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PMID: 1328234 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The level of CRABP-I expression influences the amounts and types of all-trans-retinoic acid metabolites in F9 teratocarcinoma stem cells.

The Journal of biological chemistry ·Vol. 267 ·No. 30 ·1992-10-25 ·Pages 21486-91

Boylan JF, Gudas LJ

Abstract

The CRABP-I and CRABP-II proteins are high affinity cytoplasmic retinoic acid-binding proteins. In undifferentiated F9 teratocarcinoma stem cells, only the CRABP-I protein is expressed at detectable levels. We have previously shown that overexpression of the CRABP-I protein in stably transfected F9 stem cell lines results in a lower sensitivity to a given external concentration of retinoic acid relative to that of untransfected F9 cells; in contrast, reduced CRABP-I expression in CRABP-I cDNA anti-sense transfected lines is associated with increased sensitivity of these lines to retinoic acid. These three types of cell lines were cultured in the presence of 50 nM [3H]retinoic acid, and the metabolism of retinoic acid was followed over the next 24 h. The results demonstrate that CRABP-I has the ability to alter both the levels and types of RA metabolites produced in the cytoplasm of differentiating embryonic stem cells. Moreover, the level of CRABP-I determines the rate of RA metabolism to 4-oxo-RA such that the higher the CRABP-I level, the faster the metabolism of [3H]retinoic acid. This is the first reported connection between the level of CRABP-I expression and intracellular RA metabolism.

MeSH Terms
Carrier Proteins/genetics,metabolism Chromatography, High Pressure Liquid DNA Receptors, Retinoic Acid Teratoma Tretinoin/analogs & derivatives,metabolism Tumor Cells, Cultured
Chemicals
Carrier Proteins Receptors, Retinoic Acid 4-oxoretinoic acid Tretinoin DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Boylan J F
Department of Pharmacology, Cornell University Medical College, New York, New York 10021.
Gudas L J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1992-10-25
Pages
21486-91
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · 1F32 CA09251-01 · United States
NCI NIH HHS · CA43796 · United States
NIDCR NIH HHS · DE10389 · United States
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