Literature DB >> 33738762

Molecular Mechanism of the ATF6α/S1P/S2P Signaling Pathway in Hippocampal Neuronal Apoptosis in SPS Rats.

Liang Han1,2, Yanhao Xu1, Yuxiu Shi3.   

Abstract

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.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Activating transcription factor 6α; Hippocampus; Posttraumatic stress disorder; Single prolonged stress

Mesh:

Substances:

Year:  2021        PMID: 33738762     DOI: 10.1007/s12031-021-01823-9

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  25 in total

1.  Hippocampal volume differences in Gulf War veterans with current versus lifetime posttraumatic stress disorder symptoms.

Authors:  Brigitte A Apfel; Jessica Ross; Jennifer Hlavin; Dieter J Meyerhoff; Thomas J Metzler; Charles R Marmar; Michael W Weiner; Norbert Schuff; Thomas C Neylan
Journal:  Biol Psychiatry       Date:  2010-11-20       Impact factor: 13.382

Review 2.  ER stress and the unfolded protein response in neurodegeneration.

Authors:  Claudio Hetz; Smita Saxena
Journal:  Nat Rev Neurol       Date:  2017-07-21       Impact factor: 42.937

Review 3.  A review of hippocampal activation in post-traumatic stress disorder.

Authors:  Sonalee A Joshi; Elizabeth R Duval; Bradley Kubat; Israel Liberzon
Journal:  Psychophysiology       Date:  2019-03-04       Impact factor: 4.016

4.  The value of endoplasmic reticulum stress markers (GRP78 and CHOP) in the diagnosis of acute mesenteric ischemia.

Authors:  Senol Ardic; Aysegul Gumrukcu; Ozgen Gonenc Cekic; Mehmet Erdem; Goksen Derya Reis Kose; Selim Demir; Bestami Kose; Esin Yulug; Ahmet Mentese; Suleyman Turedi
Journal:  Am J Emerg Med       Date:  2018-06-19       Impact factor: 2.469

Review 5.  Posttraumatic stress disorder post Iraq and Afghanistan: prevalence among military subgroups.

Authors:  Lindsey A Hines; Josefin Sundin; Roberto J Rona; Simon Wessely; Nicola T Fear
Journal:  Can J Psychiatry       Date:  2014-09       Impact factor: 4.356

Review 6.  Synapse impairment associated with enhanced apoptosis in post-traumatic stress disorder.

Authors:  Xinzhao Chen; Yifan Jiang; Jiayu Wang; Yishu Liu; Menglei Xiao; Congshan Song; Yu Bai; Nancy Yinuo Han; Fang Han
Journal:  Synapse       Date:  2019-09-30       Impact factor: 2.562

7.  Symptoms of posttraumatic stress disorder, depression, and anxiety among adolescents following the 2008 Wenchuan earthquake in China.

Authors:  Fang Fan; Ying Zhang; Yanyun Yang; Lei Mo; Xianchen Liu
Journal:  J Trauma Stress       Date:  2011-01-14

8.  Tacrolimus-Induced Apoptosis is Mediated by Endoplasmic Reticulum-derived Calcium-dependent Caspases-3,-12 in Jurkat Cells.

Authors:  Y W Chung; M W Chung; S K Choi; S J Choi; S J N Choi; S Y Chung
Journal:  Transplant Proc       Date:  2018-05       Impact factor: 1.066

9.  Detection of endoplasmic reticulum stress and the unfolded protein response in naturally-occurring endocrinopathic equine laminitis.

Authors:  Lynne Cassimeris; Julie B Engiles; Hannah Galantino-Homer
Journal:  BMC Vet Res       Date:  2019-01-10       Impact factor: 2.741

10.  Autophagy activated via GRP78 to alleviate endoplasmic reticulum stress for cell survival in blue light-mediated damage of A2E-laden RPEs.

Authors:  Jingyang Feng; Yuhong Chen; Bing Lu; Xiangjun Sun; Hong Zhu; Xiaodong Sun
Journal:  BMC Ophthalmol       Date:  2019-12-10       Impact factor: 2.209

View more
  1 in total

Review 1.  Neurogenic Interventions for Fear Memory via Modulation of the Hippocampal Function and Neural Circuits.

Authors:  Hee Ra Park; Mudan Cai; Eun Jin Yang
Journal:  Int J Mol Sci       Date:  2022-03-25       Impact factor: 5.923

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.