|
|
Effects of aquaporin-4 gene knockout on behavior changes and cerebral morphology during aging in mice |
SU Shengan,LU Yunbi,ZHANG Weiping |
Department of Pharmacology,Zhejiang University School of Medicine,Hangzhou 310058,China |
|
|
Abstract Objective: To investigate the effects of aquaporin-4 (AQP4) gene knockout on the behavior changes and cerebral morphology during aging in mice,and to compare that of young and aged mice between AQP4 knockout mice (AQP4-/-) and wild type mice (AQP4+/+). Methods: Fifty-eight CD-1 mice were divided into four groups:young (2-3 months old) AQP4-/-,aged (17-19 months old) AQP4-/-,young AQP4+/+ and aged AQP4+/+.The activity levels and exploring behavior of mice were tested in open field.The neurons were stained with toluidine blue and NeuN,the astrocytes and microglias were stained with GFAP and Iba-1,respectively.The morphological changes of neuron,astrocyte and microglia were then analyzed. Results: Compared with young mice,the total walking distance in open field of aged AQP4+/+ mice and aged AQP4-/- mice decreased 41.2% and 44.1%,respectively (P<0.05); while there was no difference in the ratio of distance and retention time in the central area of open field.The density of neuron in cortex of aged AQP4+/+ mice and aged AQP4-/- mice decreased 19.6% and 15.8%,respectively (P<0.05),while there was no difference in the thickness of neuron cell body in hippocampus CA1 region.The density of astrocyte in hippocampus CA3 region of aged AQP4+/+ mice and aged AQP4-/- mice increased 57.7% and 64.3%,respectively (P<0.001),while there was no difference in the area of astrocyte.The area of microglia in hippocampus CA3 region of aged AQP4+/+ mice and aged AQP4-/- mice increased 46.9% and 52.0%,respectively (P<0.01),while there was no difference in the density of microglia.Compared with AQP4+/+ mice,the young and aged AQP4-/- mice showed smaller area of astrocyte in hippocampus CA3 region,reduced 18.0% in young mice and 23.6% in aged mice.There was no difference between AQP4+/+ mice and AQP4-/- mice for other observed indexes. Conclusions: AQP4 may be involved in change of astrocyte and astrocyte-related behaviors during aging.AQP4 gene knockout may have limited effects on the change of neuron,microglia and most neuronal behaviors in aging process.
|
Received: 22 February 2013
Published: 25 May 2013
|
|
水通道蛋白4基因敲除对老年小鼠行为和脑形态变化的影响
目的:观察AQP4基因敲除(AQP4-/-)对老年小鼠行为学和脑形态学变化的影响,揭示AQP4在脑老化中的作用。方法:58只CD-1小鼠按基因型与月龄分为4组:年轻(2~3个月龄)AQP4-/-组、老年(17~19个月龄)AQP4-/-组、年轻AQP4+/+组和老年AQP4+/+组。采用开场试验测定小鼠运动量和探究行为,脑切片进行神经元特异性染色(甲苯胺蓝染色、NeuN染色)、星形胶质细胞特异性染色(GFAP染色)和小胶质细胞特异性染色(Iba-1染色),观察并计数皮层和海马神经元、星形胶质细胞、小胶质细胞的形态和数量。结果:与年轻小鼠比较,老年AQP4+/+和AQP4-/-小鼠在开场试验的总活动距离分别减少41.2%和44.1%(P<0.05),各组小鼠在中心区域的活动距离和滞留时间无差异;老年AQP4+/+和AQP4-/-小鼠皮层神经元密度分别降低19.6%和15.8%(P<0.05),各组间CA1区神经元胞体层厚度无差异;老年AQP4+/+和AQP4-/-小鼠海马CA3区星形胶质细胞密度分别增加57.7%和64.3%(P<0.001),各组间星形胶质细胞的总面积无显著差异;老年AQP4+/+和AQP4-/-小鼠海马CA3区小胶质细胞的面积分别增加46.9%和52.0%(P<0.01),各组间小胶质细胞密度无显著变化。与AQP4+/+小鼠相比,AQP4-/-小鼠在海马CA3区星形胶质细胞总面积明显减小,年轻小鼠减小18.0%(P<0.01),老年小鼠减小23.6%(P<0.01),其余指标均无显著差异。结论:AQP4可能影响小鼠星形胶质细胞形态及与星形胶质细胞相关的神经功能,对神经元、小胶质细胞的形态和部分相关神经行为无明显影响,AQP4基因敲除对小鼠脑老化过程发生的脑形态和神经行为变化无显著影响。
关键词:
水通道蛋白4/生物合成,
海马,
神经元/病理学,
小胶质细胞/病理学,
星形胶质细胞/病理学,
衰老/病理学,
小鼠,
基因敲除
|
|
\[1\]HEDDEN T,GABRIELI J D.Insights into the ageing mind:a view from cognitive neuroscience \
[J\].Nat Rev Neurosci,2004,5(2):87-96.
