Evidence map›Paper›PMID 40622529›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

In Vitro Culture of Primary Mouse Neurons to Study Neuronal Infection.

Guorong Sun, Abel Viejo-Borbolla

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Guorong SunInstitute of Virology, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0001-7549-7304
Abel Viejo-BorbollaInstitute of Virology, Hannover Medical School, Hannover, Germany. viejo-borbolla.abel@mh-hannover.de.ORCID https://orcid.org/0000-0001-6395-4010

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many human viral pathogens, such as the widely prevalent herpes simplex virus (HSV), exhibit neurotropism. The recurring latency and reactivation of HSV throughout a lifelong infection period make it a fascinating subject for study. However, investigating virus neurotropism and interactions with the nervous system requires accessible models. This chapter offers a detailed account of various in vitro models employing primary mouse neuronal cultures, encompassing ganglia explants and dissociated neurons from superior cervical ganglia, trigeminal ganglia, and dorsal root ganglia. These models include two-dimensional (2D) and 3D cultures, as well as microfluidic chambers (MFCs) capable of isolating neurites and neuronal somata. These setups enable the study of different infection pathways and processes, including infection routes (i.e., through neurite ends or neuronal somata) as well as virus transport within neurites. Additionally, they can also be useful for addressing the interaction between pathogens and neuronal cells, such as the regulation of neuroelectrophysiological activity and neurite outgrowth. Furthermore, these protocols could be easily adapted for isolating and culturing neurons from the central nervous system. Overall, this chapter provides a versatile toolkit for obtaining large amounts of mouse primary neurons, which are essential for studies requiring neuronal models in the field of life sciences.

Indexed as

Cell Culture TechniquesNeuronsPrimary Cell CultureAnimalsCells, CulturedGanglia, SpinalMiceNeuritesTrigeminal Ganglion3D cultureDorsal root gangliaGanglion explantMicrofluidic chamberNeurite outgrowthNeuronal infectionSuperior cervical gangliaTrigeminal ganglia

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.