Epidermal growth factor (EGF) triggers nuclear calcium signaling through the intranuclear phospholipase Cd-4 (PLCd4). Journal Article

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Authors: de Miranda, MC; Rodrigues, MA; de Angelis Campos, AC; Faria, JAQA; Kunrath-Lima, M; Mignery, GA; Schechtman, D; Goes, AM; Nathanson, MH; Gomes, DA
Article Title: Epidermal growth factor (EGF) triggers nuclear calcium signaling through the intranuclear phospholipase Cd-4 (PLCd4).
Abstract: Calcium (Ca) signaling within the cell nucleus regulates specific cellular events such as gene transcription and cell proliferation. Nuclear and cytosolic Ca 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)P) within the nucleus, leading to Ca release from the nucleoplasmic reticulum by inositol 1,4,5-trisphosphate receptors. PI(4,5)P 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 PLCd4 in epidermal growth factor (EGF)-induced nuclear Ca signaling and downstream events. We found that EGF-induced Ca signals are inhibited when translocation of EGFR is impaired. Nuclear Ca signals also were reduced by selectively buffering inositol 1,4,5-trisphosphate (InsP) within the nucleus. EGF induced hydrolysis of nuclear PI(4,5)P by the intranuclear PLCd4, rather than by PLC?1. Moreover, protein kinase C, a downstream target of EGF, was active in the nucleus of stimulated cells. Furthermore, PLCd4 and InsP 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 PLCd4 and suggest new therapeutic targets to modulate the proliferative effects of this growth factor.
Journal Title: The Journal of biological chemistry
ISSN: 1083-351X; 0021-9258
Publisher: Unknown  
Date Published: 2019