Testosterone enhances taurine synthesis by upregulating androgen receptor and cysteine sulfinic acid decarboxylase expressions in male mouse liver

• Published in: American journal of physiology: Gastrointestinal and liver physiology Vol. 324; no. 4; p. G295
• Main Authors: Zhang, Di, Fan, Jingjing, Liu, Hui, Qiu, Guobin, Cui, Sheng
• Format: Journal Article
• Language: English
• Published: United States 01-04-2023
• Subjects: Animals; Carboxy-Lyases - genetics; Carboxy-Lyases - metabolism; Carboxy-Lyases - pharmacology; Cysteine Dioxygenase - genetics; Cysteine Dioxygenase - metabolism; Estradiol - pharmacology; Estrogens - metabolism; Female; Liver - metabolism; Male; Mice; Receptors, Androgen - metabolism; Taurine - metabolism; Testosterone - pharmacology; cysteine sulfinate decarboxylase; taurine; androgen receptor; testosterone
• ISSN: 1522-1547
• DOI: 10.1152/ajpgi.00076.2022

Taurine is an end-product of cysteine metabolism, whereas cysteine dioxygenase (CDO) and cysteine sulfinate decarboxylase (CSAD) are key enzymes regulating taurine synthesis. Sex steroids, including estrogens and androgens, are associated with liver physiopathological processes; however, we still do not know whether taurine and sex steroids interact in regulating liver physiology and hepatic diseases, and whether there are sex differences, although our recent study shows that the estrogen is involved in regulating taurine synthesis in mouse liver. The present study was thus proposed to identify whether 17-β-estradiol and testosterone (T) play their roles by regulating CDO and CSAD expression and taurine synthesis in male mouse liver. Our results demonstrated that testosterone did not have a significant influence on CDO expression but significantly enhanced CSAD, androgen receptor (AR) expressions, and taurine levels in mouse liver, cultured hepatocytes, and HepG2 cells, whereas these effects were abrogated by AR antagonist flutamide. Furthermore, our results showed that testosterone increased CSAD-promoter-luciferase activity through the direct interaction of the AR DNA binding domain with the CSAD promoter. These findings first demonstrate that testosterone acts as an important factor to regulate sulfur amino acid metabolism and taurine synthesis through AR/CSAD signaling pathway. In addition, the in vivo and in vitro experiments showed that 17-β-estradiol has no significant effects on liver CSAD expression and taurine synthesis in male mice and suggest that the effects of sex steroids on the taurine synthesis in mouse liver have sex differences. These results are crucial for understanding the physiological functions of taurine/androgen and their interacting mechanisms in the liver.
This study demonstrates that testosterone functions to enhance taurine synthesis by interacting with androgen receptor and binding to cysteine sulfinate decarboxylase (
) promoter zone. Whereas estrogen has no significant effects either on liver CSAD expression or taurine synthesis in male mice and suggests that the effects of sex steroids on taurine synthesis in the liver have gender differences. These new findings are the potential for establishing effective protective and therapeutic strategies for liver diseases.