机构:[1]Air Force Mil Med Univ, Xijing Hosp, Dept Anesthesiol & Perioperat Med, Xian 710032, Peoples R China[2]Capital Med Univ, Beijing Tongren Hosp, Dept Anesthesiol, Beijing 100730, Peoples R China临床科室麻醉科首都医科大学附属北京同仁医院首都医科大学附属同仁医院[3]Chinese Peoples Liberat Army Gen Hosp, Dept Anesthesiol, Med Ctr 1, Beijing 100853, Peoples R China[4]Chinese Peoples Liberat Army Gen Hosp, Dept Burn & Plast Surg, Med Ctr 4, Beijing 100048, Peoples R China[5]Nantong Univ, Dept Anesthesiol, Affiliated Hosp, Nantong 226001, Peoples R China[6]Chinese Peoples Liberat Army Gen Hosp, Dept Anesthesiol, Med Ctr 7, Beijing 100700, Peoples R China[7]Chinese Peoples Liberat Army Gen Hosp, Dept Pulm & Crit Care Med, Beijing, Peoples R China
Growing evidence indicates that estrogen plays a pivotal role in neuroprotection against cerebral ischemia, but the molecular mechanism of this protection is still elusive. N-myc downstream-regulated gene 2 (Ndrg2), an estrogen-targeted gene, has been shown to exert neuroprotective effects against cerebral ischemia in male mice. However, the role of Ndrg2 in the neuroprotective effect of estrogen remains unknown. In this study, we first detected NDRG2 expression levels in the cortex and striatum in both female and male mice with western blot analyses. We then detected cerebral ischemic injury by constructing middle cerebral artery occlusion and reperfusion (MCAO-R) models in Ndrg2 knockout or conditional knockdown female mice. We further implemented estrogen, ER alpha, or ER beta agonist replacement in the ovariectomized (OVX) Ndrg2 knockout or conditional knockdown female mice, then tested for NDRG2 expression, glial fibrillary acidic protein (GFAP) expression, and extent of cerebral ischemic injury. We found that NDRG2 expression was significantly higher in female than in male mice in both the cortex and striatum. Ndrg2 knockouts and conditional knockdowns showed significantly aggravated cerebral ischemic injury in female mice. Estrogen and ER beta replacement treatment (DPN) led to NDRG2 upregulation in both the cortex and striatum of OVX mice. Estrogen and DPN also led to GFAP upregulation in OVX mice. However, the effect of estrogen and DPN in activating astrocytes was lost in Ndrg2 knockout OVX mice and primary cultured astrocytes, but partially retained in conditional knockdown OVX mice. Most importantly, we found that the neuroprotective effects of E2 and DPN against cerebral ischemic injury were lost in Ndrg2 knockout OVX mice but partially retained in conditional knockdown OVX mice. These findings demonstrate that estrogen alleviated cerebral ischemic injury via ER beta upregulation of Ndrg2, which could activate astrocytes, indicating that Ndrg2 is a critical mediator of E2-induced neuroprotection against cerebral ischemic injury.
基金:
National Natural Science
Foundation of China (no. 81801138, 81971226, 82003321, 82171464,
82101427, 81901097), Science Key Program of Military Logistics
(BLB20J002), National Key Research and Development Program of
China (no. 2018YFC2001905).
第一作者机构:[1]Air Force Mil Med Univ, Xijing Hosp, Dept Anesthesiol & Perioperat Med, Xian 710032, Peoples R China
共同第一作者:
通讯作者:
推荐引用方式(GB/T 7714):
Wang Jin,Liu Min,Hou Wugang,et al.N-myc Downstream-Regulated Gene 2 (Ndrg2): A Critical Mediator of Estrogen-Induced Neuroprotection Against Cerebral Ischemic Injury[J].MOLECULAR NEUROBIOLOGY.2022,59(8):4793-4804.doi:10.1007/s12035-022-02877-5.
APA:
Wang, Jin,Liu, Min,Hou, Wugang,Hou, Min,Zhang, Lixia...&Ma, Yulong.(2022).N-myc Downstream-Regulated Gene 2 (Ndrg2): A Critical Mediator of Estrogen-Induced Neuroprotection Against Cerebral Ischemic Injury.MOLECULAR NEUROBIOLOGY,59,(8)
MLA:
Wang, Jin,et al."N-myc Downstream-Regulated Gene 2 (Ndrg2): A Critical Mediator of Estrogen-Induced Neuroprotection Against Cerebral Ischemic Injury".MOLECULAR NEUROBIOLOGY 59..8(2022):4793-4804