Upregulation of phospholipase D in astrocytes in response to transient forebrain ischemia.

Abstract:

:Previous in vitro studies using cell cultures or brain slices have demonstrated that phospholipase D (PLD) in the nervous system is involved in the signaling mechanism in response to a variety of agonists. However, little is known about the pathophysiological role of PLD-mediated signaling in the adult brain. We examined the changes in the expression of a PLD isozyme, PLD1, in the adult rat hippocampus, using immunological approaches and an assay for PLD activity after transient forebrain ischemia (four-vessel occlusion model) that results in the selective delayed death of CA1 pyramidal cells and induces reactive astrocytes in the CA1 subfield. In the control hippocampus, PLD1 the level of immunoreactivity was very low. After ischemia, in parallel with the results of Western blot analysis and the PLD activity assay, immunohistochemical analysis of PLD1 demonstrated that the immunoreactive proteins peaked at 7-14 days and were most prominent in the CA1 and the dentate hilar region. The temporal and spatial patterns of immunoreactivity of both PLD1 and glial fibrillary acidic protein (GFAP) were very similar, indicating that reactive astrocytes express PLD1, confirmed by double staining for PLD1 and GFAP. These results demonstrate that reactive astrocytes upregulate PLD in vivo after injury in the adult rat hippocampus.

journal_name

Glia

journal_title

Glia

authors

Lee MY,Kim SY,Min DS,Choi YS,Shin SL,Chun MH,Lee SB,Kim MS,Jo YH

doi

10.1002/(sici)1098-1136(200005)30:3<311::aid-glia1

subject

Has Abstract

pub_date

2000-05-01 00:00:00

pages

311-7

issue

3

eissn

0894-1491

issn

1098-1136

pii

10.1002/(SICI)1098-1136(200005)30:3<311::AID-GLIA1

journal_volume

30

pub_type

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