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Updated: Oct 26, 2025

Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays
Published on: January 8, 2017
Direct Differentiation of Functional Neurons from Human Pluripotent Stem Cells (hPSCs)
Ruiqi Hu1, Xiaoting Zhu1, Nan Yang2
1Department of Neuroscience, Icahn School of Medicine at Mount Sinai, Black Family Stem Cell Institute, Friedman Brain Institute, New York, NY, USA.
Abstract:
Somatic cell nuclear transfer and in vitro induction of pluripotency in somatic cells by defined factors provided unambiguous evidence that the epigenetic state of terminally differentiated somatic cells is not static and can be reversed to a more primitive one. Inspired by these results, stem cell biologists have identified approaches to directly convert fibroblasts into induced neuronal (iN) cells, indicating that direct lineage conversions are possible between distantly related cell types. More recently, we took advantages of pro-neurogenic capacity of iN factors and developed methods to rapidly derive functionally mature neurons directly from human pluripotent stem cells (hPSCs) through a brief induction of defined transcription factors. In this chapter, we describe the detailed methods used to attain the direct conversion from hPSCs to glutamatergic and GABAergic iN cells.

