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Epidermal growth factor (EGF) triggers nuclear calcium signaling through the intranuclear phospholipase C?-4 (PLC?4).


ABSTRACT: Calcium (Ca2+) signaling within the cell nucleus regulates specific cellular events such as gene transcription and cell proliferation. Nuclear and cytosolic Ca2+ levels can be independently regulated, and nuclear translocation of receptor tyrosine kinases (RTKs) is one way to locally activate signaling cascades within the nucleus. Nuclear RTKs, including the epidermal growth factor receptor (EGFR), are important for processes such as transcriptional regulation, DNA-damage repair, and cancer therapy resistance. RTKs can hydrolyze phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) within the nucleus, leading to Ca2+ release from the nucleoplasmic reticulum by inositol 1,4,5-trisphosphate receptors. PI(4,5)P2 hydrolysis is mediated by phospholipase C (PLC). However, it is unknown which nuclear PLC isoform is triggered by EGFR. Here, using subcellular fractionation, immunoblotting and fluorescence, siRNA-based gene knockdowns, and FRET-based biosensor reporter assays, we investigated the role of PLC?4 in epidermal growth factor (EGF)-induced nuclear Ca2+ signaling and downstream events. We found that EGF-induced Ca2+ signals are inhibited when translocation of EGFR is impaired. Nuclear Ca2+ signals also were reduced by selectively buffering inositol 1,4,5-trisphosphate (InsP3) within the nucleus. EGF induced hydrolysis of nuclear PI(4,5)P2 by the intranuclear PLC?4, rather than by PLC?1. Moreover, protein kinase C, a downstream target of EGF, was active in the nucleus of stimulated cells. Furthermore, PLC?4 and InsP3 modulated cell cycle progression by regulating the expression of cyclins A and B1. These results provide evidence that EGF-induced nuclear signaling is mediated by nuclear PLC?4 and suggest new therapeutic targets to modulate the proliferative effects of this growth factor.

SUBMITTER: de Miranda MC 

PROVIDER: S-EPMC6851314 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Epidermal growth factor (EGF) triggers nuclear calcium signaling through the intranuclear phospholipase Cδ-4 (PLCδ4).

de Miranda Marcelo Coutinho MC   Rodrigues Michele Angela MA   de Angelis Campos Ana Carolina AC   Faria Jerusa Araújo Quintão Arantes JAQA   Kunrath-Lima Marianna M   Mignery Gregory A GA   Schechtman Deborah D   Goes Alfredo Miranda AM   Nathanson Michael H MH   Gomes Dawidson A DA  

The Journal of biological chemistry 20190919 45


Calcium (Ca<sup>2+</sup>) signaling within the cell nucleus regulates specific cellular events such as gene transcription and cell proliferation. Nuclear and cytosolic Ca<sup>2+</sup> levels can be independently regulated, and nuclear translocation of receptor tyrosine kinases (RTKs) is one way to locally activate signaling cascades within the nucleus. Nuclear RTKs, including the epidermal growth factor receptor (EGFR), are important for processes such as transcriptional regulation, DNA-damage r  ...[more]

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