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活星形胶质细胞的绿色荧光蛋白成像:缺血对星形胶质细胞影响的区域差异。

GFP imaging of live astrocytes: regional differences in the effects of ischaemia upon astrocytes.

作者信息

Shannon Clare, Salter Mike, Fern Robert

机构信息

Department of Cell Physiology and Pharmacology, University of Leicester, Leicester, UK.

出版信息

J Anat. 2007 Jun;210(6):684-92. doi: 10.1111/j.1469-7580.2007.00731.x.

Abstract

The basic division between white matter 'fibrous' astrocytes and grey matter 'protoplasmic' astrocytes is well established in terms of their morphological differences. The availability of transgenic animals with green fluorescent protein (GFP) expression restricted to specific glial cell types now provides an approach for looking at changes in cell number and morphology in the two astrocyte types in whole mount preparations. This is an important goal, as the ease of generating astrocyte cultures has led to a proliferation of studies that have examined ischaemic effects on astrocytes in vitro. This has in turn engendered a belief that astrocytes have an extraordinary resistance to ischaemic injury, a belief that runs counter to almost all the data available from in vivo and whole-mount preparations. One possible source of this confusion is the reactive changes that occur in astrocytes following injury, which include an increase in cell number that may obscure early astrocyte cell death and which has been reported to initiate within hours of an ischaemic event. However, we show here that neither white matter nor grey matter GFP(+) astrocytes exhibit any feature of reactive astrocytosis within a 180-min period of reperfusion following modelled ischaemia in neonatal whole-mount preparations. We also show that white matter astrocytes are much more sensitive to ischaemia-reperfusion injury than are grey matter astrocytes, a feature that may have high significance for developmental disorders of white matter tracts such as cerebral palsy.

摘要

白质“纤维性”星形胶质细胞与灰质“原浆性”星形胶质细胞之间基于形态学差异的基本划分已得到充分确立。现在,绿色荧光蛋白(GFP)表达仅限于特定胶质细胞类型的转基因动物的出现,为观察整装标本中两种星形胶质细胞类型的细胞数量和形态变化提供了一种方法。这是一个重要目标,因为星形胶质细胞培养的简便性导致了大量研究,这些研究在体外研究了缺血对星形胶质细胞的影响。这反过来又产生了一种观点,即星形胶质细胞对缺血损伤具有非凡的抵抗力,这种观点与几乎所有来自体内和整装标本的现有数据背道而驰。这种混淆的一个可能来源是损伤后星形胶质细胞发生的反应性变化,其中包括细胞数量的增加,这可能掩盖早期星形胶质细胞死亡,并且据报道在缺血事件发生后的数小时内就开始了。然而,我们在此表明,在新生动物整装标本模拟缺血后的180分钟再灌注期内,白质和灰质GFP(+)星形胶质细胞均未表现出反应性星形胶质细胞增生的任何特征。我们还表明,白质星形胶质细胞比灰质星形胶质细胞对缺血再灌注损伤更敏感,这一特征可能对诸如脑瘫等白质束发育障碍具有重要意义。

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本文引用的文献

1
NMDA receptors are expressed in developing oligodendrocyte processes and mediate injury.
Nature. 2005 Dec 22;438(7071):1167-71. doi: 10.1038/nature04301.
2
Emerging concepts in periventricular white matter injury.
Semin Perinatol. 2004 Dec;28(6):405-14. doi: 10.1053/j.semperi.2004.10.010.
3
Astrocytic function assessed from 1-14C-acetate metabolism after temporary focal cerebral ischemia in rats.
J Cereb Blood Flow Metab. 2005 Apr;25(4):440-50. doi: 10.1038/sj.jcbfm.9600035.
5
Ischemia: astrocytes show their sensitive side.
Prog Brain Res. 2001;132:405-11. doi: 10.1016/S0079-6123(01)32091-5.
6
8
Differential sensitivity of rat hippocampal and cortical astrocytes to oxygen-glucose deprivation injury.
Neurosci Lett. 2000 May 19;285(3):177-80. doi: 10.1016/s0304-3940(00)01056-9.
9
Astrocytic demise precedes delayed neuronal death in focal ischemic rat brain.
Brain Res Mol Brain Res. 1999 May 7;68(1-2):29-41. doi: 10.1016/s0169-328x(99)00063-7.

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