Lelievre Vincent, Hu Zhongting, Byun Ji-Yun, Ioffe Yevgeniya, Waschek James A
Department of Psychiatry and Mental Retardation Research Center, Neuropsychiatric Institute, University of California at Los Angeles, Los Angeles, California 90024, USA.
J Neurosci Res. 2002 Mar 1;67(5):566-73. doi: 10.1002/jnr.10153.
Pituitary adenylyl cyclase activating peptide (PACAP) has been shown either to stimulate or to inhibit neural cell proliferation depending on the origin of the cell population. We show here that, depending on the presence or absence of fibroblast growth factor-2 (FGF-2, also called basic FGF), PACAP may either stimulate or inhibit DNA synthesis in neural precursors isolated from embryonic day 10.5 mouse hindbrain. In the absence of FGF-2, PACAP stimulated 3H-thymidine incorporation in a dose-dependent manner. This stimulatory action was unaffected by antagonists of protein kinases A and C but was abolished in the presence of the MEK1/2 antagonist PD98059. In contrast, when FGF-2 was present, PACAP inhibited DNA synthesis. This inhibitory action was insensitive to PD98059 but was fully blocked by the protein kinase A (PKA) inhibitor H89. The differential blockades by MEK1/2 and PKA inhibitors indicate that the FGF-2-induced switch in PACAP action on DNA synthesis was accomplished by a change in PACAP signaling pathways. We hypothesize that the actions of PACAP in the specific parts of the developing nervous system are determined in part by the presence or absence of FGFs and other growth factors.
垂体腺苷酸环化酶激活肽(PACAP)已被证明根据细胞群体的来源,既能刺激也能抑制神经细胞增殖。我们在此表明,根据成纤维细胞生长因子2(FGF-2,也称为碱性FGF)的存在与否,PACAP可能刺激或抑制从胚胎第10.5天小鼠后脑分离的神经前体细胞中的DNA合成。在没有FGF-2的情况下,PACAP以剂量依赖的方式刺激3H-胸腺嘧啶核苷掺入。这种刺激作用不受蛋白激酶A和C拮抗剂的影响,但在存在MEK1/2拮抗剂PD98059时被消除。相反,当存在FGF-2时,PACAP抑制DNA合成。这种抑制作用对PD98059不敏感,但被蛋白激酶A(PKA)抑制剂H89完全阻断。MEK1/2和PKA抑制剂的不同阻断表明,FGF-2诱导的PACAP对DNA合成作用的转换是通过PACAP信号通路的改变实现的。我们推测,PACAP在发育中的神经系统特定部位的作用部分由FGFs和其他生长因子的存在与否决定。