Evidence map›Paper›PMID 38345178›Full record

ArticleAdvanced healthcare materials2024

Neutrophil Granulopoiesis Optimized Through Ex Vivo Expansion of Hematopoietic Progenitors in Engineered 3D Gelatin Methacrylate Hydrogels.

Evan Cirves, Alex Vargas, Erika E Wheeler, Jonathan Kent Leach, Scott I Simon, Tomas Gonzalez-Fernandez

Open access · bronzeAbstract read
In one paragraph

Article in Advanced healthcare materials, 2024. 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
1.4field-weighted citation impact, top 20% 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, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

6 authors at 2 institutions in 1 country.

Evan CirvesDepartment of Biomedical Engineering, University of California at Davis, 451 East Health Sciences Drive, 2303 GBSF, Davis, CA, 95616, USA.
Alex VargasDepartment of Biomedical Engineering, University of California at Davis, 451 East Health Sciences Drive, 2303 GBSF, Davis, CA, 95616, USA.
Erika E WheelerDepartment of Biomedical Engineering, University of California at Davis, 451 East Health Sciences Drive, 2303 GBSF, Davis, CA, 95616, USA.
Jonathan Kent LeachDepartment of Orthopaedic Surgery, UC Davis Health, 4860 Y Street, Suite 3800, Sacramento, CA, 95817, USA.
Scott I SimonDepartment of Biomedical Engineering and Dermatology, University of California at Davis, Davis, CA, 95616, USA.
Tomas Gonzalez-FernandezDepartment of Bioengineering, Lehigh University, 124 E Morton Street, Health Science and Technology Building, Bethlehem, PA, 18015, USA.ORCID 0000-0002-4646-0905
University of California, Davis · USLehigh University · US

Funding

An Integrated In Vitro 3D Model of Human Bone Marrow and Peripheral InfectionR01EB030410 · NIBIB · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GEORGE, STEVEN CARL · 2021 to 2024
$2.6M
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
Division of Intramural Research, National Institute of Allergy and Infectious Diseases NIH AI129302NIAID NIH HHS R01 AI129302NIBIB NIH HHS R01 EB030410P.C. Rossin College of Engineering & Applied Science at Lehigh University.
6 · The paper itself

Abstract

Neutrophils are the first line of defense of the innate immune system. In response to methicillin-resistant Staphylococcus aureus infection in the skin, hematopoietic stem, and progenitor cells (HSPCs) traffic to wounds and undergo extramedullary granulopoiesis, producing neutrophils necessary to resolve the infection. This prompted the engineering of a gelatin methacrylate (GelMA) hydrogel that encapsulates HSPCs within a matrix amenable to subcutaneous delivery. The authors study the influence of hydrogel mechanical properties to produce an artificial niche for granulocyte-monocyte progenitors (GMPs) to efficiently expand into functional neutrophils that can populate infected tissue. Lin-cKIT+ HSPCs, harvested from fluorescent neutrophil reporter mice, are encapsulated in GelMA hydrogels of varying polymer concentration and UV-crosslinked to produce HSPC-laden gels of specific stiffness and mesh sizes. Softer 5% GelMA gels yield the most viable progenitors and effective cell-matrix interactions. Compared to suspension culture, 5% GelMA results in a twofold expansion of mature neutrophils that retain antimicrobial functions including degranulation, phagocytosis, and ROS production. When implanted dermally in C57BL/6J mice, luciferase-expressing neutrophils expanded in GelMA hydrogels are visualized at the site of implantation for over 5 days. They demonstrate the potential of GelMA hydrogels for delivering HSPCs directly to the site of skin infection to promote local granulopoiesis.

Indexed as

GelatinHematopoietic Stem CellsHydrogelsMethacrylatesMice, Inbred C57BLNeutrophilsAnimalsMiceGelatinHydrogelsMethacrylatesextramedullary granulopoiesisgelatin methacrylate (GelMA)hematopoietic stem and progenitor cells (HSPCs)neutrophils

Identifiers

PMID38345178
PMCPMC11144100
OpenAlexW4391744357

What Socratic 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 Socratic graph.