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PMID: 3001708 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Type beta transforming growth factor controls the adipogenic differentiation of 3T3 fibroblasts.

Ignotz RA, Massagué J

Abstract

Differentiating mouse 3T3-L1 preadipocytes have been used as a model system to study the ability of type beta transforming growth factor (TGF-beta) to modulate cell development. We find that TGF-beta inhibits potently (ID50 approximately equal to 25 pM) the adipogenic conversion of 3T3-L1 cells. Inhibition is observed only when cells are exposed to TGF-beta before they become committed to differentiation. Even a transient (4 hr) exposure to TGF-beta immediately before the commitment point is sufficient to prevent differentiation. This point coincides with the time point immediately preceding the onset of coordinate expression of differentiation-specific proteins in 3T3-L1 cells. TGF-beta interacts with cell surface receptors in 3T3-L1 cells that have structural and binding properties similar to TGF-beta receptors in other cell types in which TGF-beta acts as a growth activator or a growth inhibitor. However, TGF-beta does not markedly alter differentiation-related mitosis in 3T3-L1 cells. The action of TGF-beta on 3T3-L1 cells does not involve changes in cAMP or prostaglandin E levels. These results suggest that TGF-beta is a unique modulator of adipogenic differentiation of fibroblasts.

MeSH Terms
Adipose Tissue/cytology,metabolism Animals Cell Differentiation/drug effects Cell Division/drug effects Cells, Cultured Cyclic AMP/biosynthesis Dose-Response Relationship, Drug ErbB Receptors Glucosephosphate Dehydrogenase/metabolism Growth Substances/pharmacology Mice Multienzyme Complexes/metabolism Oxo-Acid-Lyases/metabolism Peptides/pharmacology Prostaglandins E/biosynthesis Receptors, Cell Surface/metabolism Time Factors Transforming Growth Factors
Chemicals
Growth Substances Multienzyme Complexes Peptides Prostaglandins E Receptors, Cell Surface Transforming Growth Factors Cyclic AMP Glucosephosphate Dehydrogenase ErbB Receptors Oxo-Acid-Lyases citrate (pro-3S)-lyase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ignotz R A
Massagué J
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25 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1985-12-00
Pages
8530-4
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC390950
Subset
IM
Grants
NCI NIH HHS · CA34610 · United States
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