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400042 重庆,陆军军医大学(第三军医大学)第三附属医院(野战外科研究所)神经内科
[ 许志强,E-mail: xzq881@163.com XU Zhiqiang, E-mail: xzq881@163.com
收稿:2018-08-12,
修回:2018-10-16,
纸质出版:2019-01-30
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许曼玉, 陈甲, 许志强. AAV-proBDNF对阿尔茨海默病鼠海马DCX阳性细胞数及PSD-95表达的影响[J]. 第三军医大学学报, 2019,41(2):95-99.
Manyu XU, Jia CHEN, Zhiqiang XU. Effects of AAV-proBDNF on hippocampal DCX positive cells and PSD-95 expression in Alzheimer's disease mice[J]. Journal of Third Military Medical University, 2019, 41(2): 95-99.
许曼玉, 陈甲, 许志强. AAV-proBDNF对阿尔茨海默病鼠海马DCX阳性细胞数及PSD-95表达的影响[J]. 第三军医大学学报, 2019,41(2):95-99. DOI: 10.16016/j.1000-5404.201808088.
Manyu XU, Jia CHEN, Zhiqiang XU. Effects of AAV-proBDNF on hippocampal DCX positive cells and PSD-95 expression in Alzheimer's disease mice[J]. Journal of Third Military Medical University, 2019, 41(2): 95-99. DOI: 10.16016/j.1000-5404.201808088.
目的
2
探讨侧脑室注射携带抗裂解脑源性神经营养因子前体(proBDNF)基因的腺相关病毒基因整合载体(AAV-proBDNF)对阿尔茨海默病小鼠(AD鼠)海马神经形成与生长的影响。
方法
2
取5月龄APP/PS1转基因AD鼠15只,采用抛硬币法随机分为正常对照组(
n
=5)、空载体对照组(
n
=5)和AAV-proBDNF组(
n
=5),AAV-proBDNF组右侧侧脑室注射AAV-proBDNF(4 μL
2×10
13
v.g./mL),空载体对照组右侧侧脑室注射等量空病毒载体,正常对照组右侧侧脑室注射生理盐水(4 μL)。于侧脑室注射后4周采用ELISA检测海马proBDNF含量,免疫组化检测海马齿状回DCX阳性细胞数,Western blot检测海马突触后致密物-95(PSD-95)表达。
结果
2
侧脑室注射后4周,AAV-proBDNF组脑内proBDNF表达水平较正常对照组明显增加,且显著高于空载体对照组,差异均具有统计学意义(
P
<
0.05);AAV-proBDNF组海马DCX阳性细胞数为(202.46±24.27),明显低于正常对照组(382.26±37.58,
P
<
0.05)和空载体对照组(365.48±32.68,
P
<
0.05);AAV-proBDNF组海马PSD-95相对含量为(0.62±0.05),明显低于正常对照组(0.82±0.02,
P
<
0.05)和空载体对照组(0.86±0.07,
P
<
0.05)。
结论
2
侧脑室注射AAV-proBDNF能够在AD鼠脑内成功表达proBDNF,并可降低AD鼠海马区新生神经元数量及突触可塑性。
Objective
2
To explore the effects of lateral ventricle injection of recombinant adeno-associated virus-brain-derived neurotrophic factor precursor (AAV-proBDNF) on the hippocampal neurogenesis in APPswePS1dE9 transgenic mice (Alzheimer's disease
AD).
Methods
2
Fifteen APP/PS1 dE9 transgenic mice (5 months old) were randomly divided into normal control
empty vector control and AAV-proBDNF groups (
n
=5 in each group). Recombinant vectors of AAV-proBDNF (8×10
10
v.g.) were stereotaxically delivered into the right lateral ventricle in the AAV-proBDNF group
and empty AAV vector and normal saline (4 μL) were given respectively to the mice from the empty vector control and normal control groups. Enzyme-linked imm
unosorbent assay was conducted to test the proBDNF level in the brain in 4 weeks after injection. The count of doublecortin (DCX) positive cells and the expression of postsynaptic density-95 (PSD-95) in the hippocampus were detected by immunohistochemical assay and Western blotting respectively.
Results
2
In 4 weeks after injection
the proBDNF level was significantly higher in the AAV-proBDNF group than the normal control group and the empty vector control group (
P
<
0.05). The number of DCX-positive cells in the hippocampus of AAV-proBDNF group (202.46±24.27) was significantly lower than that in the normal control group (382.26±37.58
P
<
0.05) and empty vector control group (365.48±32.68
P
<
0.05). In AAV-proBDNF group
the relative content of PSD-95 (0.62±0.05) was obviously lower than the normal control group (0.82±0.02
P
<
0.05) and vector control group (0.86±0.07
P
<
0.05).
Conclusion
2
Lateral ventricle injection of AAV-proBDNF can induce the expression of proBDNF in the brain of AD mice
and reduce the number of new neurons and synaptic plasticity in the hippocampus.
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