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转化生长因子α联结saporin对平滑肌细胞和内皮细胞具有选择性的细胞毒作用 被引量:1

Transforming growth factor-α conjugated with cytotoxin saporin inhibits specifically proliferating vascular smooth muscle cells
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摘要 目的 为证实生物导向药物TGFα SAP对增殖平滑肌细胞特异性的细胞毒性作用。方法 我们用SPDP化学联结法合成了TGFα SAP ,并用3 H TdR参入法和3 H Leucine参入法探讨了TGFα SAP对平滑肌细胞及内皮细胞的DNA合成及蛋白质合成的影响。结果 联结后的TGFα SAP对增殖平滑肌细胞的3 H TdR参入量有明显抑制作用 ,与空白对照组比较3 H TdR参入量降低了 4 4 0 % ,同时TGFα SAP亦可明显抑制平滑肌细胞的蛋白质合成 ,而saporin本身显示出的细胞毒性作用则很弱。相反 ,TGFα SAP对增殖的内皮细胞的DNA和蛋白质合成却未显示出明显的抑制作用。结论 TGFα SAP具有较saporin明显增强的细胞毒性作用 ,而与内皮细胞相比 ,TGFα AIM To testify the special cytotoxicity of TGFα SAP on proliferating vascular smooth muscle cells and endothelial cells. METHODS Conjugation of saporin to TGFα was accomplished after derivatization of saporin and TGFα with N succinimidyl 3 (2 pyridyldithio) proprionate. Cytotoxicity assays were measured by cell count. The studies of influence of TGFα SAP on values of thymidine and leucine incorporation into SMCs and ECs were measured by 3H thymidine uptake and 3H leucine uptake, respectively. RESULTS Cytotoxicity assays testified TGFα SAP conjugate could inhibit remarkably proliferation of SMCs in culture. The values of thymidine of TGFα SAP group (1×10 -9 mol·L -1 and 1×10 -7 mol·L -1 ) in comparison significantly decreased to 60 9% and 56 0% of the control group respectively, suggesting that cellular DNA synthesis obviously decreased as TGFα SAP was added. But saporin did not affect cellular DNA synthesis at higher level. The rate of 3H leucine incorporation of TGFα SAP group significantly decreased to 47 3% of the control group, suggesting that SMCs protein synthesis obviously decreased as TGFα SAP was added. But TGFα SAP at the same level did not affect DNA synthesis and protein synthesis of ECs compared with the control group. CONCLUSION TGFα SAP possesses the more effective cytotoxicity than saporin and the more specific citotoxicity on proliferating vascular smooth muscle cells than on proliferating endothelial cells.
出处 《中国药理学通报》 CAS CSCD 北大核心 2002年第2期148-152,共5页 Chinese Pharmacological Bulletin
关键词 转化生长因子Α SAPORIN 平滑肌细胞 内皮细胞 transforming growth factor α saporin vascular smooth muscle cell endothelial ce11s
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  • 1[1]Siena S, Lappi DA, Bregni M et al. Synthesis and characterization of an antihuman T-lymphocyte saporin immunotoxin (OKT1-SAP) with in vivo stability into nonhuman primates. Blood, 1988;72(2):756~65
  • 2[2]Pastore CJ, Isner JM, Bacha PA et al. Epidermal growth factor receptor-targeted cytotoxin inhibits neointimal hyperplasia in vivo. Circ Res, 1995;77(3):519~29
  • 3[3]Farb A, Lee SJ, Min DH et al. Vascular smooth muscle cell cytotoxicity and sustained inhibition of neointimal formation by fibroblast growth factor 2-saporin fusion protein. Circ Res, 1997;80(4):542~50
  • 4[4]Lin PH, Ren D, Hirko MK et al. Fibroblast growth factor-2-toxin induced cytotoxicity: differential sensitivity of co-cultured vascular smooth muscle cells and endothelial cells. Atherosclerosis, 1998;137(2):277~89
  • 5[5]Biro S, Shrivastav S, Yu ZX et al. Stimulation of endothelial cells by doses of basic-FGF-saporin are lethal to smooth muscle cells. Drug deliv: J Deliv Targeting of Therapeutic Agents,1996;3(3):155~63
  • 6[6]Chen C, Li J, Micko CJ et al. Cytotoxic effects of basic FGF and heparin binding EGF conjugated with cytotoxin saporin on vascular cell cultures. J Sur Res, 1998;75(1):35~41
  • 7[7]Blakey DC, Skilleter DN, Price RJ et al. Comparision of the pharmacokinetics and hepatotoxic effects of Saporin and ricin A-chain immu-notoxins on murine liver parenclymal cells. Carcer Res, 1988;48(24 Pt1):7072~8
  • 8[8]Epstein SE, Siegall CB, Biro S et al. Cytotoxic effects of a recombinant chimeric toxin on rapidly proliferating vascular smooth muscle cells. Circulation, 1991;84(2):778~87
  • 9[9]Pickering JG, Dov Gal, Patricia B et al. Inhibition of injury-induced intimal thickening in the rat carotid artery by a recombinant cytotoxin specific for epidermal growth factor receptor. J Am Coll Cardiol, 1991;21:178
  • 10[10]Saltis J, Thomas AC. Agrotis A et al. Expression of growth factor receptors on arterial smooth muscle cells: Dependency on cell phenotype and serum factors. Atherosclerosis, 1995;118(1):77~87

同被引文献10

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  • 2Ross R. The pathogenesis of atherosclerosis: a perspective for the 1990s[ J]. Nature, 1993,362:801 - 9.
  • 3Ross R. The smooth muscle cell. Ⅱ. Growth of smooth muscle in culture and formation of elastic fibers [ J]. J Cell Biol, 1971,50 (1):172-86.
  • 4Chamley-Campbell J,Campell G R, Ross R. Smooth musle cell in culture [ J ]. Physiol Rev, 1979 ,59 ( 1 ) : 1 - 61.
  • 5Harder D R,Sperelakis N. Action potential generation in reaggregates of rat aortic smooth muscle cells in primary culture [ J ]. Blood Vessels, 1979,16 ( 4 ) : 186 - 201.
  • 6Wakino S, Kintseher U, Kim S,et al. Retinoids inhibit proliferation of human coronary smooth muscle cells by modulating cell cycle regulators [ J ]. A rterioscler Thromb Vasc Biol, 2001,21 ( 5 ) :746 - 51.
  • 7Thyberg J, Blomgren K, Roy J, et at. Phenotypic modulation of smooth muscle cells after arterial injury is associated with changes in the distribution of laminin and fibronectiu[ J]. J Histochem Cytochem, 1997,45 (6) :837 - 46.
  • 8Newby A C. Dual role of matrix metalloproteinases (matrixins) in intimal thickening and atherosclerotic plaque rupture [ J]. Physiol Rev,2005,85( 1 ) :1 -31.
  • 9John S B. Cell separation : methods and selected applications [M ]. New York : Academic Press Inc, 1984:3.
  • 10陆卫平,王笑云,赵秀芬.膦甲酸钠干预高磷诱导的血管平滑肌细胞钙化的研究[J].中国药理学通报,2003,19(3):344-347. 被引量:1

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