Publication:

Combinatorial programming of human neuronal progenitors using magnetically-guided stoichiometric mRNA delivery

Loading...
Thumbnail Image

Open/View Files

Date

2018

Published Version

Journal Title

Journal ISSN

Volume Title

Publisher

eLife Sciences Publications, Ltd
The Harvard community has made this article openly available. Please share how this access benefits you.

Research Projects

Organizational Units

Journal Issue

Citation

Azimi, Sayyed M, Steven D Sheridan, Mostafa Ghannad-Rezaie, Peter M Eimon, and Mehmet Fatih Yanik. 2018. “Combinatorial programming of human neuronal progenitors using magnetically-guided stoichiometric mRNA delivery.” eLife 7 (1): e31922. doi:10.7554/eLife.31922. http://dx.doi.org/10.7554/eLife.31922.

Abstract

Identification of optimal transcription factor expression patterns to direct cellular differentiation along a desired pathway presents significant challenges. We demonstrate massively combinatorial screening of temporally-varying mRNA transcription factors to direct differentiation of neural progenitor cells using a dynamically-reconfigurable magnetically-guided spotting technology for localizing mRNA, enabling experiments on millimetre size spots. In addition, we present a time-interleaved delivery method that dramatically reduces fluctuations in the delivered transcription factor copy numbers per cell. We screened combinatorial and temporal delivery of a pool of midbrain-specific transcription factors to augment the generation of dopaminergic neurons. We show that the combinatorial delivery of LMX1A, FOXA2 and PITX3 is highly effective in generating dopaminergic neurons from midbrain progenitors. We show that LMX1A significantly increases TH-expression levels when delivered to neural progenitor cells either during proliferation or after induction of neural differentiation, while FOXA2 and PITX3 increase expression only when delivered prior to induction, demonstrating temporal dependence of factor addition.

Description

Research Data

Keywords

neuron, stem cell, reprogramming, high-throughput, screening, transcription factors, neuron type, dopaminergic neurons, neuronal differentiation, Human

Terms of Use

This article is made available under the terms and conditions applicable to Other Posted Material (LAA), as set forth at Terms of Service

Endorsement

Review

Supplemented By

Related Stories