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纤维细胞

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IntroductionBasic fibroblast growth factor is a kind of cell growth factor which has a great effect on proliferation and differentiation to mesodermic cells.

前言 碱性成纤维细胞生长因子是一种对中胚层来源的细胞有强烈促增殖和分化作用的细胞生长因子。

Marrow stromal cell ; fibrin sealant ; cell culture ; bone morphogenic protein ; basic fibroblast growth factor

骨髓基质细胞;纤维蛋白胶;细胞培养;骨形态发生蛋白2;碱性成纤维细胞生长因子

Control group: inflammatory cell infiltration (1W); inflammatory cell disappearance, fibroblast and capillary tachyauxesis (2W); osteoblast appearance around bone defect (1M); small amount neoformative bone tissue around bone defect.

对照组:术后1周,骨缺损区周围有大量炎性细胞浸润;术后2周,炎性渗出吸收,成纤维细胞、毛细血管生长活跃;术后1个月,骨缺损区周围有成骨细胞;术后3个月,骨缺损边缘有少量新骨沉积。

Control group: inflammatory cell infiltration (1W); inflammatory cell disappearance, fibroblast and capillary tachyauxesis (2W); osteoblast appearance around bone defect (1M); small amount neoformative bone tissue around bone defect. Conclusion TGF-β1 can induce alveolar bone regeneration.

对照组:术后1周,骨缺损区周围有大量炎性细胞浸润;术后2周,炎性渗出吸收,成纤维细胞、毛细血管生长活跃;术后1个月,骨缺损区周围有成骨细胞;术后3个月,骨缺损边缘有少量新骨沉积。

These nonmalignant cells, such as stromal fibroblasts and bone marrow-derived cells, have been shown to be capable of promoting tumor growth and metastasis.

这些非恶性细胞如基质成纤维细胞和骨髓源性细胞已被证明能够促进肿瘤的生长和转移。

Immunohistochemistry was positive for VIM in a large fraction of fibrocytes, vascular endothelial cells, vessel wall and perithelial cells.

波形纤维蛋白免疫组织化学染色在大部分纤维细胞、血管内皮细胞、血管壁及周细胞呈阳性反应。

The cells were shammed or irradiated with different dosages of UVB radiation and treated with the above TCM monomers. The damage of fibroblasts was observed with inverted phase contrast microscope.Cellular proliferation activity was detected by MTT method.The secretory volume of IL-6 and TNF-α was measured by ELISE. Results The damage degree of the cells irradiated was dependent with the irradiated doses and the proliferation activity reduced by 28%-44%.

采用30mJ/cm^2、60mJ/cm^2、90mJ/cm^2剂量UVB照射体外培养的原代人皮肤成纤维细胞,以中药单体EGCG和黄芩苷进行干预处理,倒置相差显微镜观察细胞受损程度,以甲唑盐比色试验检测细胞增殖活性,酶联免疫吸附试验检测上清液TNF-α、IL-6分泌量。

Methods The cells of LLC-PK1,Hela,Caki-1,T24 and fibroblast were incubated on 96-w ell plate with addition of diffe-rent concentration of cystic fluid of ACDK and t hat of simple renal cyst. After 24 hours for reaction, MTT method was used to de termine and compare the proliferative activity of 5 cell lines.

将LLC-PK1, Hela, T24, Caki-1和成纤维细胞接种于96孔培养板中,经过24h培养,加入不同浓度的ACDK和单纯肾囊肿的囊内液作用24h,用MTT法测定培养细胞的增殖活性,比较两者之间对细胞增殖的抑制作用。

The proliferation of cultured rat renal fibroblasts was measured by means of methylthio tetrazole method.

用重组PTEN腺病毒转染体外培养大鼠肾成纤维细胞,MTT法检测细胞增殖活力,免疫细胞化学检测PCNA蛋白表达。

Results: Under the compression with a magnitude of 15KP、 30KP, the proliferation of HPDLFs greatly increased, and the percentage of the content of DNA of cells in S phase increased tooP

结果:①。OKP、15KP、30KP、45KP的持续性静压力,加力1小时后,体外培养的人牙周膜成纤维细胞增殖活性的变化为:0~15~30KP,增殖指数以及S期细胞DNA百分比都显著增高(P<0.05);45KP压力下,增殖指数及S期细胞DNA百分比明显降低。②。

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The relationship between communicative competence and grammar teaching should be that of the ends and the means.

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