Comparison of second messenger formation in human keratinocytes following stimulation with epidermal growth factor and bradykinin.

R M Johnson, K L King, V B Morhenn
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Abstract

We have examined the ability of recombinant human epidermal growth factor (EGF) and bradykinin (BK) to stimulate formation of inositol polyphosphates and sn-1,2-diacylglycerol (DAG), and mobilize intracellular Ca2+ ([Ca2+]i) in adult human keratinocytes (KC). Inositol polyphosphates were resolved by high performance liquid chromatography coupled with flow detector spectroscopy. Free intracellular calcium was quantitated using digital ratio imaging fluorescence microscopy of fura-2 loaded KC. The mass amount of DAG was quantitated using the DAG kinase reaction. When comparing maximal doses of BK (0.1 microM) and EGF (200 ng/ml), BK stimulated larger increases in all second messengers measured. The majority of cells responded rapidly to BK with global increases in [Ca2+]i. Cells responding to EGF were fewer in number and slower to respond with the Ca2+ signal being less pronounced. Treatment of cells with pertussis toxin (PTX) for 24 h significantly attenuated the BK-stimulated inositol polyphosphate formation and [Ca2+]i while the EGF response remained unaffected in both parameters. BK (10(-9) to 10(-6) M) did not stimulate DNA synthesis in KC as measured by [3H]-thymidine incorporation when cultures were treated for 5 days. These results demonstrate that the coupling and biochemical signals produced by stimulation of BK and EGF receptors in human KC are different and suggests that stimulation of second messenger formation from inositol lipid hydrolysis may not be an absolute requirement for the initiation of cell proliferation.

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表皮生长因子和缓激素刺激后人角化细胞第二信使形成的比较。
我们研究了重组人表皮生长因子(EGF)和缓激肽(BK)刺激肌醇多磷酸盐和n-1,2-二酰基甘油(DAG)形成的能力,以及在成人角质形成细胞(KC)中动员细胞内Ca2+ ([Ca2+]i)的能力。采用高效液相色谱-流动检测法对肌醇多磷酸进行了分离。用载fura-2的KC的数字比例成像荧光显微镜定量细胞内游离钙,用DAG激酶反应定量DAG的质量。当比较最大剂量BK(0.1微米)和EGF (200 ng/ml)时,BK刺激了所有测量到的第二信使的更大增加。大多数细胞对BK反应迅速,[Ca2+]i整体升高。响应EGF的细胞数量较少,响应速度较慢,Ca2+信号不太明显。百日咳毒素(PTX)处理细胞24小时显著减弱bk刺激的肌醇多磷酸形成和[Ca2+]i,而EGF反应在这两个参数中均未受到影响。BK(10(-9)至10(-6)M)在培养5天后,通过[3H]-胸腺嘧啶掺入测定,不刺激KC的DNA合成。这些结果表明,刺激BK和EGF受体在人KC中产生的偶联和生化信号是不同的,并表明刺激肌醇脂质水解形成第二信使可能不是细胞增殖起始的绝对要求。
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