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.

Highlights

  • We have recently described a simple approach to assessing changes in the density of green fluorescent protein (GFP) (+)

  • Differential sensitivity to ischemic conditions between gray matter astrocyte populations are apparent in cell culture studies (Zhao and Flavin, 2000; Xu et al, 2001), such studies always require very protracted periods of modeled ischemia and reperfusion to generate significant cell death at all

  • Astrocyte Injury evoked by ischemic-type conditions in vitro, in whole mount, and in vivo

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Summary

Concluding remarks ee

The mechanisms of acute injury of neonatal white matter astrocytes depends upon the maturity of the tissue. On reactive changes at this latter developmental stage following a limited ischemic challenge shown in the current study does not appear to be unique to the white ly matter since a similar absence of reactive changes was found in their gray matter cousins. It does appear, that the astrocytes of actively myelinating white matter have a much heightened sensitivity to ischemic-type injury, in particular in the reperfusion period after a brief period of an ischemic-type condition. Astrocyte Injury evoked by ischemic-type conditions in vitro, in whole mount, and in vivo

Method ev Astrocyte
Materials and Methods for original data w
References ee
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