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10.1042/CS20200827

http://scihub22266oqcxt.onion/10.1042/CS20200827
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32706027!8299307!32706027
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suck abstract from ncbi


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pmid32706027      Clin+Sci+(Lond) 2020 ; 134 (15): 2019-2035
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  • Epidermal growth factor signaling through transient receptor potential melastatin 7 cation channel regulates vascular smooth muscle cell function #MMPMID32706027
  • Zou ZG; Rios FJ; Neves KB; Alves-Lopes R; Ling J; Baillie GS; Gao X; Fuller W; Camargo LL; Gudermann T; Chubanov V; Montezano AC; Touyz RM
  • Clin Sci (Lond) 2020[Aug]; 134 (15): 2019-2035 PMID32706027show ga
  • OBJECTIVE: Transient receptor potential (TRP) melastatin 7 (TRPM7) cation channel, a dual-function ion channel/protein kinase, regulates vascular smooth muscle cell (VSMC) Mg2+ homeostasis and mitogenic signaling. Mechanisms regulating vascular growth effects of TRPM7 are unclear, but epidermal growth factor (EGF) may be important because it is a magnesiotropic hormone involved in cellular Mg2+ regulation and VSMC proliferation. Here we sought to determine whether TRPM7 is a downstream target of EGF in VSMCs and if EGF receptor (EGFR) through TRPM7 influences VSMC function. Approach and results: Studies were performed in primary culture VSMCs from rats and humans and vascular tissue from mice deficient in TRPM7 (TRPM7+/Deltakinase and TRPM7R/R). EGF increased expression and phosphorylation of TRPM7 and stimulated Mg2+ influx in VSMCs, responses that were attenuated by gefitinib (EGFR inhibitor) and NS8593 (TRPM7 inhibitor). Co-immunoprecipitation (IP) studies, proximity ligation assay (PLA) and live-cell imaging demonstrated interaction of EGFR and TRPM7, which was enhanced by EGF. PP2 (c-Src inhibitor) decreased EGF-induced TRPM7 activation and prevented EGFR-TRPM7 association. EGF-stimulated migration and proliferation of VSMCs were inhibited by gefitinib, PP2, NS8593 and PD98059 (ERK1/2 inhibitor). Phosphorylation of EGFR and ERK1/2 was reduced in VSMCs from TRPM7+/Deltakinase mice, which exhibited reduced aortic wall thickness and decreased expression of PCNA and Notch 3, findings recapitulated in TRPM7R/R mice. CONCLUSIONS: We show that EGFR directly interacts with TRPM7 through c-Src-dependent processes. Functionally these phenomena regulate [Mg2+]i homeostasis, ERK1/2 signaling and VSMC function. Our findings define a novel signaling cascade linking EGF/EGFR and TRPM7, important in vascular homeostasis.
  • |Animals[MESH]
  • |CSK Tyrosine-Protein Kinase/metabolism[MESH]
  • |Calcium/metabolism[MESH]
  • |Cation Transport Proteins/metabolism[MESH]
  • |Epidermal Growth Factor/*metabolism[MESH]
  • |Extracellular Signal-Regulated MAP Kinases/metabolism[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Magnesium/metabolism[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Morphogenesis[MESH]
  • |Muscle, Smooth, Vascular/growth & development/*metabolism[MESH]
  • |Myocytes, Smooth Muscle/*metabolism[MESH]
  • |Phosphorylation[MESH]
  • |Primary Cell Culture[MESH]
  • |Protein Serine-Threonine Kinases/*metabolism[MESH]
  • |Rats, Inbred WKY[MESH]


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