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Heat shock induces intestinal-type alkaline phosphatase in rat IEC-18 cells.

Abstract
We demonstrate a previously unknown regulation for intestinal-type alkaline phosphatase (IAP) as a heat shock protein (HSP). Heat shock to rat intestinal epithelial cells (IEC)-18 at 43 degrees C induced the expression of IAP-I and HSP72 mRNAs time dependently (<60 min) but did not induce expression of IAP-II, tissue nonspecific-type alkaline phosphatase (TNAP), or HSP90 as determined by the RT-PCR method. To confirm the identity of the IAP-I gene, we sequenced the amplification product of IAP-I and found the gene to have 99% homology with the sequence of the IAP-I gene in rat intestine. Under the subculture conditions used, no IAP protein was detected in IEC-18 cells, but it became detectable as a 62-kDa band on a Western blot after heat shock. IAP-I was also induced by sodium arsenite, which generates reactive oxygen species and is an inducer of members of the HSP family. Glutathione suppressed activating protein-1 and cAMP response element-binding protein activation caused by heat shock but did not suppress the expression of IAP-I. These results suggest that cellular stress induces the elevation of IAP-I mRNA and protein synthesis. IAP-I may play an important role as a dephosphorylating enzyme under stress conditions.
AuthorsTsuyoshi Harada, Iwao Koyama, Toshihiko Kasahara, David H Alpers, Tsugikazu Komoda
JournalAmerican journal of physiology. Gastrointestinal and liver physiology (Am J Physiol Gastrointest Liver Physiol) Vol. 284 Issue 2 Pg. G255-62 (Feb 2003) ISSN: 0193-1857 [Print] United States
PMID12388181 (Publication Type: Journal Article)
Chemical References
  • Arsenites
  • Cyclic AMP Response Element-Binding Protein
  • Heat-Shock Proteins
  • Isoenzymes
  • RNA, Messenger
  • Transcription Factors
  • Dactinomycin
  • Alkaline Phosphatase
  • Glutathione
  • arsenite
Topics
  • Alkaline Phosphatase (chemistry, metabolism)
  • Animals
  • Arsenites (pharmacology)
  • Base Sequence
  • Blotting, Western
  • Cell Line
  • Cell Nucleus (genetics)
  • Cyclic AMP Response Element-Binding Protein (metabolism)
  • Dactinomycin (pharmacology)
  • Glutathione (pharmacology)
  • Heat-Shock Proteins (chemistry, metabolism)
  • Hot Temperature
  • Intestines (enzymology)
  • Isoenzymes (chemistry, metabolism)
  • Molecular Sequence Data
  • RNA, Messenger (biosynthesis, genetics)
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factors (genetics)

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