Platelet-Derived Serotonin Mediates Liver Regeneration

Author:

Lesurtel Mickael12345,Graf Rolf12345,Aleil Boris12345,Walther Diego J.12345,Tian Yinghua12345,Jochum Wolfram12345,Gachet Christian12345,Bader Michael12345,Clavien Pierre-Alain12345

Affiliation:

1. Department of Visceral and Transplantation Surgery, University Hospital of Zurich, Switzerland.

2. Department of Pathology, University Hospital of Zurich, Switzerland.

3. Institut National de la Santé et de la Recherche Médicale 311, Etablissement Français du Sang-Alsace, Strasbourg, France.

4. Max Planck Institute for Molecular Genetics, Berlin, Germany.

5. Max Delbrück Center for Molecular Medicine, Berlin, Germany.

Abstract

The liver can regenerate its volume after major tissue loss. In a mouse model of liver regeneration, thrombocytopenia, or impaired platelet activity resulted in the failure to initiate cellular proliferation in the liver. Platelets are major carriers of serotonin in the blood. In thrombocytopenic mice, a serotonin agonist reconstituted liver proliferation. The expression of 5-HT2A and 2B subtype serotonin receptors in the liver increased after hepatectomy. Antagonists of 5-HT2A and 2B receptors inhibited liver regeneration. Liver regeneration was also blunted in mice lacking tryptophan hydroxylase 1, which is the rate-limiting enzyme for the synthesis of peripheral serotonin. This failure of regeneration was rescued by reloading serotonin-free platelets with a serotonin precursor molecule. These results suggest that platelet-derived serotonin is involved in the initiation of liver regeneration.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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