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PMID: 1537885 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

TGF-beta blocks early but not late differentiation-specific gene expression and morphologic differentiation of 3T3 T proadipocytes.

Journal of cellular physiology ·Vol. 150 ·No. 3 ·1992-03-00 ·Pages 568-77

Sparks RL, Allen BJ, Strauss EE

Abstract

Transforming growth factor-beta (TGF-beta) inhibits morphologic differentiation of BALB/c 3T3 T cells as well as other proadipocyte models. Our prior studies suggested that TGF-beta may act only during the early stages of differentiation induction. However, we did not determine whether TGF-beta was differentially effecting expression of any of the various differentiation-specific genes or if it could cause down-regulation of these genes in differentiated cells. Therefore, in the current study we tested the effects of exogenous TGF-beta (0.01-5.0 ng/ml) on morphologic differentiation and on differentiation-dependent gene expression (Northern and slot blot analyses) at various times during differentiation. When induced to differentiate, 3T3 T cells first undergo predifferentiation growth arrest and from this state molecular, biochemical, and morphological differentiation proceeds. Here it was found that when added prior to the onset of differentiation, TGF-beta was a potent inhibitor or morphologic differentiation as well as of the expression of differentiation-specific genes such as lipoprotein lipase (LPL) and glycerol-3-phosphate dehydrogenase (GPD). However, once morphologic differentiation began, TGF-beta was ineffective in blocking differentiation. In addition, exposure of fully differentiated cells to TGF-beta for up to 72 hours caused no decrease of differentiation-specific genes and even a 7-day treatment caused no morphologic dedifferentiation. Tumor necrosis factor also had no detectable effect on fully differentiated cells.

MeSH Terms
3T3 Cells Adipose Tissue/cytology,drug effects,enzymology Animals Blotting, Northern Cell Differentiation/drug effects,genetics Cell Division/genetics Gene Expression Regulation, Enzymologic/drug effects Glycerolphosphate Dehydrogenase/genetics,metabolism Lipoprotein Lipase/genetics,metabolism Mice Stem Cells/cytology,drug effects,metabolism Transforming Growth Factor beta/pharmacology
Chemicals
Transforming Growth Factor beta Glycerolphosphate Dehydrogenase Lipoprotein Lipase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sparks R L
Department of Cell Biology and Anatomy, School of Medicine, Oregon Health Sciences University, Portland 97201-3098.
Allen B J
Strauss E E
Article Info
Journal
Journal of cellular physiology
Abbr.
J Cell Physiol
ISSN
0021-9541
Published
1992-03-00
Pages
568-77
Language
English
Region
United States
NLM ID
0050222
Subset
IM
Grants
NCRR NIH HHS · 2S07 RR05412 · United States
NCI NIH HHS · CA46683 · United States
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