Evidence map›Paper›PMID 40575147›Full record

ArticleBiology methods & protocols2025

Neuro293: A REST-knockout HEK-293 cell line enables the expression of neuron-restricted genes for the high-throughput testing of human neurobiology and the biochemistry of neuronal proteins.

Joshua T Moses, Fahad B Shah, Nicholas M McVay, Dylan E Capes, Christopher C Bosse-Joseph, Jocelyn Salazar, Victoria K Slone, John E Eberth, Jonathan Satin, Andrew N Stewart

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Article in Biology methods & protocols, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Joshua T MosesDepartment of Physiology, University of Kentucky, Lexington, KY 40536, United States.
Fahad B ShahSpinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, KY 40536, United States.
Nicholas M McVayDepartment of Physiology, University of Kentucky, Lexington, KY 40536, United States.ORCID https://orcid.org/0000-0001-9719-2675
Dylan E CapesSpinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, KY 40536, United States.
Christopher C Bosse-JosephSpinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, KY 40536, United States.
Jocelyn SalazarSpinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, KY 40536, United States.
Victoria K SloneSpinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, KY 40536, United States.
John E EberthDepartment of Physiology, University of Kentucky, Lexington, KY 40536, United States.
Jonathan SatinDepartment of Physiology, University of Kentucky, Lexington, KY 40536, United States.
Andrew N StewartSpinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, KY 40536, United States.ORCID https://orcid.org/0000-0003-0607-6578

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient interrogation of neurobiology remains bottlenecked by obtaining mature neurons. Immortalized cell lines still require lengthy differentiation periods to obtain neuron-like cells, which may not efficiently differentiate and are challenging to transfect with plasmids relative to other cell lines such as HEK-293's. To overcome challenges with limited access to cells that express mature neuronal proteins, we knocked out the RE1-silencing transcription factor (REST) from HEK-293's to create a novel neuron-like cell, which we name Neuro293. RNA-sequencing and bioinformatics analyses revealed a significant upregulation of genes associated with neurobiology and membrane excitability including pre-/post-synaptic proteins, voltage gated ion channels, neuron-cytoskeleton, as well as neurotransmitter synthesis, packaging, and release. Western blot validated the upregulation of Synapsin-1 (Syn1) and Snap-25 as two neuron-restricted proteins, as well as the potassium channel Kv1.2. Immunocytochemistry against Neurofilament 200 kd revealed a significant upregulation and accumulation in singular processes extending from Neuro293's cell body. Similarly, while Syn1 increased in the cell body, Syn1 protein accumulated at the ends of processes extruding from Neuro293's. Neuro293's express reporter-genes through the Syn1 promoter after infection with adeno-associated viruses (AAV). However, transient transfection with AAV2 plasmids led to leaky expression through promoter-independent mechanisms. Despite an upregulation of many voltage-gated ion channels, Neuro293's do not possess excitable membranes. Collectively, REST-knockout in HEK-293's induces a quickly dividing and easily transfectable cell line that expresses neuron-restricted and mature neuronal proteins which can be used for high-throughput biochemical interrogation, however, without further modifications neither HEK-293's or Neuro293's exhibit properties of excitable membranes.

Indexed as

high-throughput testingmature neuronal proteinsneuronal differentiationstable cell line

Identifiers

PMID40575147
PMCPMC12202048

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