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赛替派诱导人支气管上皮细胞恶性转化过程中不同形态集落来源细胞的研究 被引量:1

The Cell Strains Derived from Different Morphologic Colonie s in the Process of Malignant Transformation of Human Bronchial Epithelial Cells by Thiotepa
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摘要 背景与目的:研究赛替派转化人支气管上皮细胞株(Humanbronchialepithelialcellstrain2B,BEAS-2B)过程中两种不同形态集落来源的细胞株的细胞构成和成瘤性的变化情况。材料与方法:赛替派转化BEAS-2B细胞过程中产生两种形态学上差异明显的集落,对其分离培养,细胞建株,分别命名为BEAS-S(HumanbronchialepithelialcellstrainS)和BEAS-C(HumanbronchialepithelialcellstrainC)细胞,连续传代,同时通过特异免疫细胞化学染色了解细胞构成的改变,结合细胞凝集性和锚着独立性的变化进行分析。结果:BEAS-C细胞随着传代,基底细胞标志物质蛋白34βE12表达增强,同时其细胞凝集性和成瘤性也增强;而BEAS-2B和BEAS-S细胞的细胞构成及成瘤性在传代过程中改变不明显。结论:基底细胞可能是人支气管上皮细胞恶性转化的干细胞,同时两种细胞集落形态的差异性也为人源细胞转化的形态学研究提供参考价值。 BACKGROUND&AIM: To study the changes of cellulosity and tumorigenicity of the two cell strains derived from different morphologic colonies in the process of malignant transformation of human bronchial epithelial cell strain2B(BEAS-2B)treated with thiotepa. MATERIAL AND METHODS: The two different morphologic colonies,which derived from transformed BEAS-2B cells by thiotepa,were isolated and cultivated respectively.We established the two cell strains and named them human bronchial epithelial cell strain S(BEAS-S)and human bronchial epithelial cell strain C(BEAS-C).With the passage,the immunocytochemistry stain,cellular agglutination test and anchorage independence test were used to analyze their changes of cellulosity and tumorigenicity. RESULTS: With the passage,the basal cell's special marker cytokeration34βE12express increased in BEAS-C cells as its cellular agglutination and tumorigenicity,but these don't change obviously in the BEAS-2B cells and BEAS-S cells. CONCLUSION: The basal cell might be the stem cell of malignant transformation of human bronchial epithelial cells.Meanwhile,the morphometric difference of these cells and colonies provided valuable information to the morphometrig research of transformation of human-originated cells.
出处 《癌变.畸变.突变》 CAS CSCD 2005年第4期198-201,共4页 Carcinogenesis,Teratogenesis & Mutagenesis
基金 国家自然科学基金资助(No.30271559)
关键词 赛替派 永生化人支气管上皮细胞 恶性转化 形态计量学 免疫细胞化学染色 thiotepa immortalized human bronchial epithelial cells malignant transformation morphometry immunocytochemistry stain
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参考文献10

