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BDEO对小鼠淋巴细胞增殖和活化的影响

Effect of (E)-2-(4-bromophenyl)-1-(3,4-dihydroxyphenyl) Ethanone Oxime on Proliferation and Activation of Mice Lymphocytes

  • 摘要: 目的 观察苄基苯基酮衍生物溴苯基二羟基苯基乙酮肟(BDEO)对体外丝裂原刀豆蛋白A (Con A)刺激的小鼠脾脏淋巴细胞以及外周血液淋巴细胞增殖和活化的影响及分子机制。 方法 Con A诱导体外淋巴细胞增殖和活化,分别用细胞计数法和MTT法检测BDEO对体外淋巴细胞的转化率和增殖的影响,ELISA法测定caspase-9活性,Western blot检测Bax、Bak、Bcl-2和Cyt C(线粒体内及胞质中)以及cleaved caspase-9和cleaved caspase-3水平;进一步在整体动物水平观察腹腔注射Con A〔15 mg/(kg·d)〕和BDEO〔3、6 mg/(kg·d)〕,小鼠脾脏细胞、外周血液淋巴细胞转化率以及腹腔巨噬细胞的吞噬率。 结果 BDEO在0.3~1 μmol/L下抑制体外淋巴细胞的增殖和转化率(P<0.05),3~30 μmol/L时抑制作用逐步减弱。Caspase-9活性随BDEO浓度升高先升高后下降,而线粒体上的促凋亡蛋白Bax、Bak水平先上升后降低,而抑凋亡蛋白Bcl-2以及线粒体中Cyt C水平先降低后升高,胞质中的Cyt C、cleaved caspase-9和cleaved caspase-3水平先升高后降低。另外腹腔注射BDEO对小鼠体内的脾脏淋巴细胞和外周血液淋巴细胞的转化率以及腹腔巨噬细胞的吞噬功能具有显著抑制作用。结论 BDEO可能主要通过线粒体内源性途径,激活caspase-3通路调节淋巴细胞的增殖和活化,较低浓度时抑制淋巴细胞的增殖和活化,高浓度下抑制作用减弱。这揭示BDEO具有免疫抑制活性。

     

    Abstract: Objective To study the effects of (E)-2-(4-bromophenyl)-1-(3,4-dihydroxyphenyl) ethanone oxime (BDEO) on the proliferation and activation of the mice's splenic lymphocytes and the peripheral blood lymphocytes induced by Concanavalin A (Con A) in vitro and in vivo, and its molecular mechanism. Methods During the lymphocyte proliferation and activation induced by Con A in vitro, MTT and cell counting were used to detect the transformation rates and survival rates of lymphocytes, and ELISA was used to measure the activity of caspase-9; moreover, the levels of Bax, Bcl-2 and caspase-3 were determined by Western blot, in order to observe the effects of BDEO on cell proliferation and activation. The effects of administration of Con A 〔15 mg/(kg·d)〕 and BDEO 〔(3, 6 mg/(kg·d)〕 by intraperitoneal injection on transformation rates of spleen cells and peripheral blood lymphocyte, as well as phagocytosis rate of peritoneal macrophages in mice were also observed in vivo. Results 0.3-1 μmol/L BDEO significantly inhibited the transformation rates and growth of mice lymphocyte (P<0.05). The activity of caspase-9 and the levels of mitochondrial pro-apoptotic protein Bax and Bak gradually increased, then decreased as the BDEO continually accumulated. Anti-apoptotic protein Bcl-2 as well as mitochondrial Cyt C levels first decreased then increased gradually, and cytoplasmic Cyt C, cleaved caspase-9 and cleaved caspase-3 levels showed firstly a increase, then decrease gradually. Additionally, administration of BDEO by intraperitoneal injection significantly inhibited proliferation of spleen lymphocytes and peripheral blood lymphocyte, as well as phagocytosis of peritoneal macrophagesin in mice. Conclusion BDEO might regulate the proliferation and activation of lymphocytes through activation of caspase-3 mainly via a mitochondrial intrinsic pathway; the inhibiting CM(155mmeffect on the proliferation and transformation rate of lymphocytes was significant when the concentration of BDEO was relatively low; as the concentration accumulated increasingly, the inhibiting effect reduced. The results indicated that BDEO has immunosuppressive activity.

     

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