Evidence map›Paper›PMID 24034597›Full record

ArticleJournal of cellular and molecular medicine2013

Interplay between human microglia and neural stem/progenitor cells in an allogeneic co-culture model.

Jia Liu, Erik Hjorth, Mingqin Zhu, Cinzia Calzarossa, Eva-Britt Samuelsson, Marianne Schultzberg, Elisabet Åkesson

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

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  15. Caffeine Compromises Proliferation of Human Hippocampal Progenitor Cells.Frontiers in cell and developmental biology · 2020
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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

7 authors at 3 institutions in 2 countries.

Jia LiuDepartment of Neurobiology, Care Sciences & Society, Karolinska Institutet, Geriatric Clinic Res Lab, Stockholm, Sweden; Department of Neurology, First Hospital of Jilin University, Changchun, China.
Erik Hjorth
Mingqin Zhu
Cinzia Calzarossa
Eva-Britt Samuelsson
Marianne Schultzberg
Elisabet Åkesson
Karolinska Institutet · SEFirst Hospital of Jilin University · CNSwedish Foundation for Strategic Research · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experimental neural cell therapies, including donor neural stem/progenitor cells (NPCs) have been reported to offer beneficial effects on the recovery after an injury and to counteract inflammatory and degenerative processes in the central nervous system (CNS). The interplay between donor neural cells and the host CNS still to a large degree remains unclear, in particular in human allogeneic conditions. Here, we focused our studies on the interaction of human NPCs and microglia utilizing a co-culture model. In co-cultures, both NPCs and microglia showed increased survival and proliferation compared with mono-cultures. In the presence of microglia, a larger subpopulation of NPCs expressed the progenitor cell marker nestin, whereas a smaller group of NPCs expressed the neural markers polysialylated neural cell adhesion molecule, A2B5 and glial fibrillary acidic protein compared with NPC mono-cultures. Microglia thus hindered differentiation of NPCs. The presence of human NPCs increased microglial phagocytosis of latex beads. Furthermore, we observed that the expression of CD200 molecules on NPCs and the CD200 receptor protein on microglia was enhanced in co-cultures, whereas the release of transforming growth factor-β was increased suggesting anti-inflammatory features of the co-cultures. To conclude, the interplay between human allogeneic NPCs and microglia, significantly affected their respective proliferation and phenotype. Neural cell therapy including human donor NPCs may in addition to offering cell replacement, modulate host microglial phenotypes and functions to benefit neuroprotection and repair.

Indexed as

AllograftsAntigens, CDAntigens, SurfaceCell CommunicationCell DifferentiationCell ProliferationCells, CulturedCell SurvivalCoculture TechniquesHumansInterleukin-6MicrogliaNeural Stem CellsOrexin ReceptorsPhagocytosisPhenotypeAntigens, CDantigens, CD200Antigens, SurfaceCD200R1 protein, humanIL6 protein, humanInterleukin-6Orexin ReceptorsReceptors, Cell SurfaceTransforming Growth Factor beta1CD200human neural stem/progenitor cellsimmunomodulationM1/M2 phenotypemicrogliaphagocytosistransforming growth factor-β

Identifiers

PMID24034597
PMCPMC4117556
OpenAlexW2013078581

What OpenQuestion holds

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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.