IndraLab
Statements
rlimsp
"Taken together, there are three mechanisms by which T. gondii prevents targeting by autophagosomes; two that are triggered during invasion of the host cell: (a) MIC3/MIC6‐dependent EGFR autophosphorylation resulting in Akt activation (Muniz‐Feliciano et al., 2013), (b) FAK‐mediated activation of Src at the level of the moving junction leading to Src‐mediated transactivation of EGFR (Y845 phosphorylation) and STAT3 signalling (Portillo et al., 2017), and (c) a third mechanism that operates at later stages of the intracellular stage of T. gondii whereby prolonged PKCα/PKCβ‐Src signalling maintains EGFR autophosphorylation that in turn appears to function via Akt (Figure 9)."
rlimsp
"Furthermore, the association of Src with Shc, Grb2 and the EGFR after angiotensin II stimulation [25], together with previously described Src-mediated phosphorylation of tyrosine residues Y845 and Y1101 of the EGFR [35,36], suggest an additional means of receptor activation utilized by GPCRs that is distinct from EGFR autophosphorylation."
rlimsp
"Although EGFR is generally activated through ligand binding and autophosphorylation of its cytoplasmic tail, it is well established that Src non-receptor TK, one of the EGFR downstream transducers, can transactivate EGFR by phosphorylating tyrosine 845 (Y845); this event may contribute to full receptor activation [13]."
rlimsp
"Src dependence of EGFR Y845 phosphorylation is well established (Biscardi ; Bromann ; Ishizawar and Parsons, 2004). However, it has been suggested that phosphorylation of Y845 on one of NSCLC-associated EGFR mutants, L861Q, represents an autophosphorylation site and is Src activity-independent based on the use of EGFR and Src inhibitors (Yang ). However, Y845 phosphorylation in EGFR L858R-expressing cells was still sensitive to Src inhibitors (Yang ). While it is reasonable that activated mutant EGFRs might acquire the ability to autophosphorylate Y845, constitutive activity of Src and the enhanced EGFR-Src interaction in mutant EGFR-expressing cells suggest that phosphorylation of Y845 is quite likely to be predominantly Src-dependent."
rlimsp
"HEK293 cells co-expressing EGFR and E-cadherin displayed EGFR phosphorylation but not in cells expressing EGFR alone upon 30 min seeding on culture dish (Supplemental Figure 4C). On further analysis, we observed that residues Y845, Y1068, Y1148 and Y1173 were readily autophosphorylated, while residue Y1086 phosphorylation was barely detectable (Figure 5D)."