Two adaptor molecules, Grb2 and Shc, have been implicated in the extracellular signal-regulated kinase (ERK) activation by receptor tyrosine kinases such as the epidermal growth factor receptor (EGFR). Here we show that the EGF-mediated ERK activation is abolished by loss of Grb2, whereas this response is not affected by loss of Shc. Conversely, the EGF-mediated c-Jun N-terminal kinase (JNK) activation is dependent on Shc, but not Grb2. These findings strongly support distinct roles for Grb2 and Shc in controlling ERK and JNK activation after EGF stimulation.
机构:Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
Antonyak, MA
Moscatello, DK
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机构:Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
Moscatello, DK
Wong, AJ
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机构:
Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USAThomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
机构:Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
Antonyak, MA
Moscatello, DK
论文数: 0引用数: 0
h-index: 0
机构:Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
Moscatello, DK
Wong, AJ
论文数: 0引用数: 0
h-index: 0
机构:
Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USAThomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA