NCI Office of the Director, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA.
J Mol Neurosci. 2012 Nov;48(3):660-6. doi: 10.1007/s12031-012-9785-6. Epub 2012 May 12.
The signal transduction mechanisms of pituitary adenylate cyclase activating polypeptide (PACAP) were investigated in lung cancer cells. Previously, PACAP-27 addition to NCI-H838 cells increased phosphatidylinositol turnover and intracellular cAMP leading to proliferation of lung cancer cells. Also, PACAP receptors (PAC1) regulated the tyrosine phosphorylation of ERK, focal adhesion kinase, and paxillin. In this communication, the effects of PACAP on cytosolic Ca(2+) and PYK-2 tyrosine phosphorylation were investigated. PACAP-27 increased cytosolic Ca(2+) within seconds after addition to FURA-2 AM loaded NCI-H838 cells. The increase in cytosolic Ca(2+) caused by PACAP was inhibited by PACAP(6-38) (PAC1 antagonist), U73122 (phospholipase C inhibitor), or BAPTA (calcium chelator), but not H89 (PKA inhibitor). PACAP-38, but not vasoactive intestinal peptide (VIP), addition to NCI-H838 or H1299 cells significantly increased the tyrosine phosphorylation of PYK-2 after 2 min. The increase in PYK-2 tyrosine phosphorylation caused by PACAP was inhibited by PACAP(6-38), U73122, or BAPTA, but not H89. The results suggest that PAC1 regulates PYK-2 tyrosine phosphorylation in a calcium-dependent manner.
我们研究了垂体腺苷酸环化酶激活肽(PACAP)在肺癌细胞中的信号转导机制。先前的研究表明,PACAP-27 可增加 NCI-H838 细胞中磷酸肌醇的周转率和细胞内 cAMP,从而促进肺癌细胞的增殖。此外,PACAP 受体(PAC1)调节 ERK、黏着斑激酶和桩蛋白的酪氨酸磷酸化。在本研究中,我们研究了 PACAP 对细胞质 Ca(2+)和 PYK-2 酪氨酸磷酸化的影响。PACAP-27 加入 FURA-2 AM 负载的 NCI-H838 细胞后几秒钟内即可增加细胞质 Ca(2+)。PACAP 引起的细胞质 Ca(2+)增加被 PACAP(6-38)(PAC1 拮抗剂)、U73122(PLC 抑制剂)或 BAPTA(钙螯合剂)抑制,但不被 H89(PKA 抑制剂)抑制。PACAP-38 而非血管活性肠肽(VIP)加入 NCI-H838 或 H1299 细胞后 2 分钟即可显著增加 PYK-2 的酪氨酸磷酸化。PACAP 引起的 PYK-2 酪氨酸磷酸化增加被 PACAP(6-38)、U73122 或 BAPTA 抑制,但不被 H89 抑制。这些结果表明,PAC1 通过钙依赖方式调节 PYK-2 的酪氨酸磷酸化。