alexa Self-Sufficient Stem Cells: Stem Cell-Derived Serotoner
ISSN: 2167-0501

Biochemistry & Pharmacology: Open Access
Open Access

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations

700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Short Communication

Self-Sufficient Stem Cells: Stem Cell-Derived Serotonergic Neurons Rely on Endogenous BDNF Release to Establish Serotonergic Networks during Terminal Differentiation

Eva Krause, Patrick Schloss and Thorsten Lau*
Biochemical Laboratory, Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, University Heidelberg, Germany
Corresponding Author : Thorsten Lau
Biochemical Laboratory
Department of Psychiatry and Psychotherapy
Central Institute of Mental Health
Medical Faculty Mannheim, University Heidelberg, Germany
Tel: +49-621- 1703-2906
Fax: +49 621 1703 6255
E-mail: [email protected]
Received September 29, 2015; Accepted October 29, 2015; Published November 03, 2015
Citation:Krause E, Schloss P, Lau T (2015) Self-Sufficient Stem Cells: Stem Cell- Derived Serotonergic Neurons Rely on Endogenous BDNF Release to Establish Serotonergic Networks during Terminal Differentiation. Biochem Pharmacol (Los Angel) 4:194. doi:10.4172/2167-0501.1000194
Copyright: ©2015 Krause E, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


The neurotransmitter serotonin plays an essential role in a variety of physiological processes including learning and memory, mood, and neuromodulation. Consequently a dysfunction of serotonergic neurotransmission is associated with psychiatric diseases such as depression, anxiety disorders, and schizophrenia. Because the small number and vast aborization of serotonergic neurons in vivo impedes their use in primary cell culture, stem cell-derived serotonergic neurons are applied as in vitro-models for serotonergic neurotransmission. Among others, 1C11 stem cells are used to generate serotonergic neurons in vitro, for example, to analyze the effect of antidepressant treatment on serotonin re-uptake or the function of microRNAs in serotonergic neurons. Since 1C11 stem cells differentiate uniformly into serotonergic neurons, there is no need to optimize terminal differentiation. Therefore the contribution of neurotrophic factors, such as the brain-derived neurotrophic factor (BDNF), to terminal differentiation of 1C11 stem cells is currently unknown. To bridge this gap, we differentiated 1C11 stem cells and determined the effect of endogenous BDNF release as well as of supplemented recombinant BDNF on neurite growth. With regard to the application of recombinant BDNF we also differentiated 1C11 stem cells in microfluidic isolation devices in order to determine whether the location of recombinant BDNF application may exert differential effects on neurite growth. Our data showed that endogenously synthesized and released BDNF is sufficient to form functional neuritic networks during terminal differentiation and that an exogenous BDNF source did not extensively promote neurite growth. However, the location of recombinant BDNF application did affect the microgrooves targeting behaviour of differentiating 1C11 stem cells in microfluidic isolation devices. In summary, our data shows that 1C11 stem cells rely on synthesis and release of endogenous BDNF for serotonergic network formation during terminal differentiation.

Share This Page

Additional Info

Loading Please wait..
Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version