Olfactory receptors contribute to progression of kidney fibrosis.
Ali MotahharyniaShiva MoeinFarnoush KiyanpourKobra MoradzadehMoein YaqubiYousof GheisariPublished in: NPJ systems biology and applications (2022)
Olfactory receptors (ORs) which are mainly known as odor-sensors in the olfactory epithelium are shown to be expressed in several non-sensory tissues. Despite the specified role of some of these receptors in normal physiology of the kidney, little is known about their potential effect in renal disorders. In this study, using the holistic view of systems biology, it was determined that ORs are significantly changed during the progression of kidney fibrosis. For further validation, common differentially expressed ORs resulted from reanalysis of two time-course microarray datasets were selected for experimental evaluation in a validated murine model of unilateral ureteral obstruction (UUO). Transcriptional analysis by real-time quantitative polymerase chain reaction demonstrated considerable changes in the expression pattern of Olfr433, Olfr129, Olfr1393, Olfr161, and Olfr622 during the progression of kidney fibrosis. For localization of these ORs, single-cell RNA-sequencing datasets of normal and UUO mice were reanalyzed. Results showed that Olfr433 is highly expressed in macrophages in day-2 and 7 post-injury in UUO mice and not in normal subgroups. Besides, like previous findings, Olfr1393 was shown to be expressed prominently in the proximal tubular cells of the kidney. In conclusion, our combinatorial temporal approach to the underlying mechanisms of chronic kidney disease highlighted the potential role of ORs in progression of fibrosis. The expression of Olfr433 in the macrophages provides some clue about its relation to molecular mechanisms promoted in the fibrotic kidney. The proposed ORs in this study could be the subject of further functional assessments in the future.
Keyphrases
- single cell
- chronic kidney disease
- poor prognosis
- rna seq
- gene expression
- induced apoptosis
- high throughput
- end stage renal disease
- adipose tissue
- skeletal muscle
- binding protein
- systemic sclerosis
- endoplasmic reticulum stress
- insulin resistance
- liver fibrosis
- mass spectrometry
- oxidative stress
- signaling pathway
- cell cycle arrest
- current status
- pi k akt
- wild type
- editorial comment
- bioinformatics analysis