\[2\]MANLEY G T,BINDER D K,PAPADOPOULOS M C,et al.New insights into water transport and edema in the central nervous system from phenotype analysis of aquaporin-4 null mice \[J\].Neuroscience,2004,129(4):983-991.
\[3\]VERKMAN A S,BINDER D K,BLOCH O,et al.Three distinct roles of aquaporin-4 in brain function revealed by knockout mice \[J\].Biochim Biophys Acta,2006,1758(8):1085-1093.
\[4\]LI J,VERKMAN A S.Impaired hearing in mice lacking aquaporin-4 water channels \[J\].J Biol Chem,2001,276(33):31233-31237.
\[5\]YAO X,HRABETOVA S,NICHOLSON C,et al.Aquaporin-4-deficient mice have increased extracellular space without tortuosity change \[J\].J Neurosci,2008,28(21):5460-5464.
\[6\]NIELSEN S,NAGELHUS E A,AMIRY-MOGHADDAM M,et al.Specialized membrane domains for water transport in glial cells:high-resolution immunogold cytochemistry of aquaporin-4 in rat brain \[J\].J Neurosci,1997,17(1):171-180.
\[7\]FAN Y,ZHANG J,SUN X L,et al.Sex- and region-specific alterations of basal amino acid and monoamine metabolism in the brain of aquaporin-4 knockout mice \[J\].J Neurosci Res,2005,82(4):458-464.
\[8\]ZENG X N,SUN X L,GAO L,et al.Aquaporin-4 deficiency down-regulates glutamate uptake and GLT-1 expression in astrocytes \[J\].Mol Cell Neurosci,2007,34(1):34-39.
\[9\]PANNASCH U,VARGOVA L,REINGRUBER J,et al.Astroglial networks scale synaptic activity and plasticity \
[J\].Proc Natl Acad Sci USA,2011,108(20):8467-8472.\[10\]KONG H,SHA L L,FAN Y,et al.Requirement of AQP4 for antidepressive efficiency of fluoxetine:implication in adult hippocampal neurogenesis \[J\].Neuropsychopharmacology,2009,34(5):1263-1276.
\[11\]FAN Y,LIU M,WU X,et al.Aquaporin-4 promotes memory consolidation in Morris water maze \
[J\].Brain Struct Funct,2013,218(218):39-50.
\[12\]SKUCAS V A,MATHEWS I B,YANG J,et al.Impairment of select forms of spatial memory and neurotrophin-dependent synaptic plasticity by deletion of glial aquaporin-4 \[J\].J Neurosci,2011,31(17):6392-6397.
