Conjugated bile acids promote metabolic dysfunction-associated steatotic liver disease through inducing nuclear translocation of sphingosine-1-phosphate receptor 2 to disrupt peroxisome proliferator-activated receptor alpha

CBAs promoted MASLD through inducing S1PR2 translocation into the nucleus, where it bound PPARα to interdict the function of PPARα in regulating genes involved in lipid catabolism.

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Publication Details

Journal
Cell Communication and Signaling
Published
2025-05-25
DOI
https://doi.org/10.1186/s12964-025-02249-1
Citations
3
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
4.06

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article

Conjugated bile acids promote metabolic dysfunction-associated steatotic liver disease through inducing nuclear translocation of sphingosine-1-phosphate receptor 2 to disrupt peroxisome proliferator-activated receptor alpha

Yong Hai, Xinfeng Wu, Hui Shao, Ming Tan et al.
3 citations
Cell Communication and Signaling
Liver Disease Diagnosis and Treatment
4.06
article

Conjugated bile acids promote metabolic dysfunction-associated steatotic liver disease through inducing nuclear translocation of sphingosine-1-phosphate receptor 2 to disrupt peroxisome proliferator-activated receptor alpha

Yong Hai, Xinfeng Wu, Hui Shao, Ming Tan, Shu‐Xiang Cui, Zhao Sun, Keqin Li, Xiaohui Liu, Liang Wang, Sheng Zhan, Rong‐Rong Miao, Rui‐Hua Xu, Xian‐Jun Qu, Yuyao Cheng
article en
3 citations

Abstract

CBAs promoted MASLD through inducing S1PR2 translocation into the nucleus, where it bound PPARα to interdict the function of PPARα in regulating genes involved in lipid catabolism.

Cell Communication and SignalingVol. 23(1)
Capital Medical University (CN), China Rehabilitation Research Center (CN)
Innovative Research Group Project of the National Natural Science Foundation of China, National Natural Science Foundation of China, Ocean University of China
Openalex Percentile: Top 6%
Liver Disease Diagnosis and Treatment
4.06
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