Adaptor protein containing PH domain, PTB domain and leucine zipper (APPL1) regulates the protein level of EGFR by modulating its trafficking

• Published in: Biochemical and biophysical research communications 2011-11, Vol.415 (1), p.206-211
• Main Authors: Lee, Jae-Rin, Hahn, Hwa-Sun, Kim, Young-Hoon, Nguyen, Hong-Hoa, Yang, Jun-Mo, Kang, Jong-Sun, Hahn, Myong-Joon
• Format: Article
• Language: English
• Subjects: 60 APPLIED LIFE SCIENCES; Adaptor Proteins, Signal Transducing - genetics; Adaptor Proteins, Signal Transducing - metabolism; ANTIGENS; APPL1; EGFR; ENERGY BEAM DEPOSITION; FSH; GROWTH FACTORS; HeLa Cells; Humans; INHIBITION; INOSITOL; LASER RADIATION; LEUCINE; NEOPLASMS; PH VALUE; Protein Transport; PULSED IRRADIATION; Rab5; rab5 GTP-Binding Proteins - antagonists & inhibitors; rab5 GTP-Binding Proteins - metabolism; Receptor, Epidermal Growth Factor - metabolism; RECEPTORS; RNA, Small Interfering - genetics; Trafficking
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2011.10.064

► APPL1 regulates the protein level of EGFR in response to EGF stimulation. ► Depletion of APPL1 accelerates the movement of EGF/EGFR from the cell surface to the perinuclear region in response to EGF. ► Knockdown of APPL1 enhances the activity of Rab5. The EGFR-mediated signaling pathway regulates multiple biological processes such as cell proliferation, survival and differentiation. Previously APPL1 (adaptor protein containing PH domain, PTB domain and leucine zipper 1) has been reported to function as a downstream effector of EGF-initiated signaling. Here we demonstrate that APPL1 regulates EGFR protein levels in response to EGF stimulation. Overexpression of APPL1 enhances EGFR stabilization while APPL1 depletion by siRNA reduces EGFR protein levels. APPL1 depletion accelerates EGFR internalization and movement of EGF/EGFR from cell surface to the perinuclear region in response to EGF treatment. Conversely, overexpression of APPL1 decelerates EGFR internalization and translocation of EGF/EGFR to the perinuclear region. Furthermore, APPL1 depletion enhances the activity of Rab5 which is involved in internalization and trafficking of EGFR and inhibition of Rab5 in APPL1-depleted cells restored EGFR levels. Consistently, APPL1 depletion reduced activation of Akt, the downstream signaling effector of EGFR and this is restored by inhibition of Rab5. These findings suggest that APPL1 is required for EGFR signaling by regulation of EGFR stabilities through inhibition of Rab5.