Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/196257
Type: Artigo de periódico
Title: Differentiation Of C2c12 Myoblasts Is Critically Regulated By Fak Signaling.
Author: Clemente, Carolina F M Z
Corat, Marcus A F
Saad, Sara T O
Franchini, Kleber G
Abstract: This study examined whether focal adhesion kinase (FAK) plays a role in the differentiation of C(2)C(12) myoblasts into myotubes. Differentiation of C(2)C(12) myoblasts induced by switch to differentiation culture medium was accompanied by a transient reduction of FAK phosphorylation at Tyr-397 (to approximately 50%, at 1 and 2 h), followed by an increase thereafter (to 240% up to 5 days), although FAK protein expression remained unchanged. FAK and phosphorylated FAK were found at the edge of lamellipodia in proliferating cells, whereas the later increase in FAK phosphorylation in differentiating cells was accompanied by its preferential location at the tip of well-organized actin stress fibers. Hyperexpression of FAK autophosphorylation site (Tyr-397) mutant (MT-FAK) reduced FAK phosphorylation at Tyr-397 in proliferating cells and was accompanied by reduction of cyclin D1 and increase of myogenin expression. These cells failed to progress to myotubes in differentiation medium. In contrast, hyperexpression of a wild-type FAK construction (WT-FAK) increased baseline and abolished the transient reduction of FAK phosphorylation at Tyr-397 in serum-starved C(2)C(12) cells. Cells transfected with WT-FAK failed to reduce cyclin D1 and to increase myogenin expression, as well as to progress to terminal differentiation in differentiation medium. These data indicate that FAK signaling plays a critical role in the control of cell cycle as well as in the progression of C(2)C(12) cells to terminal differentiation. Transient inhibition of FAK phosphorylation at Tyr-397 contributes to trigger the myogenic genetic program, but its later activation is also central to terminal differentiation into myotubes.
Subject: Amino Acid Sequence
Animals
Cell Differentiation
Cell Line
Cell Proliferation
Focal Adhesion Kinase 1
Focal Adhesion Protein-tyrosine Kinases
Mice
Muscle Development
Mutation
Myoblasts
Phosphorylation
Protein-tyrosine Kinases
Signal Transduction
Subcellular Fractions
Tissue Distribution
Citation: American Journal Of Physiology. Regulatory, Integrative And Comparative Physiology. v. 289, n. 3, p. R862-70, 2005-Sep.
Rights: fechado
Identifier DOI: 10.1152/ajpregu.00348.2004
Address: http://www.ncbi.nlm.nih.gov/pubmed/15890789
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File SizeFormat 
pmed_15890789.pdf996.5 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.