Evidence map›Paper›PMID 34722855›Full record

ArticleRegenerative engineering and translational medicine2021

Local delivery of FTY720 induces neutrophil activation through chemokine signaling in an oronasal fistula model.

A M Amanso, T C Turner, A Kamalakar, S A Ballestas, L A Hymel, J Randall, R Johnston, R A Arthur, N J Willett, E A Botchwey and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Regenerative engineering and translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
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

11 authors at 3 institutions in 1 country.

A M AmansoDepartment of Otolaryngology, Emory University School of Medicine, 2015 Uppergate Drive, Atlanta, GA 30322 USA.
T C TurnerCoulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA USA.
A KamalakarDepartment of Otolaryngology, Emory University School of Medicine, 2015 Uppergate Drive, Atlanta, GA 30322 USA.
S A BallestasDepartment of Otolaryngology, Emory University School of Medicine, 2015 Uppergate Drive, Atlanta, GA 30322 USA.
L A HymelCoulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA USA.
J RandallThe Emory Integrated Computational Core, Emory University School of Medicine, Atlanta, GA USA.
R JohnstonThe Emory Integrated Computational Core, Emory University School of Medicine, Atlanta, GA USA.
R A ArthurThe Emory Integrated Computational Core, Emory University School of Medicine, Atlanta, GA USA.
N J WillettDepartment of Orthopedics, Emory University School of Medicine, Atlanta, GA USA.
E A BotchweyCoulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA USA.
S L GoudyDepartment of Otolaryngology, Emory University School of Medicine, 2015 Uppergate Drive, Atlanta, GA 30322 USA.
Emory University · USGeorgia Institute of Technology · USThe Wallace H. Coulter Department of Biomedical Engineering · US

Funding

Research Training Program Plan on Cell and Tissue Engineering (CTEng)T32GM008433 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J · 1991 to 2021
$7.1M
An immunomodulatory approach to improve oral cavity wound healingR01DE028905 · NIDCR · EMORY UNIVERSITY · PI GOUDY, STEVEN L · 2020 to 2024
$2.7M
Immune Modulatory Nanofibers for Skeletal Muscle ReconstructionR56AR071708 · NIAMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI BOTCHWEY, EDWARD A. · 2017 to 2018
$789k
NIAMS NIH HHS R56 AR071708NIDCR NIH HHS R01 DE028905NIGMS NIH HHS T32 GM008433
6 · The paper itself

Abstract

purposeCleft palate repair surgeries lack a regenerative reconstructive option and, in many cases, develop complications including oronasal fistula (ONF). Our group has developed a novel murine phenocopy of ONF to study the oral cavity wound healing program. Using this model, our team previously identified that delivery of FTY720 on a nanofiber scaffold had a unique immunomodulatory effect directing macrophages and monocytes into a pro-regenerative state during ONF healing. Here, the objective of this study was to determine the effects of local biomaterial-based FTY720 delivery in the ONF model on the early bulk gene expression and neutrophil phenotypic response within the regenerating tissue.

methodsUsing a mouse model of ONF formation, a palate defect was created and was treated with FTY720 nanofiber scaffolds or (blank) vehicle control nanofibers. At 1 and 3 days post-implantation, ONF oral mucosal tissue from the defect region was collected for RNA sequencing analysis or flow cytometry. For the RNA-seq expression profiling, intracellular pathways were assessed using the KEGG Pathway database and Gene Ontology (GO) Terms enrichment interactive graph. To assess the effects of FTY720 on different neutrophil subpopulations, flow cytometry data was analyzed using pseudotime analysis based on Spanning-tree Progression Analysis of Density-normalized Events (SPADE).

resultsRNA sequencing analysis of palate mucosa injured tissue identified 669 genes that were differentially expressed (DE) during the first 3 days of ONF wound healing after local delivery of FTY720, including multiple genes in the sphingolipid signaling pathway. Evaluation of the DE genes at the KEGG Pathway database also identified the inflammatory immune response pathways (chemokine signaling, cytokine-cytokine receptor interaction, and leukocyte transendothelial migration), and the Gene Ontology enrichment analysis identified neutrophil chemotaxis and migration terms. SPADE dendrograms of CD11b

conclusionTreatment of oral mucosal defects using FTY720 scaffolds is a promising new immunotherapy to improve healing outcomes and reducing ONF formation during cleft palate surgical repair. Local delivery of FTY720 nanofiber scaffolds during ONF healing significantly shifted early gene transcription associated with immune cell recruitment and modulation of the immune microenvironment results in distinct neutrophil subpopulations in the oral mucosal defect tissue that provides a critical shift toward pro-regenerative immune signaling. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40883-021-00208-z.

Indexed as

FTY720NeutrophilOronasal fistulaWound healing

Identifiers

PMID34722855
PMCPMC8549964
OpenAlexW3163736106

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.