8IL7
Structure of human soluble Adenylyl Cyclase in complex with lactate
8IL7 の概要
| エントリーDOI | 10.2210/pdb8il7/pdb |
| 分子名称 | Adenylate cyclase type 10, (2S)-2-HYDROXYPROPANOIC ACID, GLYCEROL, ... (4 entities in total) |
| 機能のキーワード | sac, lyase |
| 由来する生物種 | Homo sapiens (human) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 54636.02 |
| 構造登録者 | |
| 主引用文献 | Liu, W.,Zhang, S.,Li, Q.,Wu, Y.,Jia, X.,Feng, W.,Li, Z.,Shi, Y.,Hou, Q.,Ma, J.,Liu, Y.,Gao, P.,Ganz, T.,Liu, S. Lactate modulates iron metabolism by binding soluble adenylyl cyclase. Cell Metab., 35:1597-1612.e6, 2023 Cited by PubMed Abstract: Overproduction of lactate (LA) can occur during exercise and in many diseases such as cancers. Individuals with hyperlactatemia often display anemia, decreased serum iron, and elevated hepcidin, a key regulator of iron metabolism. However, it is unknown whether and how LA regulates hepcidin expression. Here, we show LA binds to soluble adenylyl cyclase (sAC) in normal hepatocytes and affects systemic iron homeostasis in mice by increasing hepcidin expression. Comprehensive in vitro, in vivo, and in silico experiments show that the LA-sAC interaction raises cyclic adenosine monophosphate (cAMP) levels, which activates the PKA-Smad1/5/8 signaling pathway to increase hepcidin transcription. We verified this regulatory axis in wild-type mice and in mice with disordered iron homeostasis. LA also regulates hepcidin in humans at rest and subjected to extensive exercise that produce elevated LA. Our study links hyperlactatemia to iron deficiency, offering a mechanistic explanation for anemias seen in athletes and patients with lactic acidosis. PubMed: 37480842DOI: 10.1016/j.cmet.2023.06.017 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.95 Å) |
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