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Updated: Aug 26, 2026

Real Time Monitoring of Intracellular Bile Acid Dynamics Using a Genetically Encoded FRET-based Bile Acid Sensor
Published on: January 4, 2016
[On the bile acid receptor FXR]
Shuo Li1, Zhi-Wen Zhang, You-Fei Guan
1Department of Physiology, Peking University Health Science Center, Beijing 100083.
Abstract:
Farnesoid X receptor (FXR) was identified as a bile acid receptor for regulation of bile acid biosynthesis and cholesterol metabolism. FXR became a potential therapeutic target for lowering serum cholesterol and certain cardiovascular and liver diseases. In this review, the discovery of FXR, its roles in regulating bile acid and cholesterol metabolism and its application in cardiovascular disease will be summarized.
Insights
Farnesoid X receptor (FXR) regulates bile acid and cholesterol. This review summarizes FXR
Area of Science:
- Biochemistry
- Molecular Biology
- Pharmacology
Background:
- Farnesoid X receptor (FXR) identified as a key bile acid receptor.
- FXR plays a crucial role in regulating bile acid biosynthesis and cholesterol metabolism.
- FXR is implicated in cardiovascular and liver diseases.
Purpose of the Study:
- To review the discovery and biological roles of FXR.
- To explore FXR's application in managing cardiovascular diseases.
- To summarize FXR's involvement in bile acid and cholesterol homeostasis.
Main Methods:
- Literature review of FXR research.
- Analysis of studies on FXR's role in metabolism.
- Synthesis of information on FXR's therapeutic potential.
Main Results:
- FXR's discovery as a nuclear receptor activated by bile acids.
- Elucidation of FXR's function in regulating genes involved in bile acid synthesis and transport.
- Evidence supporting FXR's impact on lipid metabolism and cardiovascular health.
Conclusions:
- FXR is a critical regulator of bile acid and cholesterol metabolism.
- FXR represents a promising therapeutic target for metabolic and cardiovascular diseases.
- Further research into FXR modulation could yield novel treatments.
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