Hoffman J R, Boyne L J, Levitt P, Fischer I
Department of Biology, Beaver College, Glenside, PA 19038, USA.
J Neurosci Res. 1996 Nov 1;46(3):349-59. doi: 10.1002/(SICI)1097-4547(19961101)46:3<349::AID-JNR8>3.0.CO;2-K.
Methylazoxymethanol (MAM) is an alkylating agent that is used to induce microencephaly by killing mitotically active neuroblasts. We found that at later developmental times, MAM exposure can result in abnormal fiber growth in vivo. However, there have not been any previous studies on the effects of MAM on differentiating neurons. We examined the outcome of short exposure to MAM on postmitotic embryonic hippocampal cultures during the establishment of axonal polarity. At 0, 1, or 2 days in vitro (DIV), neurons were treated with 0.1 nM-1 microM MAM for 3 hr and then transferred to glial conditioned media. At 3 DIV, the cells were fixed and analyzed by immunofluorescent staining for neuron viability and differentiation. Control cells initiate several minor processes; one process elongates rapidly at about 1 DIV eventually becoming an axon, while extensive dendritic growth occurs after 3-4 DIV. Neurons treated with 1 microM MAM at 0 or 1 DIV showed a marked inhibition of neurite growth and withdrawal of axons without affecting cell viability. These cells continued to show minimal neurite outgrowth at 7 DIV, even when transferred to a glial coculture. In contrast, cells treated initially with MAM, after neuronal polarity is established at 2 DIV, showed no effect on axonal growth. To determine the effects of MAM on the neuronal cytoskeleton, we examined the in vitro assembly of brain microtubules in a one cycle assay. Exposure to MAM depleted the soluble pool of proteins, including microtubule-associated protein 1B (MAP1B) and MAP2, which are required for neurite outgrowth, through a nonspecific process. Under non-saturating conditions, there were no changes in the total amount of microtubules assembled or the coassembly of MAP1B and MAP2 in the presence of MAM. These results demonstrate that MAM can directly affect differentiating neurons, indicating that an early disruption of axonal outgrowth may have long-term effects.
甲基偶氮甲醇(MAM)是一种烷基化剂,通过杀死有丝分裂活跃的神经母细胞来诱导小头畸形。我们发现,在发育后期,暴露于MAM会导致体内纤维生长异常。然而,之前尚无关于MAM对分化神经元影响的研究。我们研究了在轴突极性建立过程中,短期暴露于MAM对有丝分裂后胚胎海马培养物的影响。在体外培养的第0、1或2天(DIV),用0.1 nM - 1 μM的MAM处理神经元3小时,然后转移到胶质细胞条件培养基中。在第3 DIV时,固定细胞并通过免疫荧光染色分析神经元活力和分化情况。对照细胞开始形成几个小的突起;一个突起在大约1 DIV时迅速伸长,最终成为轴突,而广泛的树突生长在3 - 4 DIV后发生。在0或1 DIV时用1 μM MAM处理的神经元显示出神经突生长明显受到抑制,轴突回缩,且不影响细胞活力。即使转移到胶质细胞共培养中,这些细胞在7 DIV时仍显示出最小程度的神经突生长。相比之下,如果在2 DIV神经元极性建立后最初用MAM处理细胞,则对轴突生长没有影响。为了确定MAM对神经元细胞骨架的影响,我们在一个循环试验中检查了脑微管的体外组装。暴露于MAM通过一个非特异性过程耗尽了包括神经突生长所需的微管相关蛋白1B(MAP1B)和MAP2在内的可溶性蛋白池。在非饱和条件下,在存在MAM的情况下,组装的微管总量或MAP1B和MAP2的共组装没有变化。这些结果表明,MAM可以直接影响分化中的神经元,表明轴突生长的早期破坏可能具有长期影响。