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山东大学学报(医学版) ›› 2016, Vol. 54 ›› Issue (10): 11-15.doi: 10.6040/j.issn.1671-7554.0.2015.257

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Wnt3a在大鼠蛛网膜下腔出血后早期脑损伤中对神经细胞自噬和凋亡的影响

任宝鑫,马云峰,刘殿伟,李卓,姜勇   

  1. 山东大学附属济南市中心医院神经外科, 山东 济南 250012
  • 收稿日期:2015-03-10 出版日期:2016-10-10 发布日期:2016-10-10
  • 通讯作者: 姜勇. E-mail:jyong9983@aliyun.com E-mail:jyong9983@aliyun.com
  • 基金资助:
    山东省科技发展计划(2012GGA01036)

Effects of Wnt3a on neuronal autophagy and apoptosis in early brain injury after subarachnoid hemorrhage in rats

REN Baoxin, MA Yunfeng, LIU Dianwei, LI Zhuo, JIANG Yong   

  1. Department of Neurosurgery, Jinan Central Hospital Affilicated to Shandong University, Jinan 250012, Shandong, China
  • Received:2015-03-10 Online:2016-10-10 Published:2016-10-10

摘要: 目的 探讨Wnt3a在大鼠蛛网膜下腔出血(SAH)后早期脑损伤中对神经细胞自噬和凋亡的作用及影响。 方法 将75只健康雄性SD大鼠按随机数字表法分为假手术组(Sham组)、蛛网膜下腔出血组(SAH组)及干预组(Wnt3a组),每组25只;采用枕大池自体注血方法建立SAH模型,各组于出血后0、12、24、48、72 h取脑。Western bloting检测LC3Ⅱ与LC3Ⅰ的比值、Beclin-1、Caspase-3的表达情况,免疫组化染色技术观察各组大鼠海马的自噬和凋亡情况。 结果 Western bloting结果显示,SAH组LC3Ⅱ/Ⅰ、Beclin-1出血后呈升高趋势,于24 h达高峰,24 h时间点Wnt3a组LC3Ⅱ、Beclin-1的表达较SAH组明显(P<0.05)。SAH组出血后Caspase-3升高,48h达高峰,Wnt3a组Caspase-3表达较SAH组减少(P<0.05)。免疫组化结果显示,与SAH组相比,Wnt3a组24 h时间点Beclin-1阳性神经元增多,48 h时Bax阳性神经元与凋亡细胞均减少(P<0.05)。 结论 Wnt3a可以促进大鼠蛛网膜下腔出血后神经元自噬,减少神经元细胞凋亡,对神经元具有保护作用。

关键词: 蛛网膜下腔出血, Wnt3a, 凋亡, 大鼠, 自噬

Abstract: Objective To investigate the effects of Wnt3a on neuronal autophagy and apoptosis in early brain injury after subarachnoid hemorrhage(SAH)in rats. Methods A total of 75 SD male rats were randomly divided in to Sham group, SAH group and Wnt3a group. The SAH model was established by injecting autologous blood into cisterna magna. Brain was taken out after SAH at five different time points(0, 12, 24, 48, and 72 h). Western bloting was used to detect the ratio of LC3Ⅱ and LC3Ⅰ, and analyze the expressions of Beclin-1 and Caspase-3. An immunofluorescence technique was used to observe the autophagy and apoptosis of neurons. Results Western bloting results showed that in SAH group, expressions of LC3Ⅱ/Ⅰ and Beclin-1 increased after SAH and reached the peak at 24 h time point. The expressions of LC3Ⅱ and Beclin-1 in Wnt3a group were significantly higher than those in SAH group at 24 h time point(P<0.05). Caspase-3 expression, which in Wnt3a group was significantly lower than the SAH group(P<0.05), peaked at 48 h after SAH. Immunohistochemistry result showed that, compared with SAH group, the number of Beclin-1 positive neurons in Wnt3a group enhanced at 24 h while Bax positive neurons and apoptotic cells decreased at 48 h(P<0.05). Conclusion Wnt3a promotes neuronal autophagy and decreases neuronal apoptosis, which may protect the neurons.

Key words: Rats, Apoptosis, Subarachnoid hemorrhage, Wnt3a, Autophagy

中图分类号: 

