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http://purl.uniprot.org/citations/27259691http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27259691http://www.w3.org/2000/01/rdf-schema#comment"Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis, invades and replicates within susceptible hosts by disturbing host antimicrobial mechanisms. Although G protein-coupled receptors (GPCRs) are involved in most physiological and pathological activities of mammalian cells, the roles of GPCRs in Mtb invasion into host cell remain elusive. Here, we report that GPR160 expression is elevated at both mRNA and protein level in macrophages in response to BCG infection. Both the PiggyBac (PB) transposon-mediated mutation of gpr160 gene in mouse primary macrophages and siRNA-mediated knockdown of GPR160 in the human macrophage cell line THP-1 markedly reduced the entry of green fluorescent protein (GFP) expressing BCG (BCG-GFP), also operative in vivo. BCG infection-induced phosphorylation of ERK1/2 was significantly reduced in gpr160 mutated (gpr160(-/-)) macrophages relative to levels observed in wild type macrophages, while inhibition of ERK by specific inhibitor or knockdown ERK1/2 by specific siRNA markedly reduced entry of BCG. Finally, lower bacteria burdens and attenuated pathological impairments were observed in the lungs of BCG-infected gpr160(-/-) mice. Furthermore, gpr160(-/-) macrophages also exhibits reduced uptake of Escherichia coli and Francisella tularensis. Taken together, these findings suggest an important role of GPR160 in regulating the entry of BCG into macrophages by targeting the ERK signaling pathway. As GPCRs have proven to be successful drug targets in pharmaceutical industry, it's tempting to speculate that compounds targeting GPR160, a G protein-coupled receptor, could intervene in Mtb infection."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.org/dc/terms/identifier"doi:10.1016/j.cellsig.2016.05.022"xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Chen J."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Chen H."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Feng Y."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Huang X."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Liu H."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Liu Z."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Liu F."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Yang H."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Zheng R."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Mo H."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/author"Ge B."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/name"Cell Signal"xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/pages"1145-1151"xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/title"G protein-coupled receptor160 regulates mycobacteria entry into macrophages by activating ERK."xsd:string
http://purl.uniprot.org/citations/27259691http://purl.uniprot.org/core/volume"28"xsd:string
http://purl.uniprot.org/citations/27259691http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27259691
http://purl.uniprot.org/citations/27259691http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27259691
http://purl.uniprot.org/uniprot/#_P63085-mappedCitation-27259691http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27259691
http://purl.uniprot.org/uniprot/#_B4DHN0-mappedCitation-27259691http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27259691
http://purl.uniprot.org/uniprot/#_O35558-mappedCitation-27259691http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27259691
http://purl.uniprot.org/uniprot/#_Q14AX2-mappedCitation-27259691http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27259691