Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China.
Department of Neurology, University of Massachusetts Medical School, Worcester, MA 01604, USA.
Int J Mol Med. 2018 Jun;41(6):3457-3467. doi: 10.3892/ijmm.2018.3543. Epub 2018 Mar 7.
Ephrin‑B3 is important in the regulation of cell proliferation, differentiation and migration via cell‑cell contact, and can activate the reelin pathway during brain development. However, the effect of ephrin‑B3 on hippocampal neurogenesis and the reelin pathway in epilepsy remains to be fully elucidated. In the present study, the expression of ephrin‑B3 in pilocarpine‑induced status epilepticus (SE) rats was investigated. SYBR Green‑based reverse transcription‑quantitative polymerase chain reaction analysis, immunohistochemical labeling and western blot analysis were used to detect the gene and protein expression levels of ephrin‑B3 and reelin pathway proteins. Immunofluorescence staining of doublecortin (DCX) was utilized to analyze hippocampal neurogenesis. The data revealed that the mRNA and protein expression levels of ephrin‑B3 in the hippocampus decreased during the spontaneous seizure period. Of note, the expression of reelin and its downstream phosphorylation disabled 1 (p‑Dab1) were also notably decreased during the spontaneous seizure period, which showed similar dynamic changes as in the expression of ephrin‑B3. In addition, it was found that the number of DCX‑labeled neuronal progenitor cells was increased in the hippocampus following pilocarpine‑induced SE. To further clarify the role of ephrin‑B3 in neurogenesis and the reelin pathway in epilepsy, an exogenous ephrin‑B3 clustering stimulator, EphB3‑Fc, was infused into the bilateral hippocampus of the rats post‑SE. Following EphB3‑Fc injection, it was found that the expression levels of reelin and p‑Dab1 were significantly increased in the epileptic rats following EphB3‑Fc injection. The number of DCX‑labeled neuronal progenitor cells was reduced in the hippocampus of the epileptic rats. Furthermore, the intensity and frequency of spontaneous recurrent seizures and electroencephalographic seizures were attenuated in the epileptic rats post‑injection. These results demonstrated the critical role of ephrin‑B3 in regulation of the reelin pathway and hippocampal neurogenesis in epilepsy, providing experimental evidence that ephrin‑B3 functions as a potential protective factor in epilepsy, at least in animals.
Ephrin-B3 通过细胞间接触在细胞增殖、分化和迁移的调节中起重要作用,并在大脑发育过程中激活 reelin 途径。然而,ephrin-B3 对癫痫中海马神经发生和 reelin 途径的影响仍有待充分阐明。在本研究中,研究了 Ephrin-B3 在匹罗卡品诱导的癫痫持续状态(SE)大鼠中的表达。采用 SYBR Green 逆转录定量聚合酶链反应分析、免疫组织化学标记和 Western blot 分析检测 Ephrin-B3 和 reelin 途径蛋白的基因和蛋白表达水平。采用双皮质素(DCX)免疫荧光染色分析海马神经发生。结果显示,在自发性发作期间,海马 Ephrin-B3 的 mRNA 和蛋白表达水平降低。值得注意的是,reelin 及其下游磷酸化的 disabled 1(p-Dab1)的表达在自发性发作期间也显著降低,与 Ephrin-B3 的表达呈现相似的动态变化。此外,发现匹罗卡品诱导 SE 后海马中 DCX 标记的神经祖细胞数量增加。为了进一步阐明 Ephrin-B3 在神经发生和癫痫中的 reelin 途径中的作用,在 SE 后将 Ephrin-B3 聚类刺激物 EphB3-Fc 注入大鼠双侧海马。EphB3-Fc 注射后,发现 EphB3-Fc 注射后癫痫大鼠 reelin 和 p-Dab1 的表达水平显著升高。癫痫大鼠海马中 DCX 标记的神经祖细胞数量减少。此外,EphB3-Fc 注射后癫痫大鼠的自发性复发发作强度和频率以及脑电图发作均减轻。这些结果表明 Ephrin-B3 在癫痫中调节 reelin 途径和海马神经发生中起关键作用,为 Ephrin-B3 在癫痫中作为潜在保护因子的作用提供了实验证据,至少在动物中如此。