Yang K D, Chuen H L, Shaio M F
Department of Pediatrics, Tri-service General Hospital, Taipei, Taiwan, R.O.C.
Biochem Biophys Res Commun. 1995 Jun 26;211(3):1006-14. doi: 10.1006/bbrc.1995.1911.
We described here that pentoxifylline (PTX), which is well known to counteract tumor necrosis factor alpha (TNF alpha)-mediated inflammatory responses, augmented TNF alpha-induced neuroblastoma cell differentiation in conjunction with growth inhibition and cell-cycle arrest in G1 phase. PTX also enhanced TNF alpha-induced down-regulation of acetylcholine-mediated [Ca2+]i mobilization in neuroblastoma cells. Furthermore, we found that addition of cAMP failed to induce neuroblastoma cell differentiation, whereas blockade of [Ca2+]i mobilization by 8-(N,N-diethyl-amino)octyl-3,4,5-trimethoxybenzoate HCl (TMB-8, 10 microM) did induce neuroblastoma cell differentiation. Taken together, these results indicated that PTX possessed a novel signal transduction, down-regulation of [Ca2+]i mobilization, to augment but not counteract TNF alpha-mediated functions.
我们在此描述,己酮可可碱(PTX),众所周知可对抗肿瘤坏死因子α(TNFα)介导的炎症反应,它在抑制生长并使细胞周期停滞于G1期的同时,增强了TNFα诱导的神经母细胞瘤细胞分化。PTX还增强了TNFα诱导的神经母细胞瘤细胞中乙酰胆碱介导的[Ca2+]i动员的下调。此外,我们发现添加cAMP未能诱导神经母细胞瘤细胞分化,而用盐酸8-(N,N-二乙氨基)辛基-3,4,5-三甲氧基苯甲酸酯(TMB-8,10 microM)阻断[Ca2+]i动员确实诱导了神经母细胞瘤细胞分化。综上所述,这些结果表明PTX具有一种新的信号转导,即[Ca2+]i动员的下调,以增强而非对抗TNFα介导的功能。