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MicroRNA Expression Profiles of Human iPS Cells, Retinal Pigment Epithelium Derived From iPS, and Fetal Retinal Pigment Epithelium
Published on: June 24, 2014
Key molecular networks underlying retinol's biphasic effects on cell proliferation through multi-omics integrative
Peishuang He1,2, Guangming Xiang1, Yizhen Yan3,4
1State Key Laboratory of Microbial Metabolism, School of Life Science and Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, PR China.
Abstract:
Retinol is widely used in skin anti-aging, yet its effects exhibit significant concentration dependence. However, the underlying biphasic mechanism, that is low concentrations promote cell proliferation while high concentrations are inhibitory, remains incompletely understood. Here, we employed multi-omics analysis and genome-scale metabolic models (GEMs) to systematically infer the key molecular networks underlying the distinct effects of retinol concentrations on human foreskin fibroblasts (HFFs). Our results suggest that low retinol concentrations appear to promote proliferation by activating the canonical retinoic acid signaling pathway and inducing sophisticated metabolic reprogramming. This reprogramming appears to involve prioritizing the coenzyme NADPH for retinol processing and antioxidant defense, which is associated with a compensatory suppression of NADPH-consuming cholesterol biosynthesis. This metabolic shift may foster a favorable intracellular environment for growth. Conversely, high concentrations are linked to a multi-system injury cascade. The observed key feature likely involves significant oxidative stress, associated with the buildup of toxic metabolic intermediates and a pro-inflammatory lipid storm marked by elevated leukotrienes. These stress responses align with the signatures of ferroptosis, a form of programmed cell death characterized by glutathione (GSH) defense system collapse and downregulation of the key regulator GPX4. Our findings suggest a potential mechanistic transition from a state of metabolic optimization to the activation of stress-induced injury pathways in response to varying retinol concentrations. This study provides a systems-level framework for understanding retinol's biphasic effects and highlights key regulatory nodes (e.g., DHRS3, GCLM) as potential targets for future research. These insights could contribute to developing safer and more effective retinol-based formulations in cosmetic and dermatological applications.
Insights
Low retinol concentrations promote skin cell growth by optimizing metabolism, while high concentrations cause cell injury via oxidative stress and ferroptosis. Understanding this biphasic mechanism is key for safer retinol formulations.
Area of Science:
- Dermatology and Molecular Biology
- Systems Biology and Bioinformatics
- Metabolic Engineering
Background:
- Retinol is a popular anti-aging ingredient, but its effects vary with concentration.
- The precise mechanisms behind retinol's dual action (promoting growth at low doses, inhibiting at high doses) are not fully understood.
Purpose of the Study:
- To elucidate the molecular networks and metabolic reprogramming responsible for retinol's concentration-dependent effects on human foreskin fibroblasts (HFFs).
- To identify key regulatory pathways and potential therapeutic targets for optimizing retinol-based skincare.
Main Methods:
- Multi-omics analysis (genomics, transcriptomics, metabolomics) integrated with genome-scale metabolic models (GEMs).
- Systematic inference of molecular networks and metabolic pathways affected by varying retinol concentrations.
Main Results:
- Low retinol concentrations activate retinoic acid signaling and metabolic reprogramming, prioritizing NADPH for retinol processing and antioxidant defense, while suppressing cholesterol synthesis.
- High retinol concentrations induce oxidative stress, toxic metabolite accumulation, and a pro-inflammatory lipid storm, leading to ferroptosis.
- Key regulatory nodes such as DHRS3 and GCLM were identified as crucial in retinol's biphasic response.
Conclusions:
- Retinol exhibits a concentration-dependent biphasic mechanism, transitioning from metabolic optimization for proliferation to stress-induced injury pathways.
- The study provides a systems-level understanding of retinol's effects, highlighting potential targets for developing safer and more effective dermatological and cosmetic applications.
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