J R Nofer, E Pulawski, R Junker, U Seedorf, G Assmann, W Zidek, M Tepel
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引用次数: 6
摘要
Thapsigargin已被证明可提高人淋巴细胞内Na(+)浓度,但其诱导Na(+)进入的机制尚不清楚。在本研究中,我们研究了thapsigargin与两种结构无关的化合物二甲硫脲和bepridil抑制Na(+)/Ca(2+)交换后,诱导的人淋巴细胞胞浆游离Na(+)和Ca(2+)浓度的变化。5 μ m thapsigargin诱导的细胞内Na(+)增加在5 μ m二甲基硫脲或40 μ m bepridil存在下显著增强。相比之下,这两种化合物都显著降低了thapsigargin诱导的细胞内Ca(2+)升高。在没有细胞外Na(+)的情况下,没有观察到二甲硫脲或贝必地尔对萨普格素诱导的Ca(2+)内流的影响。这些观察结果与thapsigargin刺激人淋巴细胞Na(+)/Ca(2+)交换的假设一致。然而,Na(+)/Ca(2+)交换并不介导Na(+)在人淋巴细胞内的内流。
Na(+)/Ca(2+) exchange inhibitors modulate thapsigargin-induced Ca(2+) and Na(+) influx in human lymphocytes.
Thapsigargin has been shown the elevate intracellular Na(+) concentration in human lymphocytes, but mechanisms underlying thapsigargin-induced Na(+) entry are little understood. In the present study we investigated thapsigargin-induced changes in cytosolic free Na(+) and Ca(2+) concentration in human lymphocytes after inhibition of the Na(+)/Ca(2+) exchange with two structurally unrelated compounds, dimethylthiourea ad bepridil. The intracellular Na(+) increase induced by 5 microM thapsigargin was significantly enhanced in the presence of 5 mM dimethylthiourea or 40 microM bepridil. In contrast, both compounds significantly decreased the thapsigargin-induced intracellular Ca(2+) elevation. No effect of dimethylthiourea or bepridil on thapsigargin-induced Ca(2+) influx was observed in the absence of extracellular Na(+). These observations are consistent with the hypothesis that thapsigargin stimulates Na(+)/Ca(2+ )exchange in human lymphocytes. However, Na(+)/Ca(2+) exchange does not mediate Na(+) influx in human lymphocytes.