| Literature DB >> 1375192 |
B E Dwyer1, R N Nishimura, J De Vellis, T Yoshida.
Abstract
Cultured rat forebrain astrocytes contained significant amounts of immunostainable heme oxygenase-1 (HO-1) isozyme, whereas HO-1 was undetectable in spontaneously transformed rat astroglial cells (ATs). HO-1 was inducible in both cell types by heat shock and by submicromolar amounts of H2O2. Inhibition of RNA synthesis with actinomycin D or protein synthesis with cycloheximide resulted in the rapid loss of immunostainable heme oxygenase in astrocytes. Analysis of the primary structure of heme oxygenase suggests that it is a PEST protein, i.e., targeted for rapid turnover.Entities:
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Year: 1992 PMID: 1375192 DOI: 10.1002/glia.440050407
Source DB: PubMed Journal: Glia ISSN: 0894-1491 Impact factor: 7.452