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人肾小管上皮细胞HK-2的培养及生长曲线测定 被引量:3

Culturing of Human Tubular Epithelial Cells and Measuring Cell Growth Curve
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摘要 目的:通过细胞计数法绘制人肾小管上皮细胞株HK-2细胞的生长曲线,了解HK-2细胞的生长特性,为相关实验研究提供参考。方法:将HK-2细胞用含10%胎牛血清的DMEM/F12(1∶1)培养基培养,每隔24h在倒置显微镜下观察细胞生长范围,并进行计数,连续观察7d后,以存活细胞数(万/mL)对培养时间(h或d)作图,即得生长曲线。结果:细胞呈立方形铺路石样贴壁生长,细胞间连接紧密。细胞数目在培养第2d开始增加,但在第1~3d增加缓慢,第3~6d细胞数目急剧增加,并进入指数生长期,在第6d时细胞达到饱和密度(100%),在第7d时细胞数目显著下降。结论:在1~3d细胞生长处在潜伏期,3~6d细胞进入大量分裂的指数生长期,第6d达到饱和后,细胞生长则进入衰退期。 Objective:To investigate growth feature of human tubular epithelial cells(HK-2) through cell growth curve. Method:The HK-2 cells were cultured by DMEM / F12(1∶ 1) with 10 % fetal bovine serum. The cells morphology was observed through the microscope,and cells were counted per 24 hours. After observing 7 days the cell growth curve was drawed based on day and amount. Result:We found that HK-2 cells crawling like stone road on the bottle surface. The cell amount began increased on the second day,but the speed was slower during the first day to the third day. The amount increased rapidly from the third day to the sixth day,and the cells were in the exponential phase of growth. On the sixth day,the cells were in saturation density(100% ). However,the amount decreased rapidly on the seventh day. Conclusion:The cells were in the incubation period from the first day to the third day,and in the exponential phase of growth from the third day to the sixth day,and in the decline phase on the seventh day.
出处 《中国实验方剂学杂志》 CAS 北大核心 2010年第10期100-101,105,共3页 Chinese Journal of Experimental Traditional Medical Formulae
基金 科技部国际科技合作项目(2009DFA31520)
关键词 人肾小管上皮细胞 细胞培养 细胞生长曲线 human tubular epithelial cells cell culture cell growth curve
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  • 1Jing-YuanFang Zhong-HuaCheng Ying-XuanChen RongLu LiYang Hong-YinZhu Lun-GenLu.Expression of Dnmt1,demethylase,MeCP2 and methylation of tumor-related genes in human gastric cancer[J].World Journal of Gastroenterology,2004,10(23):3394-3398. 被引量:19
  • 2Xiao-UXu,JianYu,Hong-YuZhang,Meng-HongSun,JunGu,XiangDu,Da-RenShi,PengWang,Zhen-HuaYang,Jing-DeZhu.Methylation profile of the promoter CpG islands of 31 genes that may contribute to colorectal carcinogenesis[J].World Journal of Gastroenterology,2004,10(23):3441-3454. 被引量:43
  • 3崔晶,翟光喜,娄红祥.姜黄素的研究进展[J].中南药学,2005,3(2):108-111. 被引量:58
  • 4刘海军,刘丽秋,于俊生.肾间质纤维化的发生机制及其中药防治进展[J].中国中西医结合肾病杂志,2005,6(11):677-680. 被引量:14
  • 5XU J, FU Y, CHEN A. Activation of peroxisome proliferator-activated receptor-gamma contributes to the inhibitory effects of curcumin on rat hepatic stellate cell growth [ J ]. Am J Physiol Gastrointest Liver Physiol, 2003, 285 ( 1 ) : 20 - 30.
  • 6ZHENG S, CHEN A. Activation of PPAR gamma is required for curcumin to induce apoptosis and to inhibit the expression of extracellular matrix genes in hepatic stellate cells in vitro [J]. Biochen,2004, 384 (1) : 149 - 157.
  • 7PUNITHA VA THI D, VENKATESAN N, BABU M, et al. Protective effects of curcumin against amiodarone-induced pulmonary fibrosis in rats [J]. Br J Pharmacol,2003, 139 (7) : 1342 - 1350.
  • 8GAEDEKE J, NOBLE N A, BORDER W A. Curcumin blocks multiple sites of the TGF-beta signaling cascade in renal cells [J]. Kidney Int,2004, 66 (1) : 112 - 120.
  • 9EGAN M E, PEARSON M, WEINER S A, et al. Curcumin, a major constituent of turmeric, corrects cystic fibrosis defects [J]. Science,2004, 304 (5670): 600-602.
  • 10TAKASHI WASA, HITOSHI YOLOMAMA, KOUJI MATSUSHIMA. Chemokines in renal disease [ J]. International Immunophamacology, 2001:637-645.

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  • 1刘红亮,王靖凯,邓锦波,胡磊,张路,刘彬.Fluoro-Jade B染色与TUNEL比较检测乙醇诱导神经细胞凋亡[J].解剖学杂志,2014,0(3):356-359. 被引量:1
  • 2于建宁,苗德强,马所峰,谭秀文,袁继红,谭景和.影响小鼠体细胞脂质体法转染效率的因素[J].实验生物学报,2005,38(5):404-410. 被引量:8
  • 3Kim T K, James H E. Mammalian cell transfection: the present and the future. Analytical and Bioanalytical Chemistry, 2010, 8(397): 3173-3178.
  • 4Park K W, Lai L, Cheong H T, Cabot R, Sun Q Y, Wu G, Rucker E B, Qurtschi D, Bonk A, Samuel M, Rieke A, Day B N, Murphy C N, Carter D B, Parther R S. Mosaic gene expression in nuclear transfer-derived embryos and the production of cloned transgenic pigs from ear-derived fibroblasts. Biology of Reproduction, 2002, 66(4): 1001-1005.
  • 5Bordignon V, Keyston R, Lazaris A, Bilodeau A S, Pontes J H, Amold D, Fecteau G, Keefer C, Smith L C. Transgene expression of green fluorescent protein and germ line transmission in cloned calves derived from in vitro-transfected somatic cells. Biology of Reproduction, 2003, 68(6): 2013-2023.
  • 6Watanabe S, Iamoto M, Suzuki S, Fuchimoto D, Honma D, Nagai T, Hashimoto M, Yazaki S, Sato M, Onishi A. A novel method for the production of transgenic cloned pigs: electroporation-mediated gene transfer to non-cultured cells and subsequent selection with puromycin. Biology of Reproduction, 2005, 72(2): 309-315.
  • 7Takahashi K, Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell, 2006, 126(4): 663-676.
  • 8Okita K, Nakagawa M, Hyenjong H, LChisaka T, Yamanaka S. Generation of mouse induced pluripotent stem cells without viral vectors. Science, 2008, 322(5903): 949-953.
  • 9Lesage D, Cao A, Briane D, Lievre N, Coudert R, Raphael M, Salzmann J I, Taillandier E. Evaluation and optimization of DNA delivery into gliosarcoma 9L cells by a cholesterol-based cationic liposome. Biochimica et Biophysica Acta, 2002, 1564(2): 393-402.
  • 10Ross J W, Whyte J J, Zhao J, Samuel M, Wells K D, Prather R S. Optimization of square-wave electroporation for transfection of porcine fetal fibroblasts. Transgenic Research August, 2010, 19(4): 611-620.

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