Evidence map›Paper›PMID 34027099›Full record

ArticleBioengineering & translational medicine2021

Mesenchymal stem cell-inspired microgel scaffolds to control macrophage polarization.

Alexander S Caldwell, Varsha V Rao, Alyxandra C Golden, Daniel J Bell, Joseph C Grim, Kristi S Anseth

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. 3D Culture of MSCs for Clinical Application.Bioengineering (Basel, Switzerland) · 2024
    Review
  7. Article
  8. Granular Hydrogels for Harnessing the Immune Response.Advanced healthcare materials · 2024
    Review
  9. Targeted liposomes for macrophages-mediated pulmonary fibrosis therapy.Drug delivery and translational research · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Void Volume Fraction of Granular Scaffolds.Small (Weinheim an der Bergstrasse, Germany) · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Macrophage-targeted delivery of siRNA to silenceBioengineering & translational medicine · 2022
    Article
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Alexander S CaldwellDepartment of Chemical and Biological Engineering University of Colorado Boulder Colorado USA.ORCID https://orcid.org/0000-0002-5790-118X
Varsha V RaoDepartment of Chemical and Biological Engineering University of Colorado Boulder Colorado USA.
Alyxandra C GoldenDepartment of Chemical and Biological Engineering University of Colorado Boulder Colorado USA.
Daniel J BellDepartment of Chemical and Biological Engineering University of Colorado Boulder Colorado USA.
Joseph C GrimDepartment of Chemical and Biological Engineering University of Colorado Boulder Colorado USA.
Kristi S AnsethDepartment of Chemical and Biological Engineering University of Colorado Boulder Colorado USA.ORCID https://orcid.org/0000-0002-5725-5691
University of Colorado Boulder · US

Funding

POSTGRADUATE TRAINING IN CARDIOVASCULAR RESEARCHT32HL007822 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI BUTTRICK, PETER N., LEINWAND, LESLIE ANNE · 1996 to 2023
$6.2M
Osteogenic Hydrogel Niches to Promote hMSC Migration and DifferentiationR01DE016523 · NIDCR · UNIVERSITY OF COLORADO AT BOULDER · PI ANSETH, KRISTI S. · 2005 to 2023
$6.2M
NHLBI NIH HHS T32 HL007822NIDCR NIH HHS R01 DE016523
6 · The paper itself

Abstract

There is a desire in regenerative medicine to create biofunctional materials that can control and direct cell function in a precise manner. One particular stem cell of interest, human mesenchymal stem cells (hMSCs), can function as regulators of the immunogenic response and aid in tissue regeneration and wound repair. Here, a porous hydrogel scaffold assembled from microgel subunits was used to recapitulate part of this immunomodulatory behavior. The scaffolds were used to culture a macrophage cell line, while cytokines were delivered exogenously to polarize the macrophages to either a pro-inflammatory (M1) or alternatively activated (M2a) phenotypes. Using a cytokine array, interleukin 10 (IL-10) was identified as one key anti-inflammatory factor secreted by hMSCs in pro-inflammatory conditions; it was elevated (125 ± 25 pg/ml) in pro-inflammatory conditions compared to standard medium (6 ± 10 pg/ml). The ability of hMSC laden scaffolds to reverse the M1 phenotype was then examined, even in the presence of exogenous pro-inflammatory cytokines. Co-culture of M1 and M2 macrophages with hMSCs reduced the secretion of TNFα, a pro-inflammatory cytokine even in the presence of pro-inflammatory stimulatory factors. Next, IL-10 was supplemented in the medium or tethered directly to the microgel subunits; both methods limited the secretion of pro-inflammatory cytokines of encapsulated macrophages even in pro-inflammatory conditions. Cumulatively, these results reveal the potential of biofunctional microgel-based scaffolds as acellular therapies to present anti-inflammatory cytokines and control the immunogenic cascade.

Indexed as

hydrogelIL‐10immunomodulatorymacrophagemicrogelMSC

Identifiers

PMID34027099
PMCPMC8126823
OpenAlexW3134045160

What OpenQuestion holds

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LicenceCC BY
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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.