Johnson R M, King K L, Morhenn V B
Department of Cell Biology, Genentech, Inc., South San Francisco, CA 94080.
Second Messengers Phosphoproteins. 1992;14(1-2):21-37.
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.
我们研究了重组人表皮生长因子(EGF)和缓激肽(BK)刺激成人人类角质形成细胞(KC)中肌醇多磷酸和sn-1,2-二酰甘油(DAG)形成以及动员细胞内Ca2+([Ca2+]i)的能力。肌醇多磷酸通过高效液相色谱结合流动检测光谱法进行分离。使用负载fura-2的KC的数字比率成像荧光显微镜对细胞内游离钙进行定量。DAG的质量通过DAG激酶反应进行定量。当比较BK(0.1微摩尔)和EGF(200纳克/毫升)的最大剂量时,BK刺激了所测所有第二信使的更大增加。大多数细胞对BK迅速做出反应,[Ca2+]i整体增加。对EGF做出反应的细胞数量较少,反应较慢,Ca2+信号不太明显。用百日咳毒素(PTX)处理细胞24小时显著减弱了BK刺激的肌醇多磷酸形成和[Ca2+]i,而EGF反应在这两个参数上均未受影响。当培养物处理5天时,通过[3H]-胸苷掺入法测定,BK(10^-9至10^-6 M)未刺激KC中的DNA合成。这些结果表明,人KC中BK和EGF受体刺激产生的偶联和生化信号不同,提示从肌醇脂质水解刺激第二信使形成可能不是细胞增殖启动的绝对必要条件。