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Apoptosis and expression of DNA repair proteins in ischaemic brain injury in man.

作者信息

Love S, Barber R, Wilcock G K

机构信息

Department of Neuropathology, Frenchay Hospital, Bristol, UK.

出版信息

Neuroreport. 1998 Apr 20;9(6):955-9. doi: 10.1097/00001756-199804200-00001.

Abstract

We examined the timing of apoptosis and the expression of the DNA repair proteins poly(ADP-ribose) polymerase (PARP) and Ku80 in sections of frontal and temporal lobes from patients who had suffered severe brain ischaemia due to a cardiac arrent. In situ end-labelling (ISEL) was used to detect apoptotic cells, and immunohistochemistry to assess PARP and Ku80. ISEL of scattered neurons and glia was demonstrable predominantly during the first 24 h after ischaemia. PARP and Ku80 immunoreactivity increased markedly after cerebral ischaemia, PARP particularly in the regions of greatest susceptibility to hypoxic injury: the CA1 field of the hippocampus and the depths of neocortical sulci. The up-regulation of PARP is in keeping with experimental observations concerning the key role of this enzyme in mediating ischaemic cell death.

摘要

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