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神经调节蛋白 1/表皮生长因子受体 4 诱导纹状体祖细胞迁移:钙依赖性机制和 NMDA 受体激活的调节。

Neuregulin1/ErbB4-induced migration in ST14A striatal progenitors: calcium-dependent mechanisms and modulation by NMDA receptor activation.

机构信息

Department of Animal & Human Biology, University of Turin, Via Accademia Albertina 13, Turin, Italy.

出版信息

BMC Neurosci. 2011 Oct 12;12:103. doi: 10.1186/1471-2202-12-103.

Abstract

BACKGROUND

A number of studies have separately shown that the neuregulin1 (NRG1)/ErbB4 system and NMDA-type glutamate receptors (NMDARs) are involved in several aspects of neuronal migration. In addition, intracellular calcium fluctuations play central roles in neuronal motility. Stable expression of the tyrosine kinase receptor ErbB4 promotes migratory activity in the neural progenitor cell line ST14A upon NRG1 stimulation. In this work we analyzed the potential interactions between the NRG1/ErbB4 system and NMDARs in the ST14A migratory process as well as its calcium dependence.

RESULTS

RT-PCR studies have shown that both native ST14A cells (non-expressing ErbB4), as well as ErbB4-transfected cells express low levels of a restricted number of NMDAR subunits: NR1, NR2C, NR2D and NR3B. The resulting NMDAR would form Ca(2+) channels characterized by low Mg(2+)-sensitivity and low Ca(2+)-permeability, generating small, long-lasting currents. Ca(2+)-imaging experiments showed slow Ca(2+) increases in 45% of the cells following 8 μM NMDA stimulation. Basal migration of ErbB4-transfected ST14A cells was unaffected by 18 hrs NMDA incubation. However, over the same incubation time, NMDA was able to significantly enhance NRG1-induced migration. Pre-incubation with the intracellular calcium chelator BAPTA-AM reduced both NRG1- and NRG1/NMDA-stimulated migration, suggesting the involvement of Ca(2+) in these processes. NRG1 stimulation of ErbB4-transfected ST14A cells induced a sustained, long-lasting increase in Ca(2+), in 99% of the cells. These intracellular Ca(2+) signals could be ascribed to both release from intracellular stores and influx from the extracellular medium trough a mechanism of store-operated calcium entry (SOCE). Short-time co-incubation of NMDA and NRG1 did not substantially modify the NRG1-induced intracellular calcium signals.

CONCLUSIONS

In summary, NRG1 stimulation of the ErbB4 receptor exerts a sustained Ca(2+) increase in ST14A neural progenitors; NRG1-induced migration is Ca(2+)-dependent and can be positively modulated by activation of the NMDA receptor.

摘要

背景

多项研究分别表明,神经调节蛋白 1(NRG1)/表皮生长因子受体 4(ErbB4)系统和 NMDA 型谷氨酸受体(NMDARs)参与神经元迁移的多个方面。此外,细胞内钙波动在神经元迁移中发挥核心作用。在 NRG1 刺激下,酪氨酸激酶受体 ErbB4 的稳定表达可促进神经祖细胞系 ST14A 的迁移活性。在这项工作中,我们分析了 NRG1/ErbB4 系统与 NMDAR 在 ST14A 迁移过程中的潜在相互作用及其对钙的依赖性。

结果

RT-PCR 研究表明,天然 ST14A 细胞(不表达 ErbB4)和转染 ErbB4 的细胞均表达数量有限的 NMDAR 亚基:NR1、NR2C、NR2D 和 NR3B。由此产生的 NMDAR 将形成 Ca2+通道,其特征为低 Mg2+-敏感性和低 Ca2+通透性,产生小而持久的电流。钙成像实验显示,在 8 μM NMDA 刺激后,45%的细胞中缓慢出现[Ca2+]i 增加。ErbB4 转染的 ST14A 细胞的基础迁移不受 18 小时 NMDA 孵育的影响。然而,在相同的孵育时间内,NMDA 能够显著增强 NRG1 诱导的迁移。用细胞内钙螯合剂 BAPTA-AM 预孵育可降低 NRG1 和 NRG1/NMDA 刺激的迁移,表明 Ca2+参与了这些过程。NRG1 刺激 ErbB4 转染的 ST14A 细胞诱导[Ca2+]i 持续、持久增加,99%的细胞中均出现这种情况。这些细胞内 Ca2+信号可归因于细胞内储存库的释放以及通过储存操作钙进入(SOCE)机制从细胞外介质中流入。短时间共孵育 NMDA 和 NRG1 不会显著改变 NRG1 诱导的细胞内钙信号。

结论

总之,NRG1 刺激 ErbB4 受体可使 ST14A 神经祖细胞中持续增加[Ca2+]i;NRG1 诱导的迁移依赖于 Ca2+,并可通过激活 NMDA 受体得到正向调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5061/3209446/ae2400c89db2/1471-2202-12-103-1.jpg

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