Results

RDF/XMLNTriplesTurtleShow queryShare ▶
SubjectPredicateObject
http://purl.uniprot.org/citations/38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/38013040http://www.w3.org/2000/01/rdf-schema#comment"Infections are often accompanied by weight loss caused by alterations in host behavior and metabolism, also known as sickness behaviors. Recent studies have revealed that sickness behaviors can either promote or impede survival during infections depending on factors such as the type of infectious pathogen. Nevertheless, we have an incomplete understanding of the underlying mechanisms of sickness behaviors. Furthermore, although the host immune responses to infections have long been known to contribute to the induction of sickness behaviors, recent studies have identified emerging cytokines that are also key regulators of host metabolism during infection and inflammation, such as growth differentiation factor 15 (GDF-15). GDF-15 is a distant member of the TGF-β superfamily that causes weight loss by suppressing appetite and food consumption and causing emesis. These effects require activation of neurons that express the only known GDF-15 receptor, the GFRAL receptor. GDF-15 also functions in the periphery including the induction of ketogenesis and immunoregulation. Nevertheless, the functions and regulation of GDF-15 during live infections is not yet known. Murine infection with avirulent Toxoplasma gondii is an established model to understand infection-induced weight loss. Past studies have determined that acute T. gondii infection causes weight loss due to diminished food consumption and increased energy expenditure through unknown mechanisms. Additionally, our lab previously demonstrated that T. gondii causes upregulation in serum GDF-15 in an IFN-γ-dependent manner during the post-acute phase of the infection. In this study, we interrogated the in-vivo functions and immune regulation of GDF-15 during Toxoplasma gondii infection. First, we found that in wild-type mice, acute T. gondii infection caused a significant weight loss that is preceded by elevation of serum levels of IFN-γ and GDF-15. To determine whether IFN-γ regulates GDF-15, we neutralized IFN-γ on days 5 and 6 and measured GDF-15 on day 7 and found that serum but not tissue levels of GDF-15 decreased after IFN-γ neutralization. Additionally, exogenous IFN-γ was sufficient to elevate serum GDF-15 in the absence of infection. Next, we compared the outcomes of T. gondii infection between WT and Gdf15-/- mice. We observed that the weight trajectories were declining in WT mice while they were increasing in Gdf15-/-mice during the acute phase of the infection. This difference in trajectories extended throughout the chronic infection resulting to an overall weight loss relative to initial weights in WT mice but not Gdf15-/-mice. Then, we determined that GDF-15 is not essential for survival and immunoregulation during T. gondii infection. We also demonstrated that GDF-15 is required for the induction of FGF21, stress-induced cytokine with prominent roles in regulating host metabolism. Finally, we discovered a cytokine cascade IFN-γ-GDF-15-FGF21 that is likely involved in the regulation of host metabolism. Overall, our study provides evidence that IFN-γ contributes to the regulation of host metabolism during infection by inducing GDF-15 and FGF21. GDF-15 orchestrates changes in host metabolism that supports the host immune response in clearing the infection. These physiological alterations induce FGF21, which in turn, orchestrates the adaptive responses to the effects of GDF-15, which can be detrimental when protracted."xsd:string
http://purl.uniprot.org/citations/38013040http://purl.org/dc/terms/identifier"doi:10.1016/j.bbi.2023.11.029"xsd:string
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/author"Zhao Y."xsd:string
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/author"Reyes J."xsd:string
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/author"Yap G.S."xsd:string
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/author"Pandya K."xsd:string
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/date"2024"xsd:gYear
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/name"Brain Behav Immun"xsd:string
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/pages"24-33"xsd:string
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/title"Growth differentiation factor-15 is an IFN-gamma regulated mediator of infection-induced weight loss and the hepatic FGF21 response."xsd:string
http://purl.uniprot.org/citations/38013040http://purl.uniprot.org/core/volume"116"xsd:string
http://purl.uniprot.org/citations/38013040http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/38013040
http://purl.uniprot.org/citations/38013040http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/38013040
http://purl.uniprot.org/uniprot/#_A0A7R8C347-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_A0A7U3L6A3-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_A3RL32-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_C4NUL9-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_C4NUM1-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_P01580-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_Q3TU76-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_Q3UNI4-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_Q9JJN1-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_Q6TDH0-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
http://purl.uniprot.org/uniprot/#_Q9Z0J7-mappedCitation-38013040http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38013040
▶