以时间和剂量依赖方式明显抑制K562细胞的增殖及诱导其凋亡,其机制可能与其下调磷酸化PI3K/Akt信号通路以及NF-κB蛋白表达有关。

Phycocyanin could not change the level of integin β1 expression.

不同浓度藻蓝蛋白对K562细胞的增殖均有抑制作用。

Cellular analysis demonstrated that PIKA elicited the activation and proliferation of B cells and NK cells but not CD4+ and CD8+T cells.

细胞亚群分析的结果表明,PIKA可显著刺激B细胞和NK细胞活化、增殖。

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