Relationship between cardiac protein tyrosine phosphorylation and myofibrillogenesis during axolotl heart development

• Published in: Tissue & cell Vol. 35; no. 2; pp. 133 - 142
• Main Authors: Meng, F., Huang, X.P., Zajdel, R.W., Foster, D., Dawson, N., Lemanski, S.L., Zawieja, D., Dube, D.K., Lemanski, L.F.
• Format: Journal Article
• Language: English
• Published: Scotland Elsevier Ltd 01-04-2003
• Subjects: Ambystoma mexicanum; Animals; Axolotl; Blotting, Western; Cardiogenesis; Confocal microscopy; Electrophoresis, Polyacrylamide Gel; Embryo, Nonmammalian - physiology; Freshwater; Heart - embryology; Isoelectric Focusing; Microscopy, Confocal; Mutation; Myofibrils; Organ Culture Techniques; Phosphorylation; Phosphotyrosine; Phosphotyrosine - metabolism; Sarcomeres - genetics; Sarcomeres - metabolism; Confocal microscopy; Axolotl; Cardiogenesis; Myofibrils; Phosphotyrosine
• ISSN: 0040-8166; 1532-3072
• DOI: 10.1016/S0040-8166(03)00012-0

The axolotl,
Ambystoma mexicanum, is a useful system for studying embryogenesis and cardiogenesis. To understand the role of protein tyrosine phosphorylation during heart development in normal and cardiac mutant axolotl embryonic hearts, we have investigated the state of protein tyrosine residues (phosphotyrosine, P-Tyr) and the relationship between P-Tyr and the development of organized sarcomeric myofibrils by using confocal microscopy, two-dimensional isoelectric focusing (IEF)/SDS-polyacrylamide gel electrophoresis (PAGE) and immunoblotting analyses. Western blot analyses of normal embryonic hearts indicate that several proteins were significantly tyrosine phosphorylated after the initial heartbeat stage (stage 35). Mutant hearts at stages 40–41 showed less tyrosine phosphorylated staining as compared to the normal group. Two-dimensional gel electrophoresis revealed that most of the proteins from mutant hearts had a lower content of phosphorylated amino acids. Confocal microscopy of stage 35 normal hearts using phosphotyrosine monoclonal antibodies demonstrated that P-Tyr staining gradually increased being localized primarily at cell–cell boundaries and cell–extracellular matrix boundaries. In contrast, mutant embryonic hearts showed a marked decrease in the level of P-Tyr staining, especially at sites of cell–cell and cell–matrix junctions. We also delivered an anti-phosphotyrosine antibody (PY 20) into normal hearts by using a liposome-mediated delivery method, which resulted in a disruption of the existing cardiac myofibrils and reduced heartbeat rates. Our results suggest that protein tyrosine phosphorylation is critical during myofibrillogenesis and embryonic heart development in axolotls.