Fan Lir-Wan, Bhatt Abhay, Tien Lu-Tai, Zheng Baoying, Simpson Kimberly L, Lin Rick C S, Cai Zhengwei, Kumar Praveen, Pang Yi
Department of Pediatrics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
J Neurochem. 2015 May;133(4):532-43. doi: 10.1111/jnc.12988. Epub 2015 Jan 28.
Serotonin (5-hydroxytryptamine, 5-HT) has been implicated to play critical roles in early neural development. Recent reports have suggested that perinatal exposure to selective serotonin reuptake inhibitors (SSRIs) resulted in cortical network miswiring, abnormal social behavior, callosal myelin malformation, as well as oligodendrocyte (OL) pathology in rats. To gain further insight into the cellular and molecular mechanisms underlying SSRIs-induced OL and myelin abnormalities, we investigated the effect of 5-HT exposure on OL development, cell death, and myelination in cell culture models. First, we showed that 5-HT receptor 1A and 2A subtypes were expressed in OL lineages, using immunocytochemistry, Western blot, as well as intracellular Ca(2+) measurement. We then assessed the effect of serotonin exposure on the lineage development, expression of myelin proteins, cell death, and myelination, in purified OL and neuron-OL myelination cultures. For pure OL cultures, our results showed that 5-HT exposure led to disturbance of OL development, as indicated by aberrant process outgrowth and reduced myelin proteins expression. At higher doses, such exposure triggered a development-dependent cell death, as immature OLs exhibited increasing susceptibility to 5-HT treatment compared to OL progenitor cells (OPC). We showed further that 5-HT-induced immature OL death was mediated at least partially via 5-HT2A receptor, since cell death could be mimicked by 5-HT2A receptor agonist 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane hydrochloride, (±)-2,5-dimethoxy-4-iodoamphetamine hydrochloride, but atten-uated by pre-treatment with 5-HT2A receptor antagonist ritanserin. Utilizing a neuron-OL myelination co-culture model, our data showed that 5-HT exposure significantly reduced the number of myelinated internodes. In contrast to cell injury observed in pure OL cultures, 5-HT exposure did not lead to OL death or reduced OL density in neuron-OL co-cultures. However, abnormal patterns of contactin-associated protein (Caspr) clustering were observed at the sites of Node of Ranvier, suggesting that 5-HT exposure may affect other axon-derived factors for myelination. In summary, this is the first study to demonstrate that manipulation of serotonin levels affects OL development and myelination, which may contribute to altered neural connectivity noted in SSRIs-treated animals. The current in vitro study demonstrated that exposure to high level of serotonin (5-HT) led to aberrant oligodendrocyte (OL) development, cell injury, and myelination deficit. We propose that elevated extracellular serotonin levels in the fetal brain, such as upon the use of selective serotonin reuptake inhibitors (SSRIs) during pregnancy, may adversely affect OL development and/or myelination, thus contributing to altered neural connectivity seen in Autism Spectrum Disorders. OPC = oligodendrocyte progenitor cell.
血清素(5-羟色胺,5-HT)被认为在早期神经发育中起关键作用。最近的报告表明,围产期接触选择性5-羟色胺再摄取抑制剂(SSRIs)会导致大鼠皮质网络布线错误、异常社会行为、胼胝体髓鞘畸形以及少突胶质细胞(OL)病变。为了进一步深入了解SSRIs诱导的OL和髓鞘异常的细胞和分子机制,我们在细胞培养模型中研究了5-HT暴露对OL发育、细胞死亡和髓鞘形成的影响。首先,我们使用免疫细胞化学、蛋白质免疫印迹以及细胞内Ca(2+)测量方法,表明5-HT受体1A和2A亚型在OL谱系中表达。然后,我们评估了血清素暴露对纯化的OL和神经元-OL髓鞘形成培养物中谱系发育、髓鞘蛋白表达、细胞死亡和髓鞘形成的影响。对于纯OL培养物,我们的结果表明,5-HT暴露导致OL发育紊乱,表现为异常的突起生长和髓鞘蛋白表达减少。在较高剂量下,这种暴露引发了依赖发育的细胞死亡,因为与OL祖细胞(OPC)相比,未成熟的OL对5-HT处理表现出更高的敏感性。我们进一步表明,5-HT诱导的未成熟OL死亡至少部分是通过5-HT2A受体介导的,因为细胞死亡可以被5-HT2A受体激动剂1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷盐酸盐,(±)-2,5-二甲氧基-4-碘苯丙胺盐酸盐模拟,但可通过用5-HT2A受体拮抗剂利坦色林预处理来减轻。利用神经元-OL髓鞘形成共培养模型,我们的数据表明,5-HT暴露显著减少了有髓神经节间段的数量。与在纯OL培养物中观察到的细胞损伤相反,5-HT暴露在神经元-OL共培养物中不会导致OL死亡或OL密度降低。然而,在郎飞结部位观察到接触蛋白相关蛋白(Caspr)聚集的异常模式,这表明5-HT暴露可能会影响其他轴突衍生的髓鞘形成因子。总之,这是第一项证明操纵血清素水平会影响OL发育和髓鞘形成的研究,这可能导致在接受SSRIs治疗的动物中观察到的神经连接改变。目前的体外研究表明,暴露于高水平的血清素(5-HT)会导致少突胶质细胞(OL)发育异常、细胞损伤和髓鞘形成缺陷。我们认为,胎儿大脑中细胞外血清素水平升高,例如在怀孕期间使用选择性5-羟色胺再摄取抑制剂(SSRIs)时,可能会对OL发育和/或髓鞘形成产生不利影响,从而导致自闭症谱系障碍中出现的神经连接改变。OPC = 少突胶质细胞祖细胞