Evidence map›Paper›PMID 26758208›Full record

ArticleBMC cell biology2016

The role of neural connexins in HeLa cell mobility and intercellular communication through tunneling tubes.

Lina Rimkutė, Vaidas Jotautis, Alina Marandykina, Renata Sveikatienė, Ieva Antanavičiūtė, Vytenis Arvydas Skeberdis

Open access · goldAbstract read
In one paragraph

Article in BMC cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

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  2. Microbiology spectrum · 2022
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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

6 authors at 1 institution in 1 country.

Lina RimkutėInstitute of Cardiology, Lithuanian University of Health Sciences, 17 Sukilėlių Ave., 50009, Kaunas, Lithuania. lina.rimkute@lsmuni.lt.
Vaidas JotautisInstitute of Cardiology, Lithuanian University of Health Sciences, 17 Sukilėlių Ave., 50009, Kaunas, Lithuania. vaidas.jotautis@lsmuni.lt.
Alina MarandykinaInstitute of Cardiology, Lithuanian University of Health Sciences, 17 Sukilėlių Ave., 50009, Kaunas, Lithuania. alina.marandykina@fc.lsmuni.lt.
Renata SveikatienėInstitute of Cardiology, Lithuanian University of Health Sciences, 17 Sukilėlių Ave., 50009, Kaunas, Lithuania. renata.sveikatiene@lsmuni.lt.
Ieva AntanavičiūtėInstitute of Cardiology, Lithuanian University of Health Sciences, 17 Sukilėlių Ave., 50009, Kaunas, Lithuania. ieva.antanaviciute@lsmuni.lt.
Vytenis Arvydas SkeberdisInstitute of Cardiology, Lithuanian University of Health Sciences, 17 Sukilėlių Ave., 50009, Kaunas, Lithuania. arvydas.skeberdis@lsmuni.lt.
Lithuanian University of Health Sciences · LT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMembranous tunneling tubes (TTs) are a recently discovered new form of communication between remote cells allowing their electrical synchronization, migration, and transfer of cellular materials. TTs have been identified in the brain and share similarities with neuronal processes. TTs can be open-ended, close-ended or contain functional gap junctions at the membrane interface. Gap junctions are formed of two unapposed hemichannels composed of six connexin (Cx) subunits. There are evidences that Cxs also play channel-independent role in cell adhesion, migration, division, differentiation, formation of neuronal networks and tumorigenicity. These properties of Cxs and TTs may synergetically determine the cellular and intercellular processes. Therefore, we examined the impact of Cxs expressed in the nervous system (Cx36, Cx40, Cx43, Cx45, and Cx47) on: 1) cell mobility; 2) formation and properties of TTs; and 3) transfer of siRNA between remote cells through TTs.

resultsWe have identified two types of TTs between HeLa cells: F-actin rich only and containing F-actin and α-tubulin. The morphology of TTs was not influenced by expression of examined connexins; however, Cx36-EGFP-expressing cells formed more TTs while cells expressing Cx43-EGFP, Cx45, and Cx47 formed fewer TTs between each other compared with wt and Cx40-CFP-expressing cells. Also, Cx36-EGFP and Cx40-CFP-expressing HeLa cells were more mobile compared with wt and other Cxs-expressing cells. TTs containing Cx40-CFP, Cx43-EGFP, or Cx47 gap junctions were capable of transmitting double-stranded small interfering RNA; however, Cx36-EGFP and Cx45 were not permeable to it. In addition, we show that Cx43-EGFP-expressing HeLa cells and laryngeal squamous cell carcinoma cells can couple to the mesenchymal stem cells through TTs.

conclusionsDifferent Cxs may modulate the mobility of cells and formation of TTs in an opposite manner; siRNA transfer through the GJ-containing TTs is Cx isoform-dependent.

Indexed as

Cell CommunicationCell MovementConnexinsGap JunctionsHeLa CellsHumansNerve TissueConnexins

Identifiers

PMID26758208
PMCPMC4710989
OpenAlexW2234329742

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.