MRGPRX4 is a bile acid receptor for human cholestatic itch

Author:

Yu Huasheng123ORCID,Zhao Tianjun123,Liu Simin1,Wu Qinxue4,Johnson Omar4,Wu Zhaofa12,Zhuang Zihao1,Shi Yaocheng5,Peng Luxin5,He Renxi12,Yang Yong6,Sun Jianjun7,Wang Xiaoqun8,Xu Haifeng9,Zeng Zheng10,Zou Peng5ORCID,Lei Xiaoguang35,Luo Wenqin4ORCID,Li Yulong12311ORCID

Affiliation:

1. State Key Laboratory of Membrane Biology, Peking University School of Life Sciences, Beijing, China

2. PKU-IDG/McGovern Institute for Brain Research, Beijing, China

3. Peking-Tsinghua Center for Life Sciences, Beijing, China

4. Department of Neuroscience, Perelman School of Medicine, University of Pennsylvania, Philadelphia, United States

5. Department of Chemical Biology, College of Chemistry and Molecular Engineering, Peking University, Beijing, China

6. Department of Dermatology, Beijing Key Laboratory of Molecular Diagnosis on Dermatoses, Peking University First Hospital, Peking University, Beijing, China

7. Department of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, China

8. State Key Laboratory of Brain and Cognitive Science, CAS Center for Excellence in Brain Science and Intelligence Technology (Shanghai), Institute of Biophysics, Chinese Academy of Sciences, Beijing, China

9. Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China

10. Department of Infectious Diseases, Peking University First Hospital, Beijing, China

11. Chinese Institute for Brain Research, Beijing, China

Abstract

Patients with liver diseases often suffer from chronic itch, yet the pruritogen(s) and receptor(s) remain largely elusive. Here, we identify bile acids as natural ligands for MRGPRX4. MRGPRX4 is expressed in human dorsal root ganglion (hDRG) neurons and co-expresses with itch receptor HRH1. Bile acids elicited Ca2+ responses in cultured hDRG neurons, and bile acids or a MRGPRX4 specific agonist induced itch in human subjects. However, a specific agonist for another bile acid receptor TGR5 failed to induce itch in human subjects and we find that human TGR5 is not expressed in hDRG neurons. Finally, we show positive correlation between cholestatic itch and plasma bile acids level in itchy patients and the elevated bile acids is sufficient to activate MRGPRX4. Taken together, our data strongly suggest that MRGPRX4 is a novel bile acid receptor that likely underlies cholestatic itch in human, providing a promising new drug target for anti-itch therapies.

Funder

Department of the Central Committee of the CPC

Chinese Institute for Brain Research

University of Pennsylvania

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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