Evidence map›Paper›PMID 31032349›Full record

ArticleBioMed research international2019

Differentiation of Bone Marrow Mesenchymal Stem Cells into Neural Lineage Cells Induced by bFGF-Chitosan Controlled Release System.

Manli Li, Wen Zhao, Yudan Gao, Peng Hao, Junkui Shang, Hongmei Duan, Zhaoyang Yang, Xiaoguang Li

Abstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Cell-Based Therapies for Glaucoma.Translational vision science & technology · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. 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

8 authors.

Manli LiBeijing Key Laboratory for Biomaterials and Neural Regeneration, School of Biological Science and Medical Engineering, Beihang University, 100083 Beijing, China.ORCID 0000-0002-1839-7777
Wen ZhaoDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, 100069 Beijing, China.ORCID 0000-0003-4566-5914
Yudan GaoDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, 100069 Beijing, China.ORCID 0000-0003-2655-1305
Peng HaoDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, 100069 Beijing, China.ORCID 0000-0001-8532-8360
Junkui ShangDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, 100069 Beijing, China.ORCID 0000-0001-5160-315X
Hongmei DuanDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, 100069 Beijing, China.ORCID 0000-0003-2261-2182
Zhaoyang YangDepartment of Neurobiology, School of Basic Medical Sciences, Capital Medical University, 100069 Beijing, China.ORCID 0000-0001-8313-6998
Xiaoguang LiBeijing Key Laboratory for Biomaterials and Neural Regeneration, School of Biological Science and Medical Engineering, Beihang University, 100083 Beijing, China.ORCID 0000-0002-2228-7490

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone marrow mesenchymal stem cells undergo differentiation to different lineages with different efficiencies when induced by different factors. We added a bFGF-chitosan controlled release system (bFGF-CCRS) as an inducer into conditioned medium to facilitate the oriented differentiation of BMSCs into neural lineage cells (eventually mature neurons); furthermore, we synchronized BMSCs to the G0/G1 phase via serum starvation to observe the effect of the inducer on the differentiation direction and efficiency. The nonsynchronized group, chitosan alone (not loaded with bFGF) group, soluble bFGF group, and conditioned medium group served as controls, and we observed the dynamic process of differentiation of BMSCs into neural lineage cells at different time points after the beginning of coculture. We analyzed the binding patterns of bFGF and chitosan and assayed the expression differences of key factors (FGFR1, ERK, and c-fos) and molecular switches (BTG2) that regulate the transformation from cell proliferation to differentiation. We also investigated the potential molecular mechanism of BMSC differentiation into neural lineage cells at a high percentage when induced by bFGF-CCRS.

Indexed as

AnimalsBone Marrow CellsCell DifferentiationCell LineageCell ProliferationChitosanFibroblast Growth Factor 2Gene Expression Regulation, DevelopmentalImmediate-Early ProteinsMesenchymal Stem CellsMitogen-Activated Protein Kinase 3Neural Stem CellsNeuronsProto-Oncogene Proteins c-fosRatsReceptor, Fibroblast Growth Factor, Type 1BTG2 protein, ratChitosanFibroblast Growth Factor 2Immediate-Early ProteinsMitogen-Activated Protein Kinase 3Proto-Oncogene Proteins c-fosReceptor, Fibroblast Growth Factor, Type 1Tumor Suppressor Proteins

Identifiers

PMID31032349
PMCPMC6457308

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.