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Generation and Characterization of Functional Human Hypothalamic Neurons.

Accepted version
Peer-reviewed

Type

Article

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Authors

Jura, Magdalena 
Merkle, Florian T 

Abstract

Neurons in the hypothalamus orchestrate homeostatic physiological processes and behaviors essential for life. Defects in the function of hypothalamic neurons cause a spectrum of human diseases, including obesity, infertility, growth defects, sleep disorders, social disorders, and stress disorders. These diseases have been studied in animal models such as mice, but the rarity and relative inaccessibility of mouse hypothalamic neurons and species-specific differences between mice and humans highlight the need for human cellular models of hypothalamic diseases. We and others have developed methods to differentiate human pluripotent stem cells (hPSCs) into hypothalamic neurons and related cell types, such as astrocytes. This protocol builds on published studies by providing detailed step-by-step instructions for neuronal differentiation, quality control, long-term neuronal maintenance, and the functional interrogation of hypothalamic cells by calcium imaging. Together, these protocols should enable any group with appropriate facilities to generate and study human hypothalamic cells. © 2017 by John Wiley & Sons, Inc.

Description

Keywords

POMC, differentiation, human, hypothalamus, neuron, obesity, pluripotent stem cell, protocol, Agouti-Related Protein, Bone Morphogenetic Proteins, Cell Culture Techniques, Cell Differentiation, Cells, Cultured, Enzyme Inhibitors, Humans, Hypothalamic Hormones, Hypothalamus, Neurogenesis, Neurons, Pluripotent Stem Cells, Pro-Opiomelanocortin, Signal Transduction, Time Factors

Journal Title

Curr Protoc Neurosci

Conference Name

Journal ISSN

1934-8584
1934-8576

Volume Title

81

Publisher

Wiley
Sponsorship
Wellcome Trust (100574/Z/12/Z)
Medical Research Council (MC_UU_12012/5)
Wellcome Trust (105602/Z/14/Z)
Academy of Medical Sciences (Springboard)
Medical Research Council (MC_PC_12009)
MRC (MR/P501967/1)
Academy of Medical Sciences (SBF001\1016)
Medical Research Council (MC_PC_12012)
The work described in this publication was supported by funds from the Wellcome Trust, the Medical Research Council (MR/P501967/1), and the Academy of Medical Sciences (SBF001\1016).