Engineered Plant-Based Nanocellulose Hydrogel for Small Intestinal Organoid Growth.

hydrogels nanocellulose organoids rheology transcriptomic profile

Journal

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
ISSN: 2198-3844
Titre abrégé: Adv Sci (Weinh)
Pays: Germany
ID NLM: 101664569

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 08 06 2020
revised: 12 10 2020
entrez: 13 1 2021
pubmed: 14 1 2021
medline: 14 1 2021
Statut: epublish

Résumé

Organoids are three-dimensional self-renewing and organizing clusters of cells that recapitulate the behavior and functionality of developed organs. Referred to as "organs in a dish," organoids are invaluable biological models for disease modeling or drug screening. Currently, organoid culture commonly relies on an expensive and undefined tumor-derived reconstituted basal membrane which hinders its application in high-throughput screening, regenerative medicine, and diagnostics. Here, we introduce a novel engineered plant-based nanocellulose hydrogel is introduced as a well-defined and low-cost matrix that supports organoid growth. Gels containing 0.1% nanocellulose fibers (99.9% water) are ionically crosslinked and present mechanical properties similar to the standard animal-based matrix. The regulation of the osmotic pressure is performed by a salt-free strategy, offering conditions for cell survival and proliferation. Cellulose nanofibers are functionalized with fibronectin-derived adhesive sites to provide the required microenvironment for small intestinal organoid growth and budding. Comparative transcriptomic profiling reveals a good correlation with transcriptome-wide gene expression pattern between organoids cultured in both materials, while differences are observed in stem cells-specific marker genes. These hydrogels are tunable and can be combined with laminin-1 and supplemented with insulin-like growth factor (IGF-1) to optimize the culture conditions. Nanocellulose hydrogel emerges as a promising matrix for the growth of organoids.

Identifiants

pubmed: 33437574
doi: 10.1002/advs.202002135
pii: ADVS2236
pmc: PMC7788499
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2002135

Informations de copyright

© 2020 The Authors. Published by Wiley‐VCH GmbH.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

Références

Stem Cells Transl Med. 2017 Feb;6(2):622-633
pubmed: 28191779
Semin Cancer Biol. 2005 Oct;15(5):378-86
pubmed: 15975825
Nat Commun. 2019 Dec 11;10(1):5658
pubmed: 31827102
J Exp Med. 1977 Jan 1;145(1):204-20
pubmed: 830788
Nat Rev Genet. 2018 Nov;19(11):671-687
pubmed: 30228295
Nature. 2019 May;569(7754):66-72
pubmed: 31019299
Nature. 2016 Nov 24;539(7630):560-564
pubmed: 27851739
Bioinformatics. 2015 Jan 15;31(2):166-9
pubmed: 25260700
Biomacromolecules. 2007 Aug;8(8):2485-91
pubmed: 17630692
Acta Biomater. 2016 Oct 15;44:200-8
pubmed: 27545811
J Control Release. 2012 Dec 28;164(3):291-8
pubmed: 22776290
Am J Pathol. 2008 May;172(5):1441; author reply 1441-2
pubmed: 18403599
Nature. 2016 Feb 18;530(7590):340-3
pubmed: 26863187
Cell Stem Cell. 2017 Aug 3;21(2):274-283.e5
pubmed: 28736217
Cell Stem Cell. 2012 Oct 5;11(4):452-60
pubmed: 23040474
Cell. 2009 Mar 6;136(5):903-12
pubmed: 19269367
Cell. 2008 Feb 8;132(3):487-98
pubmed: 18267078
FASEB J. 2015 Jul;29(7):2828-42
pubmed: 25837582
Proteomics. 2010 May;10(9):1886-90
pubmed: 20162561
Curr Opin Neurobiol. 2012 Oct;22(5):768-77
pubmed: 22405989
Nature. 2019 May;569(7754):121-125
pubmed: 31019301
EMBO J. 2008 Nov 5;27(21):2829-38
pubmed: 18843297
Cell. 2016 Jun 16;165(7):1586-1597
pubmed: 27315476
Genome Biol. 2014;15(12):550
pubmed: 25516281
Adv Mater. 2018 Oct;30(43):e1801621
pubmed: 30203567
Nat Methods. 2010 Mar;7(3):168-9
pubmed: 20195247
Adv Mater. 2020 Jul;32(30):e1905366
pubmed: 32548863
Cell. 2015 May 7;161(4):933-45
pubmed: 25957691
Cell Rep. 2019 Feb 26;26(9):2509-2520.e4
pubmed: 30811997
EMBO J. 2012 Jun 12;31(14):3079-91
pubmed: 22692129
Cell Adh Migr. 2013 Jan-Feb;7(1):48-55
pubmed: 23263632
Adv Healthc Mater. 2020 Mar;9(6):e1901658
pubmed: 32090504
Science. 2014 Jul 18;345(6194):1247125
pubmed: 25035496
Dev Cell. 2016 Sep 26;38(6):590-600
pubmed: 27676432
Stem Cells Int. 2017;2017:7970385
pubmed: 28835755
Adv Healthc Mater. 2019 Oct;8(19):e1900979
pubmed: 31402634
Nature. 2007 Oct 25;449(7165):1003-7
pubmed: 17934449
Nat Cell Biol. 2017 Nov;19(11):1326-1335
pubmed: 29058719
Nat Methods. 2015 Apr;12(4):357-60
pubmed: 25751142
Stem Cell Reports. 2019 Feb 12;12(2):381-394
pubmed: 30612954
Biomacromolecules. 2003 Sep-Oct;4(5):1417-25
pubmed: 12959614
Nat Commun. 2019 Apr 3;10(1):1523
pubmed: 30944313

Auteurs

Rodrigo Curvello (R)

Bioresource Processing Research Institute of Australia (BioPRIA) Department of Chemical Engineering Monash University Clayton Victoria 3800 Australia.

Genevieve Kerr (G)

Department of Anatomy and Developmental Biology and Development and Stem Cells Program Monash Biomedicine Discovery Institute Clayton Victoria 3800 Australia.

Diana J Micati (DJ)

Department of Anatomy and Developmental Biology and Development and Stem Cells Program Monash Biomedicine Discovery Institute Clayton Victoria 3800 Australia.

Wing Hei Chan (WH)

Department of Anatomy and Developmental Biology and Development and Stem Cells Program Monash Biomedicine Discovery Institute Clayton Victoria 3800 Australia.

Vikram S Raghuwanshi (VS)

Bioresource Processing Research Institute of Australia (BioPRIA) Department of Chemical Engineering Monash University Clayton Victoria 3800 Australia.

Joseph Rosenbluh (J)

Department of Biochemistry and Molecular Biology Monash University Clayton Victoria 3800 Australia.

Helen E Abud (HE)

Department of Anatomy and Developmental Biology and Development and Stem Cells Program Monash Biomedicine Discovery Institute Clayton Victoria 3800 Australia.

Gil Garnier (G)

Bioresource Processing Research Institute of Australia (BioPRIA) Department of Chemical Engineering Monash University Clayton Victoria 3800 Australia.

Classifications MeSH