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肠上皮内淋巴细胞促L929细胞增殖活性的研究 被引量:2

Effects of conditioned supernatants from intestinal intraepithelial lymphocytes on the proliferation of L929 cell line in mice with stress ulcer
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摘要 目的:了解应激性溃疡模型中肠上皮内淋巴细胞(iIEL)培养上清促L929细胞增殖活性的变化。方法:采用水浸限制刺激法制备小鼠应激性溃疡模型。分别提取iIEL和脾T淋巴细胞,在含ConA的培养液中培养。采用MTT法检测iIEL和脾T淋巴细胞培养上清的促L929细胞增殖活性。结果:正常鼠iIEL培养上清促L929细胞增殖活性显著高于脾T细胞培养上清(P<0.05)。应激性溃疡发生后,iIEL培养上清促L929细胞增殖活性显著下降,于第4天降至最低(P<0.05),1周后恢复正常。结论:iIEL培养上清中可能含有高水平的促进L929细胞增殖的因子,这种因子的活性在应激性溃疡中可能发生变化。 Objective: To invcstigate the effects of conditioned supernatants from intestinal intraepithelial lymphocytes (iIEL) on the proliferation of L929 cell line in mice with stress ulcer. Methods: Mouse models of stress ulcer were made by using water-immersion restraint stress, iIEL and splenic T lymphocytes were isolated and cultured by ConA, Conditioned supematants were obtained from the cultures of ilEL. The proliferation rate of L929 cells was measured by MTT method. Results: The proliferation rate of L929 cell in the iIEL-conditioned culture medium was significantly higher than that in the splenic T cell-conditioned cuhure medium in the normal control mice ( P 〈 0.05 ). The promoting effect of ilEL-conditioned supernatants on the proliferation of L929 cell decreased after stress ulcer was induced, reaching the lowest level on the fourth day ( P 〈 0.05 ) , and returned to normal a week later. Conclusion: The conditioned supematants of iIEL may contain factors which may have positive effect on the proliferation of L929 cell line, and the activity of these factors may change in the stress ulcer.
出处 《中国医科大学学报》 CAS CSCD 北大核心 2005年第4期292-293,296,共3页 Journal of China Medical University
基金 国家自然科学基金资助项目(39600133)
关键词 畅上皮内淋巴细胞 L929细胞 应激性溃疡 intestinal intraepithelial lymphoeytes L929 cell line stress ulcer
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  • 1陈丙莺,马建吟,黄钦田,尤丽芬.简易自然杀伤试验——LDH释放改良法[J].上海免疫学杂志,1989,9(4):218-219. 被引量:104
  • 2陈佰义,姜莉,赵洪文,吕长俊,侯显明.博莱霉素致大鼠肺纤维化肺泡巨噬细胞氧化和抗氧化损伤的动态研究[J].中国医科大学学报,1995,24(3):240-242. 被引量:17
  • 3石川博通.消化管IEL细胞分化.Medical Immunology,1993.25(3):209-212.
  • 4Beagtey KW, Musband AJ. lntraepithelial lymphocytes: origins, distribution and function. Crit Rev Immunol, 1998, 18(3): 237-241.
  • 5Tan Z, Nagata S. PVN c-fos expression, HPA axis response and immune cell distribution during restraint stress. JUOEH, 2002, 24(2) : 131-149.
  • 6Sambrook J, Fritsch EF, Maniatis T. Molecular Cloning, A Laboratory Manual. 2nd ed, Cold Spring Harbor Laboratory, 1989, 8:46-52.
  • 7Mattapallil JJ, Reay E, Dandekar S, et al. An early expansion of CD8 alpha beta T ceils, but depletion of rididant CD8 alpha alpha T cells, occurs in the intestinal epithelium during primary simian immunodeficiancy burus infection. AIDS, 2000, 14(6): 637-646.
  • 8Matrumoto S, Nanno M, Watanabe N, et al. Physiological roles of gamma delta T-cell receptor intraepithelial lymphocytes in cytoproliferation and differentiation of mouse intestinal epithelial cells. Immunology, 1999, 97(1): 18-25.
  • 9Guy GD, Disanto JP, Menchoz P, et al. Small bowel enteropathy, role of intraepithelial lymphocyteses and of cytokines (IL-12, IFN-7, TNF-a) in the induction of epithelial cell death and renewal. Ear J lmmmunol, 1998,28(2):730-735.
  • 10Hirose K, Suzuki T, Nishimura H, etal. Interleukinn-15 may be responsible for early activation of intestinal intraepithelial lymphocytes after oral infection with Listeria monocytogenes in rats. Infect Immunol, 1998, 66(12) : 5677-5683.

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  • 1王莉,张伟京.肿瘤热疗与免疫治疗[J].国际肿瘤学杂志,2006,33(5):357-360. 被引量:7
  • 2Borchmann P, Schnell R, Engert A. Immunotherapy of Hodgkin' s lymphoma[ J]. Eur J Haematol, 2005 ; 75 (Suppl 66) : 159-165.
  • 3Hainsworth J D, Litchy S, Burris H A 3rd et al. Rituximab as first-line and maintenance therapy for patients with indolent non-Hodgkin's lymphoma[ J ]. J Clin Oncol, 2002 ; 20(20 ) : 4261-4267.
  • 4Schnell R, Borchmann P, Staak J O et al. Clinical evaluation of riein Achain immunotoxins in patients with Hodgkin' s lymphoma [ J ]. Ann Oncol, 2003 ; 14 (5) : 729-736.
  • 5ZeisM, Siegel S, Wagner A et al. Generation of cytotoxic responses in mice and human individuals against hematological malignancies using survivin-RNA-transfected dendritic cells [ J ]. J Immunol, 2003 ; 170 ( 11 ) : 5391-5397.
  • 6Bchler T, Michalek J, Kovarova L et al. Dendritic cell-based immunotherapy for the treatment of hematological malignancies [ J ]. Hematology, 2003;8(2) :97-104.
  • 7Udono H, Srivastara P K. Heat shock protein 70-associated peptides elicits specific cancer immunity[ J]. J Exp Med, 1993 ; 178 (4) : 1391-1396.
  • 8Hayashi Y, Tohnai J, Kobayashi T et al. Trans-location of hsp-70 and protein synthesis during countinous heating at mild temperatures in Hela cells [J]. Radio Res, 1991 ; 125:80-88.
  • 9Wang X Y, Kazim L, Repasky E A et al. Characterization of heat shock protein 110 and glucose-regulated protein 170 as cancer vaccines and the effect of fever-range hyperthermia on vaccine activity [ J ]. J Immunol, 2001 ; 166(1) :490-497.
  • 10Blachere N E, Li Z, Chandawarkar R Yet al. Heat shock protein-peptide complexes,reconstituted in vitro, elicit peptide-specific cytotoxic T lymphocyte response and tumor immunity [ J ]. J Exp Med, 1997; 186 ( 8 ) : 1315-1322.

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