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醋酸锌对大鼠胚胎肢芽细胞增殖和分化影响的研究 被引量:1

Effect of Zinc Acetate on Proliferation and differentiation of Rat Embryonic Limb Bud Cell
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摘要 目的 研究醋酸锌对原代培养的大鼠胚胎肢芽细胞形态、细胞相对蛋白含量、细胞集落形成率以及肢芽细胞生长发育的影响。方法 取SD大鼠胚胎肢芽组织,分别加入不同浓度的醋酸锌进行体外原代微团培养。用光学显微镜观察细胞形态,在倒置相差显微镜下计数细胞集落数,同时用Folin-酚法检测细胞蛋白含量。结果 当锌浓度为0.05mmol/L时,对肢芽细胞生长和集落的形成无显著影响,而当锌浓度增至0.1mmol/L时,表现出显著促进作用,锌浓度大于1.0mmol/L时则呈现抑制作用,且影响的程度随着锌浓度的增加而增强。醋酸锌对大鼠胚胎肢芽细胞的半数分化抑制浓度(ICD50)为1360.9μg/mL。结论 醋酸锌对胚胎肢芽细胞增殖和分化的影响呈现双向效应,即低浓度促进,高浓度抑制。 Objective: To study the effect of zinc on embryo, the growth of limb bud cell was observed in vitro by counting the number of colony in culture and detecting the level of cellular protein. Methods: Embryonic cells from 14-day SD rats were primarily cultured in 96 well plate with different concentrations of zinc acetate. Amount of cellular colony was counted under phase-contrast microscope, the level of cellular protein was detected using Folin-phenol method and the cell-morphology was observed with microscope. Results: 0.1mmol/L of zinc promoted the proliferation of limb bud cells and the colony forming, But more than 1.0mmol/L of zinc showed the inhibiting effect. The concentration of zinc to inhibit the formation of differentiation foci by 50% of the control (ICD 50) was shown to be 1360.9μg/mL. Conclusion: The condign dose of zinc can promote the growth of limb bud cell, but over-dose of zinc displayed an inhibited effect.
出处 《河南预防医学杂志》 2005年第2期70-72,共3页 Henan Journal of Preventive Medicine
关键词 醋酸锌 胚胎肢芽细胞 原代培养 Zinc acetate Embryonic limb bud cell Primary culture
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参考文献10

  • 1侯永根,端礼荣,吴全义,邢光伟.氯化锂对大鼠胚胎中脑神经细胞毒性作用的研究[J].江苏大学学报(医学版),2003,13(4):323-324. 被引量:2
  • 2端礼荣,刘静,王苏华,刘丽群.锌对大鼠胚胎脑神经元细胞生长发育作用研究[J].中国公共卫生,2002,18(3):271-272. 被引量:5
  • 3陈婉蓉,傅中滇.应用神经细胞微团培养法筛选化学致畸物[J].中华预防医学杂志,1991,25(3):180-182. 被引量:19
  • 4Slomianka L. Neuros of origin of zinc containing pathways and the distribution of zinc containing boutons in the hippocampal region of the rat[J]. Neuroscience, 1992,48:325.
  • 5Leonard A, Hantson PH,Gerber GB,et al., Mutagenicity,carcinogenicity and tertogenicity of lithium compounds. Mur Res,1995,339:131-137.
  • 6Flint OP.An in vitro test for teratens:Desirable and points,test batteries, and current status of the micromass teratogen test. Reprodue Toxicol, 1993,7:103-111.
  • 7Zhang X, Ziraw N, Goater JJ, et al., Primary murine limb bud mesenchymal cells in long-term culture complete chondrocyte differentiation TGF-beta delays hypertrophy and PGE2 inhibits terminal differentiation. Bone, 2004, 34:809-817.
  • 8Saillenfait AM, Sabate JP & Gaspard C, Effects of aliphatic nitriles in micromass cultures of rat embryo limb bud cells. Toxicol In Vitro,2004, 18:311-318.
  • 9Wang B, Ohyama H, Shang Y, et al., Adaptive response in embryogenesis: IV. Protective and detrimental bystander effects induced by X radiation in cultured limb bud cells of fetal mice. Radiat Res, 2004, 161:9-16.
  • 10Huang C & Hales BF, Role of caspases in murine limb bud cell death induced by 4-hydroperoxy cyclophosphamide, an activated analog of cyclophosphamide. Teratology, 2002; 66(6):288-299.

二级参考文献11

  • 1Sher.,AR,韩维栋.锌,铜和铁元素的营养和免疫[J].国外医学(医学地理分册),1993,14(1):14-15. 被引量:4
  • 2盛晓阳,洪昭毅,章依文,周建德.锌对幼鼠脑发育的影响[J].营养学报,1994,16(2):115-120. 被引量:19
  • 3Leonard A, Hantson PH, Gerber GB. Mutagenieity, carcinogenicity and tertogenicity of lithium compounds [ J ].Mut Res, 1995,339:131.
  • 4Flint OP. An in vitro test for teratens: Desirable and points, test batteries , and eurrent status of the micromass teratogen test[J]. Reprodue Toxicol, 1993, 7 :103.
  • 5Ribeiro PL. Chemieally induced growth inhibition and cell cycle perturbations in cultures of differentiating rodent embryrmie cells[J]. Toxieol Appl Pharmacol, 1990,104:200.
  • 6Sobit RC, Sharma M, Gill RK. Frequency of sisters chromatid exchanges(SCEs) and chromosome aberration(CAS) caused by three salts of lithium(in vitro)[J].Cytologia, 1989,45:245.
  • 7陈婉蓉,环境与健康杂志,1988年,29卷,5页
  • 8傅中滇,卫生毒理学杂志,1988年,2卷,224页
  • 9傅中滇,中华预防医学杂志,1986年,20卷,369页
  • 10陈婉蓉,傅中滇.应用神经细胞微团培养法筛选化学致畸物[J].中华预防医学杂志,1991,25(3):180-182. 被引量:19

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