Evidence map›Paper›PMID 35132159›Full record

ArticleScientific reports2022

Complement C5aR/LPS-induced BDNF and NGF modulation in human dental pulp stem cells.

Muhammad Irfan, Ji Hyun Kim, Robert E Druzinsky, Sriram Ravindran, Seung Chung

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  9. CaFrontiers in cell and developmental biology · 2025
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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

5 authors at 1 institution in 1 country.

Muhammad IrfanDepartment of Oral Biology, College of Dentistry, University of Illinois Chicago, 801 S. Paulina St, Chicago, IL, 60612, USA.
Ji Hyun KimDepartment of Oral Biology, College of Dentistry, University of Illinois Chicago, 801 S. Paulina St, Chicago, IL, 60612, USA.
Robert E DruzinskyDepartment of Oral Biology, College of Dentistry, University of Illinois Chicago, 801 S. Paulina St, Chicago, IL, 60612, USA.
Sriram RavindranDepartment of Oral Biology, College of Dentistry, University of Illinois Chicago, 801 S. Paulina St, Chicago, IL, 60612, USA.
Seung ChungDepartment of Oral Biology, College of Dentistry, University of Illinois Chicago, 801 S. Paulina St, Chicago, IL, 60612, USA. chungsh@uic.edu.
University of Illinois Chicago · US

Funding

Role of complement receptor C5L2 in reparative dentinogenesisR01DE029816 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHUNG, SEUNG · 2022 to 2025
$1.9M
Role of complement receptor C5L2 in reparative dentinogenesisR56DE029816 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHUNG, SEUNG · 2020 to 2020
$380k
Pulp fibroblast-mediated inferior alveolar nerve regenerationR03DE028637 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHUNG, SEUNG · 2020 to 2021
$320k
NIDCR NIH HHS R01 DE029816NIDCR NIH HHS R03 DE028637NIDCR NIH HHS R56 DE029816
6 · The paper itself

Abstract

Stem cells with the ability to differentiate into a variety of cells and secrete nerve regeneration factors have become an emerging option in nerve regeneration. Dental pulp stem cells (DPSCs) appear to be a good candidate for nerve regeneration given their accessibility, neural crest origin, and neural repair qualities. We have recently demonstrated that the complement C5a system, which is an important mediator of inflammation and tissue regeneration, is activated by lipoteichoic acid-treated pulp fibroblasts, and governs the production of brain-derived nerve growth factor (BDNF). This BDNF secretion promotes neurite outgrowth towards the injury site. Here, we extend our observation to DPSCs and compare their neurogenic ability to bone marrow-derived mesenchymal stem cells (BM-MSCs) under inflammatory stimulation. Our ELISA and immunostaining data demonstrate that blocking the C5a receptor (C5aR) reduced BDNF production in DPSCs, while treatment with C5aR agonist increased the BDNF expression, which suggests that C5aR has a positive regulatory role in the BDNF modulation of DPSCs. Inflammation induced by lipopolysaccharide (LPS) treatment potentiated this effect and is C5aR dependent. Most important, DPSCs produced significantly higher levels of C5aR-mediated BDNF compared to BM-MSCs. Taken together, our data reveal novel roles for C5aR and inflammation in modulation of BDNF and NGF in DPSCs.

Indexed as

Brain-Derived Neurotrophic FactorDental PulpHumansLipopolysaccharidesMesenchymal Stem CellsNerve Growth FactorNerve RegenerationReceptor, Anaphylatoxin C5aStem CellsBrain-Derived Neurotrophic FactorC5AR1 protein, humanLipopolysaccharidesNerve Growth FactorReceptor, Anaphylatoxin C5a

Identifiers

PMID35132159
PMCPMC8821590
OpenAlexW4210891950

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.