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PMID: 2114318 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Interleukin-1 induces rapid and transient expression of the c-fos proto-oncogene in isolated pancreatic islets and in purified beta-cells.

FEBS letters ·Vol. 266 ·No. 1-2 ·1990-06-18 ·Pages 33-6

Hughes JH, Watson MA, Easom RA, Turk J, McDaniel ML

Abstract

The effect of interleukin-1 beta (IL-1) on expression of c-fos mRNA in isolated rat pancreatic islets was examined. Accumulation of c-fos mRNA was demonstrable after 30 min of exposure to IL-1, peaked by 60 min, and declined thereafter. Fluorescence-activated cell sorting (FACS) of dispersed islet cells was employed to localize the accumulation of c-fos mRNA to the beta-cell. Cycloheximide did not influence the induction of c fos mRNA by IL-1. Accumulation of c-fos mRNA therefore appears to be an early signal transduction event in the beta-cell and a component of the cellular mechanism(s) by which IL-1 influences beta-cell function.

MeSH Terms
Animals Blotting, Northern Cell Separation Cycloheximide/pharmacology Gene Expression/drug effects In Vitro Techniques Interleukin-1/pharmacology Islets of Langerhans/cytology,physiology Proto-Oncogene Proteins/genetics,metabolism Proto-Oncogene Proteins c-fos RNA, Messenger/drug effects,genetics Rats
Chemicals
Interleukin-1 Proto-Oncogene Proteins Proto-Oncogene Proteins c-fos RNA, Messenger Cycloheximide
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hughes J H
Department of Pathology, Washington University School of Medicine, Saint Louis, MO 63110.
Watson M A
Easom R A
Turk J
McDaniel M L
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1990-06-18
Pages
33-6
Language
English
Region
England
NLM ID
0155157
Subset
IM
Grants
NIDDK NIH HHS · DK-34388 · United States
NIDDK NIH HHS · K04 DDK-01553 · United States
NIGMS NIH HHS · T32 GM07200 · United States
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