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K^+通道在Jurkat细胞调节性体积减小中的作用 被引量:1

Effects of potassium ion channel on regulatory volume decrease in Jurkat cells
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摘要 目的 :研究K+ 通道在Jurkat细胞调节性体积减小 (RVD)中的作用。方法 :调节细胞外不同离子浓度 ,用细胞成像系统测定Jurkat细胞 (人T淋巴细胞肿瘤细胞株 )在不同渗透压时细胞容积的变化。结果 :细胞培养液中缺少Ca2 + ,或细胞培养液中的K+ 浓度升高 ,或使用Ca2 + 敏感的K+ 通道 (KCa)阻断剂均可抑制Jurkat细胞的RVD ;应激免疫抑制蛋白 (ISPS)具有抑制Jurkat细胞RVD的作用。结论 :Jurkat细胞中KCa通道是RVD不可缺少的因素。ISPS对免疫功能抑制作用的机理之一 ,可能是抑制了T淋巴细胞上的K+ AIM: To study the effect of K + channel on the regulatory volume decrease (RVD) in Jurkat cells. METHODS: An imaging analysis system was used for the measurement of cell volume under the conditions of hypotonic stress in Jurkat cells. RESULTS: RVD in Jurkat cells was found to be inhibited under the conditions of lack of Ca 2+ in the medium, and increased in concentration of K + or administration of KCa channel blocker. Immune suppressive protein of stress (ISPS) was also able to inhibit the RVD in Jurkat cells. CONCLUSION: KCa channel plays an important role in RVD in Jurkat cells. The suppression on K + channel may be one of the possible reasons for the inhibition on immune function induced by ISPS.
出处 《中国临床药理学与治疗学》 CAS CSCD 2003年第5期499-502,共4页 Chinese Journal of Clinical Pharmacology and Therapeutics
基金 国家自然科学基金项目 (№ 30 2 712 0 9)
关键词 JURKAT细胞 调节性体积减小 离子通道 免疫抑制蛋白 Jurkat cells regulatory volume decrease ion channel imunosuppressive protein
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  • 1邵黎,孙长伟,张勤,范少光,丁桂风,高珊.束缚应激能引起淋巴结及脾脏细胞产生抑制淋巴细胞转化的因子[J].科学通报,1995,40(2):164-167. 被引量:11
  • 2范少光,丁桂凤.神经内分泌与免疫系统之间相互作用的介导物质:共用的生物学语言[J].生理科学进展,1995,26(2):175-183. 被引量:100
  • 3高珊,梅林,张桂芳,范少光.束缚应激影响大鼠四氧嘧啶性糖尿病发病的初步研究[J].中国神经免疫学和神经病学杂志,1996,3(2):95-98. 被引量:4
  • 4范少光 丁桂凤.神经内分泌和免疫系统相互作用的介导物质:共用的生物学语言[J].生理科学进展,1995,26:175-183.
  • 5李一凡 左永昌 等.脑室注射白细胞介素1对淋巴细胞应激免疫抑制因子生成的影响[J].药学学报,1995,30:395-399.
  • 6Lewis RS. Calcium signaling mechanisms in T lymphocytes. Ann Rev Immunol, 2001, 19 : 497 - 521.
  • 7Guse AH, daSilva CP, Berg I, et al. Regulation of calcium signaling in T lymphocytes by the second messenger cyclic ADP-ribose. Nature, 1999, 398 : 70-73.
  • 8Hoth M. Calcium and barium permeation through calcium release-activated calcium (CRAC) channels. Pfligers Arch,1995, 430 : 315-322.
  • 9Kerschbaum HH, Cahalan MD. Single-channel recording of a store-operated Ca^2+ channel in Jurkat T lymphocytes. Science. 1999. 283 : 836 - 839.
  • 10Shieh CC, Coghlan M, James P, et al. Potassium channels:molecular defects, diseases, and therapeutic opportunities.Pharmacol Rev, 2000, 52 : 557 - 594.

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  • 1[1]Florian L, Gillian L. Busch, Markus R, Harald V, Siegfried W,et al. Functional significance of cell volume regulatory mechanisms[J]. Physiol Rev, 1998;78(1) :247-306
  • 2[3]Deutsch C, Chen LQ. Heterologous expression of specific K channels in T lymphocytes: functional consequences for volume regulation[J]. Proc Natl Acad Sci USA, 1993; 90(21): 10036-40
  • 3[4]Cahalan MD, Wulff H, Chandy KG. Molecular properties and physiological roles of ion channels in the immune system[J]. J Clin Immunol, 2001; 21(4) :235-52
  • 4[7]Jian L, Charles A. Kuszynski B. Timothy B. Doxycycline Induces Fas-Fas Ligand-Mediated Apoptosis in Jurkat T Lymphocytes[J]. Biochem Biophys Res Commun, 1999; 260(2 ): 562-7
  • 5[8]Grissrmer S, Lewis RS, Cahalan MD. Ca2+ -activated K+ channels in human leukemic T cells[J]. J Gen Physiol, 1992; 99(1) :63-84
  • 6[9]Deutsch C, Lee SC. Cell volume regulation in lymphocytes [J]. Ren Physiol Biochem, 1988; 11(3 - 5) :260-76
  • 7[10]Lewis RS, Cahalan MD. Potassium and calcium channels in lymphocytes[J]. Annu Rev Immunol, 1995; 13:623- 53
  • 8[11]Jensen BS, Odum N, Jorgensen NK, Christophersen P, Olesen SP. Inhibition of T cell proliferation by selective block of Ca2 +activated K+ channels[J]. Proc Natl Acad Sci USA, 1999;96(19): 10917-21
  • 9[12]Loria RM. Antiglucocorticoid function of androstenetriol [J].Psychoneuroendocrinology, 1997; 22(suppl 1): S103-8
  • 10徐瑶,杨解人,卞国武.六味地黄汤对氢化可的松模型小鼠的免疫调节作用[J].现代中西医结合杂志,2000,9(13):1204-1206. 被引量:16

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