TRAF5 and diseases in mice and humans
Species | Diseases | Phenotypes | References |
---|---|---|---|
Human | AS | Enhanced methylation of CpG island of TRAF5 gene promoter and decreased TRAF5 gene expression in PBMCs | [31] |
RA | A SNP mapping upstream of TRAF5 gene and affecting a putative transcription factor binding site | [32] | |
Uveitis | SNPs in TRAF5 gene | [33] | |
SS | Decreased TRAF5 gene expression in the temporal bulbar conjunctiva | [35] | |
SLE | Enhanced TLR7 signaling caused by decreased expression of TRAF5 in B cells (pre-plasma cells) | [36] | |
Coronary heart disease | Decreased TRAF5 gene expression in the blood | [21] | |
Obesity with a high cardiovascular risk | Decreased TRAF5 gene expression in blood leukocytes and adipocytes | [20] | |
NAFLD | Decreased TRAF5 protein expression in the liver | [23] | |
Mouse | Allergic asthma | Enhanced Th2 responses caused by Traf5-deficiency | [18] |
EAE | Enhanced Th17 responses caused by Traf5-deficiency | [13] | |
Wound healing | Increased pDC-mediated wound repair inflammatory responses caused by Traf5-deficiency | [27] | |
Atherosclerosis | Enhanced atherosclerosis caused by Traf5-deficiency | [21] | |
Diet-induced obesity | Enhanced diet-induced obesity and inflammation in the adipose tissue caused by Traf5-deficiency | [20] | |
NAFLD | Enhanced hepatic steatosis caused by Traf5-deficiency | [23] | |
Myocardial ischemia-reperfusion injury | Exacerbated inflammation and cell death after a myocardial ischemia-reperfusion injury caused by Traf5-deficiency | [22] |
PBMCs: peripheral blood mononuclear cells
We thank the Life Science Research Center, University of Toyama and the Institute for Animal Experimentation, Tohoku University Graduate School of Medicine for technical support. We thank members of Laboratory of Molecular Cell Biology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, and Department of Microbiology and Immunology, Tohoku University Graduate School of Medicine for their assistance and help. We also thank Michael Croft and Hiroyasu Nakano for Traf5−/− mice and for their encouragement at the start of the project.
TS and NI: Supervision. TS and MHK: Writing—original draft. TS, NI and MHK: Writing—review & editing. All authors read and approved the submitted version.
The authors declare that there are no conflicts of interest.
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The study was approved by Japan Society for the Promotion of Science KAKENHI [Grants JP15H04640 (T.S.), JP18H02572 (T.S.)]. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
© The Author(s) 2023.