  • R392.7
[1] Suzuki H, Husegawa Y, Kanamaru K, et al. Mwchanisms of osteopontin-induced stabilization of blood-brain barrier disruption after subarachnoid hemorrhage in rats[J]. Stroke, 2012, 41(8):1783-1790.
[2] Lee JY, He Y, Sagher O, et al. Activated autophagy pathway in experimental subarachnoid hemorrhage[J]. Brain Res, 2009, 1287:126-135.
[3] Matsushita K, Meng W, Wang X, et al. Evidence for apoptosis after intercerebral hemorrhage in rat striatum[J]. J Cereb Blood Flow Metab, 2000, 20(2):396-404.
[4] 黄菊芳,李岚,尚蕾,等.脑神经元死亡的研究进展[J].中国现代医学杂志,2012, 22(25):53-58. HUANG Jufang, LI Lan, SHANG Lei, et al. Research progress of brain neuron death[J]. Chinese Journal of Modern Medicine, 2012, 22(25):53-58.
[5] Shruster A, Benzur T, Melamed E, et al. Wnt signaling enhances neurogenesis and improves neurological function after focal ischemic injury.[J]. PLoS One, 2012, 7(7):398-398. doi:10.1371/jourrmal.pone. 0040843.
[6] Pan T, Kondo S, Zhu W, et al. Neuroprotection of rapamycin in lactacystin-induced neurodegeneration via autophagy enhancement[J].Neurobiol Dis, 2008, 32(1):16-25.
[7] Mizushima N. Methods for monitoring autophagy using GFP-LC3 transgenic mice[J]. Methods Enzymol, 2009, 452(12):13-23.
[8] 王嘉宁, 郭宁. 细胞凋亡的检测技术与方法[J]. 中国药理学与毒理学杂志, 2005, 19(6):466-470. WANG Jianing, GUO Ning. Techniques and methods of identifying apoptosis[J]. Chinese Journal of Pharmacology and Toxicology, 2005, 19(6):466-470.
[9] Ingall T, Asplund K, Mäh(¨overo)nen M, et al. A multinational comparison of subarachnoid hemorrhage epidemiology in the WHO MONICA stroke study [J]. Stroke, 2000, 31(5):1054-1061.
[10] Bursch W. The autophagosomal-lysosomal compartment in programmed cell death[J]. Cell Death Differ, 2001, 8(6):569-581.
[11] Uchiyama Y. Autophagic cell death and its execution by lysosomal cathepsins [J]. Arch Histol Cytol, 2001, 64(3):233-246.
[12] Kim JB, Sig Choi J, Yu YM, et al. HMGB1, a novel cytokine-like mediator linking acute neuronal death and delayed neuroinflammation in the postischemic brain[J]. J Neurosci, 2006, 26(24):6413-6421.
[13] Verkaar F, van der Doelen AA, Smits JF, et al. Inhibition of Wnt/β-catenin signaling by p38 MAP kinase inhibitors is explained by cross-reactivity with casein kinase Iδ/ε [J]. Chem Biol, 2011, 18(4):485-494.
[14] 李卓,姜惠丽,刘殿玮,等.Wnt3a在蛛网膜下腔出血后早期脑损伤中对神经发生的作用[J]. 山东大学学报(医学版), 2014, 52(5):15-19. LI Zhuo, JIANG Huili, LIU Dianwei, et al. Effects of Wnt3a on the neurogenesis in rats during early brain injury after subarachnoid hemorrhage[J]. Journal of Shandong Unversity(Health Sciences), 2014, 52(5):15-19.
[15] 张锡峰, 胡代曦, 芦永良,等. Wnt3a过表达对小鼠胚胎肝干细胞凋亡的抑制作用[J]. 细胞与分子免疫学杂志, 2014, 29(12):1277-1280. ZHANG Xifeng, HU Daixi, LU Yongliang, et al. Inhibition of Wnt3a overexpression on apoptosis of mouse embryonic liver stem cells [J]. Chinese Journal of Cellular and Molecular Immunology, 2014, 29(12):1277-1280.
[16] Shpilka T, Elazar Z. Shedding light on mammalian microautophagy.[ [J]. Developmental Dev Cell, 2011, 20(1):1-2.
[17] Edinger A L, Thompson C B. Defective autophagy leads to cancer.[ [J]. Cancer Cell, 2003, 4(6):422-424.
[18] 吕必华,张玲,刘静.COX-2抑制剂NS-398对肝癌HepG2细胞凋亡蛋白Bcl-2和Caspase-3表达的影响[J].公共卫生与预防医学, 2007, 18(4):21-24. LÜ Bihua, ZHANG Ling, LIU Jing. Expression change of apoptosis protein(Bcl-2 and Caspase-3)in HepG2 cell line induced by COX-2 inhibitor NS-398 [J]. Journal of Public Health and Preventive Medicine, 2007, 18(4):21-24.
[19] 邵云, 赵坡, 李向红. bcl-2、bax、P53在肺神经内分泌癌中表达的意义[J]. 中国肺癌杂志, 2006, 9(1):55-59. SHAO Yun, ZHAO Po, LI Xianghong. Expression and significance of bcl-2, bax, P53 in neuroendocrine carcinomas of the lung [J]. Chinese Journal of Lung Cancer, 2006, 9(1):55-59.
[20] 赵永辉,高军,李卓,等. 孕酮对蛛网膜下腔出血后早期脑损伤的保护作用[J]. 山东大学学报(医学版), 2012, 50(5):55-59. ZHAO Yonghui, GAO Jun, LI Zhuo, et al. Protective effects of progesterone on early brain injury in rats after subarachnoid hemorrhage [J]. Journal of Shandong University(Health Sciences), 2012, 50(5):55-59.
[21] 陈艾, 周晖, 童煜,等. 缺氧后胚鼠神经元自噬及凋亡相关蛋白的表达[J]. 中风与神经疾病杂志, 2012, 29(8):683-686. CHEN Ai, ZHOU Hui, TONG Yu, et al. Changes of LC3 and caspase-3 protein expression in rat fetal cortical neurons afteroxygen deprivation [J]. Journal of Apoplexy and Nervous Diseases, 2012, 29(8):683-686.
[22] Jørgensen HG, Allan EK, Jordanides NE, et al. Nilotinib exerts equipotent antiproliferative effects to imatinib and does not induce apoptosis in CD34+ CML cells[J]. Blood, 2007, 109(9):4016-4019.
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