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http://purl.uniprot.org/citations/22074948http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22074948http://www.w3.org/2000/01/rdf-schema#comment"Mouse resistin, a cysteine-rich protein primarily secreted from mature adipocytes, is involved in insulin resistance and type 2 diabetes. Human resistin, however, is mainly secreted by immune mononuclear cells, and it competes with lipopolysaccharide for the binding to Toll-like receptor 4, which could mediate some of the well-known proinflammatory effects of resistin in humans. In addition, resistin has been involved in the regulation of many cell differentiation and proliferation processes, suggesting that different receptors could be involved in mediating its numerous effects. Thus, a recent work identifies an isoform of Decorin (Δ Decorin) as a functional resistin receptor in adipocyte progenitors that may regulate white adipose tissue expansion. Our work shows that the mouse receptor tyrosine kinase-like orphan receptor (ROR)1 could mediate some of the described functions of resistin in 3T3-L1 adipogenesis and glucose uptake. We have demonstrated an interaction of mouse resistin with specific domains of the extracellular region of the ROR1 receptor. This interaction results in the inhibition of ROR1 phosphorylation, modulates ERK1/2 phosphorylation, and regulates suppressor of cytokine signaling 3, glucose transporter 4, and glucose transporter 1 expression. Moreover, mouse resistin modulates glucose uptake and promotes adipogenesis of 3T3-L1 cells through ROR1. In summary, our results identify mouse resistin as a potential inhibitory ligand for the receptor ROR1 and demonstrate, for the first time, that ROR1 plays an important role in adipogenesis and glucose homeostasis in 3T3-L1 cells. These data open a new line of research that could explain important questions about the resistin mechanism of action in adipogenesis and in the development of insulin resistance."xsd:string
http://purl.uniprot.org/citations/22074948http://purl.org/dc/terms/identifier"doi:10.1210/me.2011-1027"xsd:string
http://purl.uniprot.org/citations/22074948http://purl.uniprot.org/core/author"Baladron V."xsd:string
http://purl.uniprot.org/citations/22074948http://purl.uniprot.org/core/author"Laborda J."xsd:string
http://purl.uniprot.org/citations/22074948http://purl.uniprot.org/core/author"Sanchez-Solana B."xsd:string
http://purl.uniprot.org/citations/22074948http://purl.uniprot.org/core/date"2012"xsd:gYear
http://purl.uniprot.org/citations/22074948http://purl.uniprot.org/core/name"Mol Endocrinol"xsd:string
http://purl.uniprot.org/citations/22074948http://purl.uniprot.org/core/pages"110-127"xsd:string
http://purl.uniprot.org/citations/22074948http://purl.uniprot.org/core/title"Mouse resistin modulates adipogenesis and glucose uptake in 3T3-L1 preadipocytes through the ROR1 receptor."xsd:string
http://purl.uniprot.org/citations/22074948http://purl.uniprot.org/core/volume"26"xsd:string
http://purl.uniprot.org/citations/22074948http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/22074948
http://purl.uniprot.org/citations/22074948http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/22074948
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http://purl.uniprot.org/uniprot/Q9Z139http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22074948
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