\[13\]SHI Wenzhen,ZHAO Chunzhen,HUANG Xueqin,et al(史文珍,赵春贞,黄雪琴,等).Deficiency of water channel AQP4 aggravates NMDA-induced brain injury in mice \[J\].J Zhejiang Univ:Medical Sci(浙江大学学报:医学版),2011,40(2):145-149.(in Chinese)
\[14\]ZHANG Weiru,HOU Fanfan,LIU Shangxi,et al(张卫茹,侯凡凡,刘尚喜,等).Advanced glycation end products accelerate atherosclerosis via enhancement of oxidative stress \[J\].Chinese Medical Journal(中华医学杂志),2004,84(13):1066-1072.(in Chinese)
\[15\]ZHOU J,KONG H,HUA X,et al.Altered blood-brain barrier integrity in adult aquaporin-4 knockout mice \
[J\].Neuroreport,2008,19(1):1-5.
\[16\]SAADOUN S,TAIT M J,REZA A,et al.AQP4 gene deletion in mice does not alter blood-brain barrier integrity or brain morphology \[J\].Neuroscience,2009,161(3):764-772.
\[17\]NICCHIA G P,SRINIVAS M,LI W,et al.New possible roles for aquaporin-4 in astrocytes:cell cytoskeleton and functional relationship with connexin43 \[J\].FASEB J,2005,19(12):1674-1676.
\[18\]FRIGERI A,GROPPER M A,UMENISHI F,et al.Localization of MIWC and GLIP water channel homologs in neuromuscular,epithelial and glandular tissues \[J\].J Cell Sci,1995,108(Pt 9):2993-3002.
\[19\]SHI W Z,ZHAO C Z,ZHAO B,et al.Aquaporin-4 deficiency attenuates acute lesions but aggravates delayed lesions and microgliosis after cryoinjury to mouse brain \[J\].Neurosci Bull,2012,28(1):61-68.
\[20\]ARIMA H,YAMAMOTO N,SOBUE K,et al.Hyperosmolar mannitol simulates expression of aquaporins 4 and 9 through a p38 mitogen-activated protein kinase-dependent pathway in rat astrocytes \[J\].J Biol Chem,2003,278(45):44525-44534.
\[21\]STURROCK R R.Changes in neuron number in the cerebellar cortex of the ageing mouse \
[J\].J Hirnforsch,1989,30(4):499-503.
\[22\]AMENTA F,BRONZETTI E,SABBATINI M,et al.Astrocyte changes in aging cerebral cortex and hippocampus:a quantitative immunohistochemical study \[J\].Microsc Res Tech,1998,43(1):29-33.
\[23\]HAYAKAWA N,KATO H and ARAKI T.Age-related changes of astorocytes,oligodendrocytes and microglia in the mouse hippocampal CA1 sector \[J\].Mech Ageing Dev,2007,128(4):311-316.
\[24\]LONG J M,KALEHUA A N,MUTH N J,et al.Stereological analysis of astrocyte and microglia in aging mouse hippocampus \[J\].Neurobiol Aging,1998,19(5):497-503.
\[25\]INGRAM D K.Age-related decline in physical activity:generalization to nonhumans \
[J\].Med Sci Sports Exerc,2000,32(9):1623-1629.
\[26\]GUPTA R K,KANUNGO M.Glial molecular alterations with mouse brain development and aging:up-regulation of the Kir4.1 and aquaporin-4 \[J\].Age (Dordr),2013,35(1):59-67.
\[27\]LEHMENKUHLER A,SYKOVA E,SVOBODA J,et al.Extracellular space parameters in the rat neocortex and subcortical white matter during postnatal development determined by diffusion analysis \
[J\].Neuroscience,1993,55(2):339-351.
\[28\]SYKOVA E,MAZEL T,SIMONOVA Z.Diffusion constraints and neuron-glia interaction during aging \
[J\].Exp Gerontol,1998,33(7-8):837-851. |
|
Viewed |
|
|
|
Full text
|
|
|
|
|
Abstract
|
|
|
|
|
Cited |
|
|
|
|
|
Shared |
|
|
|
|
|
Discussed |
|
|
|
|