Evidence map›Paper›PMID 35917808›Full record

ArticleBiofabrication2022

Hybrid extracellular vesicles-liposome incorporated advanced bioink to deliver microRNA.

Kamil Elkhoury, Mo Chen, Polen Koçak, Eduardo Enciso-Martínez, Nicole Joy Bassous, Myung Chul Lee, Batzaya Byambaa, Zahra Rezaei, Yang Li, María Elizabeth Ubina López and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Biofabrication, 2022. 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
3.1field-weighted citation impact, top 8% 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, 39 citations in OpenAlex.

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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

19 authors at 4 institutions in 7 countries.

Kamil ElkhouryDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.ORCID 0000-0001-8160-9333
Mo ChenDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.
Polen KoçakDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.
Eduardo Enciso-MartínezDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.ORCID 0000-0003-4813-3251
Nicole Joy BassousDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.
Myung Chul LeeDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.
Batzaya Byambaa3D BioLabs, LLC, 700 Main St., Cambridge, MA 02138, United States of America.
Zahra RezaeiDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.
Yang LiDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.
María Elizabeth Ubina LópezDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.
Melvin GurianDepartment of Developmental BioEngineering, University of Twente, Enschede, Overijssel 7522 NB, The Netherlands.
Nebras SobahiDepartment of Electrical and Computer Engineering, King Abdulaziz University, Jeddah 21569, Saudi Arabia.
Mohammad Asif HussainDepartment of Electrical and Computer Engineering, King Abdulaziz University, Jeddah 21569, Saudi Arabia.
Laura Sanchez-GonzalezLIBio, Université de Lorraine, F-54000 Nancy, France.
Jeroen LeijtenDepartment of Developmental BioEngineering, University of Twente, Enschede, Overijssel 7522 NB, The Netherlands.
Shabir HassanDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.
Elmira Arab-TehranyLIBio, Université de Lorraine, F-54000 Nancy, France.
Jennifer Ellis WardDepartment of Medicine, Harvard Medical School, Brigham and Women's Hospital, Boston, MA 02115, United States of America.
Su Ryon ShinDivision of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, United States of America.ORCID 0000-0003-0864-6482
Brigham and Women's Hospital · USKing Abdulaziz University · SAUniversité de Lorraine · FRUniversity of Twente · NL

Funding

Suturable bioprinted vascularized muscle constructs for treatment of skeletal muscle lossR01AR077132 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SHIN, SU RYON, TAMAYOL, ALI · 2021 to 2025
$2.6M
Oxygen generating bioinks for 3D printed bone implantsR01AR074234 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SHIN, SU RYON · 2018 to 2022
$1.9M
Microengineered scaffolds carrying patient-specific cells and growth factors for treatment of volumetric muscle lossR01AR073822 · NIAMS · UNIVERSITY OF NEBRASKA LINCOLN · PI TAMAYOL, ALI · 2018 to 2022
$1.8M
Programmable multimaterial bioprinting of 3D vascularized tissue constructsR21EB026824 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI SHIN, SU RYON · 2018 to 2020
$685k
NIAMS NIH HHS R01 AR073822NIAMS NIH HHS R01 AR074234NIAMS NIH HHS R01 AR077132NIBIB NIH HHS R21 EB026824
6 · The paper itself

Abstract

In additive manufacturing, bioink formulations govern strategies to engineer 3D living tissues that mimic the complex architectures and functions of native tissues for successful tissue regeneration. Conventional 3D-printed tissues are limited in their ability to alter the fate of laden cells. Specifically, the efficient delivery of gene expression regulators (i.e. microRNAs (miRNAs)) to cells in bioprinted tissues has remained largely elusive. In this study, we explored the inclusion of extracellular vesicles (EVs), naturally occurring nanovesicles (NVs), into bioinks to resolve this challenge. EVs show excellent biocompatibility, rapid endocytosis, and low immunogenicity, which lead to the efficient delivery of miRNAs without measurable cytotoxicity. EVs were fused with liposomes to prolong and control their release by altering their physical interaction with the bioink. Hybrid EVs-liposome (hEL) NVs were embedded in gelatin-based hydrogels to create bioinks that could efficiently encapsulate and deliver miRNAs at the target site in a controlled and sustained manner. The regulation of cells' gene expression in a 3D bioprinted matrix was achieved using the hELs-laden bioink as a precursor for excellent shape fidelity and high cell viability constructs. Novel regulatory factors-loaded bioinks will expedite the translation of new bioprinting applications in the tissue engineering field.

Indexed as

BioprintingExtracellular VesiclesMicroRNAsHydrogelsLiposomesPrinting, Three-DimensionalTissue EngineeringTissue ScaffoldsHydrogelsLiposomesMicroRNAs3D bioprintingbioinkextracellular vesiclesliposomesmicroRNAstissue regeneration

Identifiers

PMID35917808
PMCPMC9594995
OpenAlexW4289519011

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.