  • 1IARC. Thiotepa study in pharmaceutical drugs[C]. Lyon: IARC Scientific Publications. 1990, 50:123 - 141. 被引量:1
  • 2Reddel RR,Gerwin BI,McMenamin MG,et al . Transformation of human bronchial epithelial cells by infection with SV40 or adenovirus-12 SV40 hybrid virus, or transfection via strontium phosphate coprecipitation with a plasmid containing SV40 early region genes[J]. Cancer Res, 1988,48(7): 1 904- 1 909. 被引量:1
  • 3Boers JE, Ambergen AW, Thunnissen FB. Number and proliferation of basal and parabasal cells in normal human airway epithelium[J]. AM J Respir Crit Care Med, 1998, 157:2000-2006. 被引量:1
  • 4Boers JE, Den Brok JLM, Koudstaal J, et al. Number and proliferation of neuroendocrine cells in normal human airway epithelium[J]. AM J Respir Crit Care Med, 1996, 154:758 - 763. 被引量:1
  • 5黄建民,何韶衡,赵卫华.气道粘液、粘蛋白及其分泌调节[J].中国病理生理杂志,2003,19(9):1267-1271. 被引量:12
  • 6孙秀泓,罗自强主编..肺的非呼吸功能基础与临床[M].北京:人民卫生出版社,2003:381.
  • 7Boers JE, Ambergen AW, Thunnissen FB. Number and proliferation of Clara cells in normal human airway epithelium[J] .AM J Respir Crit Care Med, 1999, 159:1 585 - 1 591. 被引量:1
  • 8Soderberg M. Structural characterization of bronchial mucosal biopsies from healthy volunteers: A light and electron microscopical study[J]. Eur Respir J, 1990,3:261. 被引量:1
  • 9张煦,赵俊生.肺癌组织学类型的光镜、电镜比较观察[J].兰州大学学报(自然科学版),1998,34(1):85-89. 被引量:1
  • 10IARC/NCI/TEPA Working Group. Cellular and molecular mechanisms of cell transformation assays of established cell lines for prediction of carcinogenic chemicals[J]. Cancer Res,1985,45(1):2 395-2 399. 被引量:1

二级参考文献31

  • 1Takeyama K, Jung B, Shim J J, et al. Activation of epidermal growth factor receptors is responsible for mucin synthesis induced by cigarette smoke[J]. Am J Physiol Lung Cell Mol Physiol, 2001, 280(1): L165-L172. 被引量:1
  • 2Wang H, Liu X, Umino T, et al. Cigarette smoke inhibits human bronchial epithelial cell repair processes [ J ]. Am J Respir Cell Mol Biol, 2001, 25(6) : 772 - 779. 被引量:1
  • 3Yanagihara K, Seki M, Cheng PW. Lipopolysaccharide induces mucus cell metaplasia in mouse lung[ J ]. Am J Respir Cell Mol Biol, 2001, 24(1): 66-73. 被引量:1
  • 4Li JD, Feng W, Gallup M, et al. Activation of NF- kappaB via a Src- dependent Ras- MAPK- pp9Orsk pathway is required for Pseudomonas aeruginosa - induced mucin overproduction in epithelial cells[J]. Proc Natl Acad Sci USA,1998, 95(10) : 5718- 5723. 被引量:1
  • 5Kim YD, Kwon EJ, Kwon TK, et al. Regulation of IL-1beta-mediated MUC2 gene in NCI-H292 human airway epithelial cells[J].Biochem Biophys Res commun,2000,274(1):112-116 被引量:1
  • 6Temann UA, Prasad B, Gallup MW, et al. A novel role for murine IL- 4 in vivo : induction of MUCSAC gene expression and mucin hypersecretion [ J ]. Am J Respir Cell Mol Biol,1997, 16(4) : 471 - 478. 被引量:1
  • 7l_ouahed J, Toda M, Jen J, et al. Interleukin- 9 upregulates mucus expression in the airways[J]. Am J Respir Cell Mol Biol, 2000, 22(6): 649-656. 被引量:1
  • 8Shim JJ, Dabbagh K, Ueki IF, et al. IL- 13 induces mucin production by stimMating epidermal growth factor receptors and by activating neutrophils[J]. Am J Physiol Lung Cell Mol Physiol, 2001, 280( 1 ) : L134 - L140. 被引量:1
  • 9Fischer BM, Rochelle I.G, Voynow JA, et al. Tumor necrosis factor- alpha stimulates mucin secretion and cyclic GMP production by guinea pig tracheal epithelial cells in vitro[J]. AmJ Respir Cell Mol Biol, 1999, 20(3): 413-422. 被引量:1
  • 10Takeyama K, Dabbagh K, Lee HM, et al. Epidermal growth factor system regulates mucin production in airways[J]. Proc Natl Acad Sci USA, 1999, 96(6) : 3081 - 3086. 被引量:1

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