Evidence map›Paper›PMID 28276602›Full record

ArticleStem cells (Dayton, Ohio)2017

Multifactorial Experimental Design to Optimize the Anti-Inflammatory and Proangiogenic Potential of Mesenchymal Stem Cell Spheroids.

Kaitlin C Murphy, Jacklyn Whitehead, Patrick C Falahee, Dejie Zhou, Scott I Simon, J Kent Leach

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 102 citations in OpenAlex.

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4 more citing papers are in PubMed but not listed here.

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.

Kaitlin C MurphyDepartment of Biomedical Engineering, University of California Davis, Davis, California, USA.
Jacklyn WhiteheadDepartment of Biomedical Engineering, University of California Davis, Davis, California, USA.
Patrick C FalaheeDepartment of Biomedical Engineering, University of California Davis, Davis, California, USA.
Dejie ZhouDepartment of Biomedical Engineering, University of California Davis, Davis, California, USA.
Scott I SimonDepartment of Biomedical Engineering, University of California Davis, Davis, California, USA.
J Kent LeachDepartment of Biomedical Engineering, University of California Davis, Davis, California, USA.ORCID 0000-0002-1673-3335
University of California, Davis · US

Funding

Outside-in Mechanotransduced Inflammatory TargetsR01AI047294 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI SIMON, SCOTT IRWIN · 1999 to 2021
$7.0M
Biomaterial regulation of cell spheroids to synergistically enhance bone healingR01DE025475 · NIDCR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEACH, J. KENT · 2015 to 2019
$1.9M
Engineering the innate immune response to Staphaureus infectionR01AI129302 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEACH, J. KENT, SIMON, SCOTT IRWIN · 2017 to 2021
$1.9M
NIAID NIH HHS R01 AI047294NIAID NIH HHS R01 AI129302NIDCR NIH HHS R01 DE025475
6 · The paper itself

Abstract

Mesenchymal stem cell therapies promote wound healing by manipulating the local environment to enhance the function of host cells. Aggregation of mesenchymal stem cells (MSCs) into three-dimensional spheroids increases cell survival and augments their anti-inflammatory and proangiogenic potential, yet there is no consensus on the preferred conditions for maximizing spheroid function in this application. The objective of this study was to optimize conditions for forming MSC spheroids that simultaneously enhance their anti-inflammatory and proangiogenic nature. We applied a design of experiments (DOE) approach to determine the interaction between three input variables (number of cells per spheroid, oxygen tension, and inflammatory stimulus) on MSC spheroids by quantifying secretion of prostaglandin E

Indexed as

Neovascularization, PhysiologicAnti-Inflammatory AgentsCell PolarityCell SizeCellular MicroenvironmentColony-Forming Units AssayCulture Media, ConditionedHumansMacrophage ActivationMesenchymal Stem CellsNF-kappa BPhenotypeReproducibility of ResultsResearch DesignSignal TransductionSkin, ArtificialAnti-Inflammatory AgentsCulture Media, ConditionedNF-kappa BTumor Necrosis Factor-alphaDesign of experimentsInflammationMesenchymal stem cellProangiogenicProstaglandin E2

Identifiers

PMID28276602
PMCPMC5446296
OpenAlexW2592446816

What OpenQuestion holds

Textmetadata
LicenceTDM
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.