Reciprocal inhibition between MyoD and STAT3 in the regulation of growth and differentiation of myoblasts. 2003

Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
Department of Hematology/Oncology, Osaka University Graduate School of Medicine, 2-2, Yamada-oka, Suita, Osaka 565-0871, Japan.

The development of myoblasts is regulated by various growth factors as well as by intrinsic muscle-specific transcriptional factors. In this study, we analyzed the roles for STAT3 in the growth and differentiation of myoblasts in terms of cell cycle regulation and interaction with MyoD using C2C12 cells. Here we found that STAT3 inhibited myogenic differentiation induced by low serum or MyoD as efficiently as the Ras/mitogen-activated protein kinase cascade. As for this mechanism, we found that STAT3 not only promoted cell cycle progression through the induction of c-myc but also inhibited MyoD activities through direct interaction. STAT3 inhibited not only DNA binding activities of MyoD but also its transcriptional activities. However, the inhibited transcriptional activities were restored by the supplement of p300/CBP and PCAF, suggesting that STAT3 might deprive MyoD of these transcriptional cofactors. In addition, we found that MyoD inhibited DNA binding activities of STAT3, thereby inhibiting STAT3-dependent cell growth and survival of Ba/F3 cells. These results suggest that the development of muscle cells is regulated by the coordination of cytokine signals and intrinsic transcription factors.

UI MeSH Term Description Entries
D008562 Membrane Glycoproteins Glycoproteins found on the membrane or surface of cells. Cell Surface Glycoproteins,Surface Glycoproteins,Cell Surface Glycoprotein,Membrane Glycoprotein,Surface Glycoprotein,Glycoprotein, Cell Surface,Glycoprotein, Membrane,Glycoprotein, Surface,Glycoproteins, Cell Surface,Glycoproteins, Membrane,Glycoproteins, Surface,Surface Glycoprotein, Cell,Surface Glycoproteins, Cell
D009687 Nuclear Proteins Proteins found in the nucleus of a cell. Do not confuse with NUCLEOPROTEINS which are proteins conjugated with nucleic acids, that are not necessarily present in the nucleus. Nucleolar Protein,Nucleolar Proteins,Nuclear Protein,Protein, Nuclear,Protein, Nucleolar,Proteins, Nuclear,Proteins, Nucleolar
D010766 Phosphorylation The introduction of a phosphoryl group into a compound through the formation of an ester bond between the compound and a phosphorus moiety. Phosphorylations
D011993 Recombinant Fusion Proteins Recombinant proteins produced by the GENETIC TRANSLATION of fused genes formed by the combination of NUCLEIC ACID REGULATORY SEQUENCES of one or more genes with the protein coding sequences of one or more genes. Fusion Proteins, Recombinant,Recombinant Chimeric Protein,Recombinant Fusion Protein,Recombinant Hybrid Protein,Chimeric Proteins, Recombinant,Hybrid Proteins, Recombinant,Recombinant Chimeric Proteins,Recombinant Hybrid Proteins,Chimeric Protein, Recombinant,Fusion Protein, Recombinant,Hybrid Protein, Recombinant,Protein, Recombinant Chimeric,Protein, Recombinant Fusion,Protein, Recombinant Hybrid,Proteins, Recombinant Chimeric,Proteins, Recombinant Fusion,Proteins, Recombinant Hybrid
D002453 Cell Cycle The complex series of phenomena, occurring between the end of one CELL DIVISION and the end of the next, by which cellular material is duplicated and then divided between two daughter cells. The cell cycle includes INTERPHASE, which includes G0 PHASE; G1 PHASE; S PHASE; and G2 PHASE, and CELL DIVISION PHASE. Cell Division Cycle,Cell Cycles,Cell Division Cycles,Cycle, Cell,Cycle, Cell Division,Cycles, Cell,Cycles, Cell Division,Division Cycle, Cell,Division Cycles, Cell
D002454 Cell Differentiation Progressive restriction of the developmental potential and increasing specialization of function that leads to the formation of specialized cells, tissues, and organs. Differentiation, Cell,Cell Differentiations,Differentiations, Cell
D002455 Cell Division The fission of a CELL. It includes CYTOKINESIS, when the CYTOPLASM of a cell is divided, and CELL NUCLEUS DIVISION. M Phase,Cell Division Phase,Cell Divisions,Division Phase, Cell,Division, Cell,Divisions, Cell,M Phases,Phase, Cell Division,Phase, M,Phases, M
D004247 DNA A deoxyribonucleotide polymer that is the primary genetic material of all cells. Eukaryotic and prokaryotic organisms normally contain DNA in a double-stranded state, yet several important biological processes transiently involve single-stranded regions. DNA, which consists of a polysugar-phosphate backbone possessing projections of purines (adenine and guanine) and pyrimidines (thymine and cytosine), forms a double helix that is held together by hydrogen bonds between these purines and pyrimidines (adenine to thymine and guanine to cytosine). DNA, Double-Stranded,Deoxyribonucleic Acid,ds-DNA,DNA, Double Stranded,Double-Stranded DNA,ds DNA
D004268 DNA-Binding Proteins Proteins which bind to DNA. The family includes proteins which bind to both double- and single-stranded DNA and also includes specific DNA binding proteins in serum which can be used as markers for malignant diseases. DNA Helix Destabilizing Proteins,DNA-Binding Protein,Single-Stranded DNA Binding Proteins,DNA Binding Protein,DNA Single-Stranded Binding Protein,SS DNA BP,Single-Stranded DNA-Binding Protein,Binding Protein, DNA,DNA Binding Proteins,DNA Single Stranded Binding Protein,DNA-Binding Protein, Single-Stranded,Protein, DNA-Binding,Single Stranded DNA Binding Protein,Single Stranded DNA Binding Proteins
D004347 Drug Interactions The action of a drug that may affect the activity, metabolism, or toxicity of another drug. Drug Interaction,Interaction, Drug,Interactions, Drug

Related Publications

Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
April 2010, Journal of cellular physiology,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
March 1992, The Journal of cell biology,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
February 1989, Journal of cellular physiology,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
August 2008, The Journal of biological chemistry,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
November 2009, Journal of bacteriology,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
March 1985, Biochimica et biophysica acta,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
April 2001, Cellular and molecular life sciences : CMLS,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
April 2009, Cytokine,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
October 2010, The Journal of cell biology,
Yoshihisa Kataoka, and Itaru Matsumura, and Sachiko Ezoe, and Soichi Nakata, and Eri Takigawa, and Yusuke Sato, and Akira Kawasaki, and Takashi Yokota, and Koichi Nakajima, and Armando Felsani, and Yuzuru Kanakura
March 2008, International journal of biomedical science : IJBS,
Copied contents to your clipboard!