Ischemia Induces the Expression of the Platelet-Derived Growth Factor-B Chain in Neurons and Brain Macrophages in vivo
Author(s) -
Koji Iihara,
Masakiyo Sasahara,
Nobuo Hashimoto,
Yoshihiko Uemura,
Haruhiko Kikuchi,
Fumitada Hazama
Publication year - 1994
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/jcbfm.1994.102
Subject(s) - immunostaining , ischemia , immunohistochemistry , in vivo , platelet derived growth factor , neocortex , platelet derived growth factor receptor , brain ischemia , pathology , growth factor , biology , medicine , endocrinology , neuroscience , receptor , microbiology and biotechnology
To elucidate the role of the platelet-derived growth factor (PDGF)–B chain in the brain, we examined its expression in rat brains with focal ischemia. Focal ischemia was induced by permanent tandem occlusion of the middle cerebral and common carotid arteries in spontaneously hypertensive rats (SHRs). Northern analysis demonstrated that ischemia transiently increased mRNA expression of the PDGF–B chain, but not the PDGF–A chain, in the injured neocortex. The larger transcript (3.5 kb) of the B chain gradually increased to threefold by 16 h, whereas the smaller transcript (2.6 kb) of the B chain markedly increased sixfold by 4 h. Immunohistochemistry revealed enhanced immunoreactivity in the neurons in the infarct and in the periinfarct area from 16 h to days 4–7, with a peak at 24 h. Furthermore, the brain macrophages that accumulated in the infarct showed intense immunostaining in their perinuclear region from days 2 to 14, with a peak at days 5–6. The present study demonstrates that ischemia induces the expression of the PDGF–B chain, first in neurons and later in brain macrophages, and suggests an important role of the PDGF–B chain in the healing process of the injured brain.
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