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Crosstalk between KDEL receptor and EGF receptor mediates cell proliferation and migration via STAT3 signaling by Jie Jia; Lianhui Zhu; Xihua Yue; Shuocheng Tang; Shuaiyang Jing; Chuanting Tan; Yulei Du; Jingkai Gao; Intaek Lee; Yi Qian is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

What is Crosstalk between KDEL receptor and EGF receptor mediates cell proliferation and migration via STAT3 signaling about?

Hostile microenvironment of cancer cells provoke a stressful condition for endoplasmic reticulum (ER) and stimulate the expression and secretion of ER chaperones, leading to tumorigenic effects. However, the molecular mechanism underlying these effects is largely unknown. In this study, we reveal that the last four residues of ER chaperones, which are recognized by KDEL receptor (KDELR), is required for cell proliferation and migration induced by secreted chaperones. By combining proximity-based mass spectrometry analysis, split venus imaging and membrane yeast two hybrid assay, we present that EGF receptor (EGFR) may be a co-receptor for KDELR on the surface. Prior to ligand addition, KDELR spontaneously oligomerizes and constantly undergoes recycling near the plasma membrane. Upon KDEL ligand binding, the interactions of KDELR with itself and with EGFR increase rapidly, leading to augmented internalization of KDELR and tyrosine phosphorylation in the C-terminus of EGFR. STAT3, which binds the phosphorylated tyrosine motif on EGFR, is subsequently activated by EGFR and mediates cell growth and migration. Taken together, our results suggest that KDELR serves as a __bona fide__ cell

Who reads Crosstalk between KDEL receptor and EGF receptor mediates cell proliferation and migration via STAT3 signaling?

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Jie Jia; Lianhui Zhu; Xihua Yue; Shuocheng Tang; Shuaiyang Jing; Chuanting Tan; Yulei Du; Jingkai Gao; Intaek Lee; Yi Qian
Publisher
BioMed Central
Published
2024
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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