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Tryptophan Hydroxylase-2-Mediated Serotonin Biosynthesis Suppresses Cell Reprogramming into Pluripotent State

Title: Tryptophan Hydroxylase-2-Mediated Serotonin Biosynthesis Suppresses Cell Reprogramming into Pluripotent State
Authors: Sergey A. Sinenko; Andrey A. Kuzmin; Elena V. Skvortsova; Sergey V. Ponomartsev; Evgeniya V. Efimova; Michael Bader; Natalia Alenina; Alexey N. Tomilin
Source: International Journal of Molecular Sciences, Vol 24, Iss 5, p 4862 (2023)
Publisher Information: MDPI AG
Publication Year: 2023
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: serotonin; 5-HT; pluripotency; reprogramming; induced pluripotent stem cells (iPSCs); tryptophan hydroxylase 1 and 2 (TPH1 and TPH2); Biology (General); QH301-705.5; Chemistry; QD1-999
Description: The monoamine neurotransmitter serotonin (5-hydroxytryptamine, 5-HT) has important functions both in the neural system and during embryonic development in mammals. In this study, we set out to investigate whether and how endogenous serotonin affects reprogramming to pluripotency. As serotonin is synthesized from tryptophan by the rate limiting enzymes tryptophan hydroxylase-1 and -2 (TPH1 and TPH2), we have assessed the reprogramming of TPH1- and/or TPH2-deficient mouse embryonic fibroblasts (MEFs) to induced pluripotent stem cells (iPSCs). The reprogramming of the double mutant MEFs showed a dramatic increase in the efficiency of iPSC generation. In contrast, ectopic expression of TPH2 alone or in conjunction with TPH1 reverted the rate of reprogramming of the double mutant MEFs to the wild-type level and besides, TPH2 overexpression significantly suppressed reprogramming of wild-type MEFs. Our data thus suggest a negative role of serotonin biosynthesis in the reprogramming of somatic cells to a pluripotent state.
Document Type: article in journal/newspaper
Language: English
Relation: https://www.mdpi.com/1422-0067/24/5/4862; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067; https://doaj.org/article/2155db7bd6a245439ae46e6bba42ecc0
DOI: 10.3390/ijms24054862
Availability: https://doi.org/10.3390/ijms24054862; https://doaj.org/article/2155db7bd6a245439ae46e6bba42ecc0
Accession Number: edsbas.386CEC29
Database: BASE