Abstract
Pleiotrophin (PTN) plays diverse roles in cell growth and differentiation. In this investigation, we demonstrate that PTN plays a negative role in adipogensis and that glycogen synthase kinase 3beta (GSK-3beta) and beta-catenin are involved in the regulation of PTN-mediated preadipocyte differentiation. Knocking down the expression of PTN using siRNA resulted in an increase in phospho-GSK-3beta expression, and the accumulation of nuclear beta-catenin, which are critical downstream signaling proteins for both the PTN and Wnt signaling pathways. Our investigation suggests that there is a PTN/PI3K/AKT/GSK-3beta/beta-catenin signaling pathway, which cross-talks with the Wnt/Fz/GSK-3beta/beta-catenin pathway and negatively regulates adipogenesis.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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3T3-L1 Cells
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Adipocytes / cytology
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Adipocytes / drug effects
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Adipocytes / metabolism
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Adipogenesis / drug effects
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Adipogenesis / genetics
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Adipogenesis / physiology*
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Animals
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Base Sequence
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Carrier Proteins / antagonists & inhibitors
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Carrier Proteins / genetics
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Carrier Proteins / physiology*
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Cell Differentiation / drug effects
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Cytokines / antagonists & inhibitors
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Cytokines / genetics
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Cytokines / physiology*
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Dexamethasone / pharmacology
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Down-Regulation / drug effects
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Gene Expression Profiling
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Mice
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Models, Biological
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PPAR gamma / metabolism
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RNA, Small Interfering / genetics
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Signal Transduction
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Wnt Proteins / metabolism
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beta Catenin / metabolism
Substances
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CTNNB1 protein, mouse
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Carrier Proteins
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Cytokines
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PPAR gamma
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RNA, Small Interfering
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Wnt Proteins
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beta Catenin
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pleiotrophin
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Dexamethasone