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Serotonin-specific neurons differentiated from human iPSCs form distinct subtypes with synaptic protein assembly

Please always quote using this URN: urn:nbn:de:bvb:20-opus-268519
  • Human induced pluripotent stem cells (hiPSCs) have revolutionized the generation of experimental disease models, but the development of protocols for the differentiation of functionally active neuronal subtypes with defined specification is still in its infancy. While dysfunction of the brain serotonin (5-HT) system has been implicated in the etiology of various neuropsychiatric disorders, investigation of functional human 5-HT specific neurons in vitro has been restricted by technical limitations. We describe an efficient generation ofHuman induced pluripotent stem cells (hiPSCs) have revolutionized the generation of experimental disease models, but the development of protocols for the differentiation of functionally active neuronal subtypes with defined specification is still in its infancy. While dysfunction of the brain serotonin (5-HT) system has been implicated in the etiology of various neuropsychiatric disorders, investigation of functional human 5-HT specific neurons in vitro has been restricted by technical limitations. We describe an efficient generation of functionally active neurons from hiPSCs displaying 5-HT specification by modification of a previously reported protocol. Furthermore, 5-HT specific neurons were characterized using high-end fluorescence imaging including super-resolution microscopy in combination with electrophysiological techniques. Differentiated hiPSCs synthesize 5-HT, express specific markers, such as tryptophan hydroxylase 2 and 5-HT transporter, and exhibit an electrophysiological signature characteristic of serotonergic neurons, with spontaneous rhythmic activities, broad action potentials and large afterhyperpolarization potentials. 5-HT specific neurons form synapses reflected by the expression of pre- and postsynaptic proteins, such as Bassoon and Homer. The distribution pattern of Bassoon, a marker of the active zone along the soma and extensions of neurons, indicates functionality via volume transmission. Among the high percentage of 5-HT specific neurons (~ 42%), a subpopulation of CDH13 + cells presumably designates dorsal raphe neurons. hiPSC-derived 5-HT specific neuronal cell cultures reflect the heterogeneous nature of dorsal and median raphe nuclei and may facilitate examining the association of serotonergic neuron subpopulations with neuropsychiatric disorders.show moreshow less

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Metadaten
Author: Charline Jansch, Georg C. Ziegler, Andrea Forero, Sina Gredy, Sina Wäldchen, Maria Rosaria Vitale, Evgeniy Svirin, Johanna E. M. Zöller, Jonas Waider, Katharina Günther, Frank Edenhofer, Markus Sauer, Erhard Wischmeyer, Klaus-Peter Lesch
URN:urn:nbn:de:bvb:20-opus-268519
Document Type:Journal article
Faculties:Medizinische Fakultät / Physiologisches Institut
Medizinische Fakultät / Klinik und Poliklinik für Psychiatrie, Psychosomatik und Psychotherapie
Fakultät für Biologie / Theodor-Boveri-Institut für Biowissenschaften
Language:English
Parent Title (English):Journal of Neural Transmission
ISSN:1435-1463
Year of Completion:2021
Volume:128
Issue:2
Pagenumber:225-241
Source:Journal of Neural Transmission 2021, 128(2):225-241. DOI: 10.1007/s00702-021-02303-5
DOI:https://doi.org/10.1007/s00702-021-02303-5
Pubmed Id:https://pubmed.ncbi.nlm.nih.gov/33560471
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Tag:Cadherin-13 (CDH13); human induced pluripotent stem cell (hiPSC); median and dorsal raphe; neuropsychiatric disorders; serotonin-specific neurons; synapse formation
Release Date:2022/06/08
EU-Project number / Contract (GA) number:602805
EU-Project number / Contract (GA) number:728018
OpenAIRE:OpenAIRE
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International