PTSD Laboratory, Department of Histology and Embryology, School of Basic Medicine, China Medical University, Shenyang, China.
Department of Thoracic Surgery, Third Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
J Mol Neurosci. 2021 Dec;71(12):2487-2499. doi: 10.1007/s12031-021-01823-9. Epub 2021 Mar 18.
Apoptosis of hippocampal neurons is one of the mechanisms of hippocampal atrophy in posttraumatic stress disorder (PTSD), and it is also an important cause of memory impairment in PTSD patients. Endoplasmic reticulum stress (ERS) mediated by activated transcription factor 6α (ATF6α)/site 1 protease (S1P)/S2P is involved in cell apoptosis, but it is not clear whether it is involved in hippocampal neuron apoptosis caused by PTSD. A PTSD rat model was constructed by the single prolonged stress (SPS) method. The study was divided into three parts. Experiment 1 included the control group, SPS 1 d group, SPS 7 d group, and SPS 14 d group. Experiment 2 included the control group, SPS 7 d group, SPS 7 d + AEBSF group, and control + AEBSF group. (4-(2-Aminoethyl)benzenesulfonyl fluoride hydrochloride (AEBSF) is an ATF6α pathway inhibitor). Experiment 3 included the control group, SPS 4 d group, SPS 4 d + AEBSF group, and control + AEBSF group. The protein and mRNA expression levels of ATF6α, glucose-regulated protein (GRP78), S1P, S2P, C/EBP homologous protein (CHOP), and caspase-12 in the hippocampus of PTSD rats were detected by immunohistochemistry, Western blotting and qRT-PCR. Apoptosis of hippocampal neurons was detected by TUNEL staining. In experiment 1, the protein and mRNA expression of ATF6α and GRP78 increased gradually in the SPS 1 d group and the SPS 7 d group but decreased in the SPS 14 d group (P < 0.01). In experiment 2, compared with that in the control group, the protein and mRNA expression of ATF6α, GRP78, S1P, S2P, CHOP, and caspase-12 and the apoptosis rate were significantly increased in the SPS 7 d group (P < 0.01). However, the protein and mRNA expression of ATF6α, GRP78, S1P, S2P, CHOP, and caspase-12 and the apoptosis rate were significantly decreased after AEBSF pretreatment (P < 0.01). In experiment 3, compared with that in the control group, the protein and mRNA expression of ATF6α, GRP78, S1P, S2P, CHOP, and caspase-12 and the apoptosis rate were increased in the SPS 14 d group (P < 0.05). However, the protein and mRNA expression of ATF6α, GRP78, S1P, S2P, CHOP, and caspase-12 and the apoptosis rate were decreased after AEBSF pretreatment (P < 0.05). SPS induced apoptosis of hippocampal neurons by activating ERS mediated by ATF6α, suggesting that ERS-induced apoptosis is involved in the occurrence of PTSD.
海马神经元凋亡是创伤后应激障碍 (PTSD) 中海马萎缩的机制之一,也是 PTSD 患者记忆障碍的重要原因。激活的转录因子 6α (ATF6α)/位点 1 蛋白酶 (S1P)/S2P 介导的内质网应激 (ERS) 参与细胞凋亡,但尚不清楚其是否参与 PTSD 引起的海马神经元凋亡。通过单次延长应激 (SPS) 方法构建 PTSD 大鼠模型。该研究分为三个部分。实验 1 包括对照组、SPS 1 d 组、SPS 7 d 组和 SPS 14 d 组。实验 2 包括对照组、SPS 7 d 组、SPS 7 d+AEBSF 组和对照组+AEBSF 组。(4-(2-氨乙基)苯磺酰氟盐酸盐 (AEBSF) 是 ATF6α 途径抑制剂)。实验 3 包括对照组、SPS 4 d 组、SPS 4 d+AEBSF 组和对照组+AEBSF 组。通过免疫组织化学、Western blot 和 qRT-PCR 检测 PTSD 大鼠海马中 ATF6α、葡萄糖调节蛋白 (GRP78)、S1P、S2P、C/EBP 同源蛋白 (CHOP) 和半胱天冬酶-12 的蛋白和 mRNA 表达水平。通过 TUNEL 染色检测海马神经元凋亡。在实验 1 中,SPS 1 d 组和 SPS 7 d 组 ATF6α 和 GRP78 的蛋白和 mRNA 表达逐渐增加,但 SPS 14 d 组减少(P<0.01)。在实验 2 中,与对照组相比,SPS 7 d 组 ATF6α、GRP78、S1P、S2P、CHOP 和半胱天冬酶-12 的蛋白和 mRNA 表达以及细胞凋亡率明显增加(P<0.01)。然而,AEBSF 预处理后,ATF6α、GRP78、S1P、S2P、CHOP 和半胱天冬酶-12 的蛋白和 mRNA 表达以及细胞凋亡率明显降低(P<0.01)。在实验 3 中,与对照组相比,SPS 14 d 组 ATF6α、GRP78、S1P、S2P、CHOP 和半胱天冬酶-12 的蛋白和 mRNA 表达以及细胞凋亡率增加(P<0.05)。然而,AEBSF 预处理后,ATF6α、GRP78、S1P、S2P、CHOP 和半胱天冬酶-12 的蛋白和 mRNA 表达以及细胞凋亡率降低(P<0.05)。SPS 通过激活 ATF6α 介导的 ERS 诱导海马神经元凋亡,提示 ERS 诱导的凋亡参与 PTSD 的发生。