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Phenotypic and Functional Analysis of Activated Regulatory T Cells Isolated from Chronic Lymphocytic Choriomeningitis Virus-infected Mice
Published on: June 22, 2016
ZDHHC5 may regulate the function of NKT cells and the immune response in Meniere's disease
Ruilong Li1,2, Keguang Chen3,4
1Department of Otorhinolaryngology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, 361000, China.
Abstract:
Meniere's disease (MD) is a heterogeneous, rare inner ear disorder characterized by recurrent vertigo, fluctuating sensorineural hearing loss, tinnitus, and aural fullness. Its molecular mechanisms remain unclear due to significant clinical and immunological heterogeneity. In this study, we integrated multi‑omics genetic data to systematically screen for palmitoylation regulatory genes associated with MD risk. We first intersected 31 core palmitoylation genes with blood cis‑eQTL datasets to identify candidate expression‑related genes, then performed two‑sample Mendelian randomization (MR) to examine their genetic correlation with MD. Summary‑data‑based MR (SMR) using two independent peripheral blood eQTL cohorts (eQTLGen and GTEx) was further applied to validate robust candidate genes. Two‑sample inverse‑variance weighted (IVW) MR revealed nominally significant associations between PPT2, ZDHHC18, ZDHHC5 and MD risk. Independent SMR validation confirmed that peripheral ZDHHC5 expression was significantly correlated with MD (eQTLGen: PSMR = 0.023; GTEx: PSMR = 0.006), and a non‑significant HEIDI test ruled out strong linkage disequilibrium confounding. We further explored potential immune mediators using a two‑step MR screening framework covering 731 peripheral immune cell phenotypes. After Benjamini-Hochberg false discovery rate (FDR) correction for all immune traits to control for multiple testing, no immune cell phenotype retained an FDR < 0.05 association with MD; therefore, formal mediation analysis was not conducted. In summary, this MR‑based genetic analysis identifies ZDHHC5 as a gene associated with MD susceptibility. The potential immune regulatory axis involving NKT cells remains speculative and requires validation through large‑scale stratified immune cohort data and functional cellular/animal experiments. No definitive causal or therapeutic conclusions can be drawn from the present genetic statistical evidence alone.
Insights
This study identifies ZDHHC5 as a gene linked to Meniere
Area of Science:
- Genetics and genomics
- Inner ear disorders
- Molecular mechanisms
Background:
- Meniere's disease (MD) is a rare inner ear disorder with unclear molecular causes.
- Significant clinical and immunological heterogeneity complicates MD research.
- Palmitoylation plays a role in cellular processes, but its link to MD is unknown.
Purpose of the Study:
- To investigate the genetic association between palmitoylation regulatory genes and Meniere's disease risk.
- To identify specific genes contributing to MD susceptibility using multi-omics data.
- To explore potential immune mediators in the pathogenesis of Meniere's disease.
Main Methods:
- Integrated multi-omics genetic data, including 31 core palmitoylation genes and cis-eQTL datasets.
- Employed two-sample Mendelian randomization (MR), including inverse-variance weighted (IVW) and summary-data-based MR (SMR).
- Utilized two independent peripheral blood eQTL cohorts (eQTLGen and GTEx) for validation.
- Screened 731 peripheral immune cell phenotypes for potential mediation using a two-step MR framework.
Main Results:
- Two-sample IVW MR indicated nominal associations between PPT2, ZDHHC18, and ZDHHC5 genes and MD risk.
- SMR validation confirmed a significant correlation between peripheral ZDHHC5 expression and MD risk (eQTLGen: PSMR=0.023; GTEx: PSMR=0.006).
- A non-significant HEIDI test supported that linkage disequilibrium did not confound the ZDHHC5 association.
- No immune cell phenotypes met the FDR < 0.05 threshold for association with MD after correction.
Conclusions:
- This genetic analysis identifies ZDHHC5 as a potential susceptibility gene for Meniere's disease.
- The potential role of ZDHHC5 in immune regulation, specifically involving NKT cells, requires further investigation.
- Current genetic evidence is insufficient for definitive causal or therapeutic conclusions regarding ZDHHC5 and MD.
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