In vitro interaction of human Wharton's jelly mesenchymal stem cells with biomimetic 3D scaffold.


Journal

Journal of biomedical materials research. Part A
ISSN: 1552-4965
Titre abrégé: J Biomed Mater Res A
Pays: United States
ID NLM: 101234237

Informations de publication

Date de publication:
06 2019
Historique:
received: 02 11 2018
revised: 24 12 2018
accepted: 03 01 2019
pubmed: 13 1 2019
medline: 15 7 2020
entrez: 13 1 2019
Statut: ppublish

Résumé

Study of cell-biomaterial interaction is a crucial aspect of bone tissue engineering to find a state-of-the-art functional substitute. In present study, the Wharton's jelly mesenchymal stem cells (hWJ-MSCs) behavior on three-dimensional biomimetic nano-hydroxyapatite/chitosan/gelatin (nHA/CS/Gel) scaffolds was investigated. The outcome was assessed by histological, biochemical and morphological tests. Results indicated that hWJ-MSCs attached onto the scaffold surface through membrane filopodia, uniformly spread throughout the contacting surface. It only took 3 days for the seeded cells to appear deep inside the scaffold, reflecting proper hWJ-MSCs adhesion and migration, evidenced by both scanning electron microscope and hematoxilin and eosin assessments. Additionally, the present fabricated nHA/CS/Gel scaffold proved to be non-toxic as it supported cell proliferation measured by 3-(4,5-dimethylthiazoyl-2-yl)-2,5-diphenyltetrazolium bromide assay. Moreover, 3-week culture of hWJ-MSCs on scaffolds, immersed in osteogenic medium, rendered the microenvironment in favor of hWJ-MSCs differentiation into osteoblast cells and extracellular matrix secretion. Finally, osteoblasts were immunologically positive for various osteogenic markers including osteocalcin, osteopontin, osteonectin, and alkaline phosphatase. Present findings indicate that nHA/CS/Gel scaffold appropriately harbored hWJ-MSCs, stimulating their growth, migration, proliferation, and differentiation. hWJ-MSCs-loaded nHA/CS/gel substitute may therefore be considered as a suitable platform for the rising demand in in vivo bone repair studies. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 107A: 1166-1175, 2019.

Identifiants

pubmed: 30636089
doi: 10.1002/jbm.a.36608
doi:

Substances chimiques

Antigens, Differentiation 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1166-1175

Subventions

Organisme : Iran National Science Foundation (INSF)
ID : 92002917
Pays : International

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Zahra Jamalpoor (Z)

Trauma Research Center, Aja University of Medical Sciences, Tehran, Iran.

Nafise Taromi (N)

Department of Medical Biotechnology, Faculty of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran.
Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.

Mansooreh Soleimani (M)

Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Department of Anatomy, Iran University of Medical Sciences, Tehran, Iran.

Masoumeh Foroutan Koudehi (MF)

Biomaterial Laboratory, Faculty of Medicine, Aja University of Medical Sciences, Tehran, Iran.

Alireza Asgari (A)

Aerospace Medicine Research Center, Aja University of Medical Sciences, Tehran, Iran.

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