Evidence map›Paper›PMID 38457904›Full record

ArticleBiomaterials advances2024

In vitro development and optimization of cell-laden injectable bioprinted gelatin methacryloyl (GelMA) microgels mineralized on the nanoscale.

Mauricio Gonçalves da Costa Sousa, Gabriela de Souza Balbinot, Ramesh Subbiah, Rahul Madathiparambil Visalakshan, Anthony Tahayeri, Maria Elisa Lima Verde, Avathamsa Athirasala, Genevieve Romanowicz, Robert E Guldberg, Luiz E Bertassoni

Open access · greenAbstract read
In one paragraph

Article in Biomaterials advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Rethinking osteocyte modelsFrontiers in bioengineering and biotechnology · 2026
    Review
  5. Article
4 · The record

Corrections and comments

  • Update of
    2023
5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Mauricio Gonçalves da Costa SousaKnight Cancer Precision Biofabrication Hub, Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health & Science University, United States of America; Department of Oral Rehabilitation and Biosciences, School of Dentistry, Oregon Health & Science University, United States of America.
Gabriela de Souza BalbinotUniversidade Federal do Rio Grande do Sul - UFRGS, School of Dentistry, Dental Materials Department, Porto Alegre, RS, Brazil.
Ramesh SubbiahKnight Cancer Precision Biofabrication Hub, Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health & Science University, United States of America; Department of Oral Rehabilitation and Biosciences, School of Dentistry, Oregon Health & Science University, United States of America.
Rahul Madathiparambil VisalakshanKnight Cancer Precision Biofabrication Hub, Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health & Science University, United States of America; Department of Oral Rehabilitation and Biosciences, School of Dentistry, Oregon Health & Science University, United States of America.
Anthony TahayeriKnight Cancer Precision Biofabrication Hub, Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health & Science University, United States of America; Department of Oral Rehabilitation and Biosciences, School of Dentistry, Oregon Health & Science University, United States of America.
Maria Elisa Lima VerdeKnight Cancer Precision Biofabrication Hub, Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health & Science University, United States of America; Department of Oral Rehabilitation and Biosciences, School of Dentistry, Oregon Health & Science University, United States of America.
Avathamsa AthirasalaKnight Cancer Precision Biofabrication Hub, Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health & Science University, United States of America; Department of Oral Rehabilitation and Biosciences, School of Dentistry, Oregon Health & Science University, United States of America.
Genevieve RomanowiczKnight Campus for Accelerating Scientific Impact, University of Oregon, United States of America.
Robert E GuldbergKnight Campus for Accelerating Scientific Impact, University of Oregon, United States of America.
Luiz E BertassoniKnight Cancer Precision Biofabrication Hub, Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health & Science University, United States of America; Division of Oncological Sciences, Knight Cancer Institute, Oregon Health & Science University, United States of America; Center for Regenerative Medicine, School of Medicine, Oregon Health & Science University, United States of America; Department of Biomedical Engineering, School of Medicine Oregon Health & Science University, United States of America; Department of Oral Rehabilitation and Biosciences, School of Dentistry, Oregon Health & Science University, United States of America. Electronic address: bertasso@ohsu.edu.
Oregon Health & Science University · USUniversity of Oregon · USUniversidade Federal do Rio Grande do Sul · BR

Funding

Microengineering vascularized and innervated bone-like scaffolds as an alternative to autologous bone graftsR01DE029553 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI BERTASSONI, LUIZ EDUARDO · 2021 to 2025
$3.0M
Microengineering the Dental Pulp Vascular Microenvironment_Diversity SupplementR01DE026170 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI BERTASSONI, LUIZ EDUARDO · 2016 to 2020
$2.5M
PORT (Portland Oral health Research Training)T90DE030859 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI WU, HUI · 2021 to 2025
$2.1M
PORT (Portland Oral health Research Training)R90DE031533 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI WU, HUI · 2021 to 2025
$821k
Bone-like organoids to understand factors controlling local bone immune response and regenerationK99DE033689 · NIDCR · UNIVERSITY OF OREGON · PI ROMANOWICZ, GENEVIEVE ELIZABETH · 2024 to 2025
$444k
An organ-on-a-chip model system to study prostate cancer metastasis into vascularized boneR21CA263860 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI BERTASSONI, LUIZ EDUARDO, MORAN, AMY E · 2022 to 2023
$392k
NCI NIH HHS R21 CA263860NIDCR NIH HHS R01 DE026170NIDCR NIH HHS R01 DE029553NIDCR NIH HHS R90 DE031533NIDCR NIH HHS T90 DE030859
6 · The paper itself

Abstract

Bone defects may occur in different sizes and shapes due to trauma, infections, and cancer resection. Autografts are still considered the primary treatment choice for bone regeneration. However, they are hard to source and often create donor-site morbidity. Injectable microgels have attracted much attention in tissue engineering and regenerative medicine due to their ability to replace inert implants with a minimally invasive delivery. Here, we developed novel cell-laden bioprinted gelatin methacrylate (GelMA) injectable microgels, with controllable shapes and sizes that can be controllably mineralized on the nanoscale, while stimulating the response of cells embedded within the matrix. The injectable microgels were mineralized using a calcium and phosphate-rich medium that resulted in nanoscale crystalline hydroxyapatite deposition and increased stiffness within the crosslinked matrix of bioprinted GelMA microparticles. Next, we studied the effect of mineralization in osteocytes, a key bone homeostasis regulator. Viability stains showed that osteocytes were maintained at 98 % viability after mineralization with elevated expression of sclerostin in mineralized compared to non-mineralized microgels, showing that mineralization can effectively enhances osteocyte maturation. Based on our findings, bioprinted mineralized GelMA microgels appear to be an efficient material to approximate the bone microarchitecture and composition with desirable control of sample injectability and polymerization. These bone-like bioprinted mineralized biomaterials are exciting platforms for potential minimally invasive translational methods in bone regenerative therapies.

Indexed as

GelatinMicrogelsBiocompatible MaterialsMethacrylatesBiocompatible MaterialsGelatingelatin methacryloylMethacrylatesMicrogelsBioprintingBone tissue engineeringGelMAMicrogelsMineralizationOsteocytesSclerostin

Identifiers

PMID38457904
PMCPMC10997158
OpenAlexW4392346871

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.