Häussinger D, Schmitt M, Weiergräber O, Kubitz R
Medizinische Universitätsklinik, Heinrich Heine Universität, Düsseldorf, Germany.
Semin Liver Dis. 2000;20(3):307-21. doi: 10.1055/s-2000-9386.
On a short term basis, canalicular secretion is under control of the hepatocellular hydration state, substrates, cytokines, toxins, and hormones. Regulation occurs at the level of substrate availability, covalent modification of transporters, and their regulated exocytic insertion into or endocytic retrieval from the membrane. A variety of signal transduction pathways involving the activation of mitogen-activated protein kinases, protein kinases A and C, participates in these processes. However, much has still to be learned about the crosstalk of different signaling systems and their molecular targets that determine the outcome for canalicular secretion.
短期内,胆小管分泌受肝细胞水合状态、底物、细胞因子、毒素和激素的控制。调节发生在底物可用性、转运蛋白的共价修饰以及它们受调节的胞吐插入膜或胞吞从膜回收的水平。涉及丝裂原活化蛋白激酶、蛋白激酶A和C激活的多种信号转导途径参与这些过程。然而,关于不同信号系统的相互作用及其决定胆小管分泌结果的分子靶点,仍有许多有待了解之处。