Evidence map›Paper›PMID 29078295›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Intercellular mRNA trafficking via membrane nanotube-like extensions in mammalian cells.

Gal Haimovich, Christopher M Ecker, Margaret C Dunagin, Elliott Eggan, Arjun Raj, Jeffrey E Gerst, Robert H Singer

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
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

70 citing papers in PubMed, 121 citations in OpenAlex.

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  19. Intercellular mRNA transfer alters the human pluripotent stem cell state.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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10 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 2 countries.

Gal HaimovichDepartment of Molecular Genetics, Weizmann Institute of Science, Rehovot 7610001, Israel.
Christopher M EckerDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104.
Margaret C DunaginDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104.
Elliott EgganDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104.
Arjun RajDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104.
Jeffrey E GerstDepartment of Molecular Genetics, Weizmann Institute of Science, Rehovot 7610001, Israel; jeffrey.gerst@weizmann.ac.il robert.singer@einstein.yu.edu.
Robert H SingerDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461; jeffrey.gerst@weizmann.ac.il robert.singer@einstein.yu.edu.ORCID 0000-0002-6725-0093
University of Pennsylvania · USAlbert Einstein College of Medicine · USWeizmann Institute of Science · IL

Funding

Mechanism of MRNA Localization and Localized Translation in NeuronsR01NS083085 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Sulagna Das, Robert H Singer · 2013 to 2026
$9.0M
A Comprehensive Spatial Picture of Transcription in the NucleusDP2OD008514 · OD · UNIVERSITY OF PENNSYLVANIA · PI RAJ, ARJUN · 2011 to 2011
$2.4M
NIH HHS DP2 OD008514NINDS NIH HHS R01 NS083085
6 · The paper itself

Abstract

RNAs have been shown to undergo transfer between mammalian cells, although the mechanism behind this phenomenon and its overall importance to cell physiology is not well understood. Numerous publications have suggested that RNAs (microRNAs and incomplete mRNAs) undergo transfer via extracellular vesicles (e.g., exosomes). However, in contrast to a diffusion-based transfer mechanism, we find that full-length mRNAs undergo direct cell-cell transfer via cytoplasmic extensions characteristic of membrane nanotubes (mNTs), which connect donor and acceptor cells. By employing a simple coculture experimental model and using single-molecule imaging, we provide quantitative data showing that mRNAs are transferred between cells in contact. Examples of mRNAs that undergo transfer include those encoding GFP, mouse β-actin, and human Cyclin D1, BRCA1, MT2A, and HER2. We show that intercellular mRNA transfer occurs in all coculture models tested (e.g., between primary cells, immortalized cells, and in cocultures of immortalized human and murine cells). Rapid mRNA transfer is dependent upon actin but is independent of de novo protein synthesis and is modulated by stress conditions and gene-expression levels. Hence, this work supports the hypothesis that full-length mRNAs undergo transfer between cells through a refined structural connection. Importantly, unlike the transfer of miRNA or RNA fragments, this process of communication transfers genetic information that could potentially alter the acceptor cell proteome. This phenomenon may prove important for the proper development and functioning of tissues as well as for host-parasite or symbiotic interactions.

Indexed as

Cell CommunicationNanotubesActininActinsAnimalsCell LineCoculture TechniquesCyclin D1Erb-b2 Receptor Tyrosine KinasesExosomesFibroblastsGene Expression RegulationHost-Parasite InteractionsHumansMetallothioneinMiceActininActinsBRAP protein, humanCyclin D1ERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMetallothioneinMicroRNAsMT2A protein, humanProteomeRNA, MessengerUbiquitin-Protein Ligasesmembrane nanotubesMS2smFISHβ-actin mRNA

Identifiers

PMID29078295
PMCPMC5699038
OpenAlexW2766403075

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.