Hyaluronan hydrogels delivering BMP-6 for local targeting of malignant plasma cells and osteogenic differentiation of mesenchymal stromal cells.


Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
15 09 2019
Historique:
received: 19 03 2019
revised: 08 07 2019
accepted: 10 07 2019
pubmed: 16 7 2019
medline: 29 7 2020
entrez: 15 7 2019
Statut: ppublish

Résumé

Multiple myeloma is a malignant disease characterized by accumulation of clonal plasma cells in the bone marrow. Uncoupling of bone formation and resorption by myeloma cells leads to osteolytic lesions. These are prone to fracture and represent a possible survival space for myeloma cells under treatment causing disease relapse. Here we report on a novel approach suitable for local treatment of multiple myeloma based on hyaluronic acid (HA) hydrogels mimicking the physical properties of the bone marrow. The HA hydrogels are complexed with heparin to achieve sustained presentation and controlled release of bone morphogenetic protein 6 (BMP-6). Others and we have shown that BMP-6 induces myeloma cell apoptosis and bone formation. Using quartz crystal microbalance and enzyme-linked immunosorbent assay, we measured an initial surface density of 400 ng BMP6/cm

Identifiants

pubmed: 31302300
pii: S1742-7061(19)30498-2
doi: 10.1016/j.actbio.2019.07.018
pii:
doi:

Substances chimiques

BMP6 protein, human 0
Bone Morphogenetic Protein 6 0
Hydrogels 0
Hyaluronic Acid 9004-61-9

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

258-270

Informations de copyright

Copyright © 2019 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Auteurs

Anna Luise Grab (AL)

Labor für Myelomforschung, Medizinische Klinik V, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany; Institute of Physical Chemistry, Department of Biophysical Chemistry, Heidelberg University, Im Neuenheimer Feld 253, 69120 Heidelberg, Germany; Max Planck Institute for Medical Research, Department of Cellular Biophysics and Central Scientific Facility "Cellular Biotechnology", Jahnstr. 29, 69120 Heidelberg, Germany.

Anja Seckinger (A)

Labor für Myelomforschung, Medizinische Klinik V, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.

Patrick Horn (P)

Medizinische Klinik V, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 350, 69120 Heidelberg, Germany.

Dirk Hose (D)

Labor für Myelomforschung, Medizinische Klinik V, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany. Electronic address: Dirk.Hose@med.uni-heidelberg.de.

Elisabetta Ada Cavalcanti-Adam (EA)

Institute of Physical Chemistry, Department of Biophysical Chemistry, Heidelberg University, Im Neuenheimer Feld 253, 69120 Heidelberg, Germany; Max Planck Institute for Medical Research, Department of Cellular Biophysics and Central Scientific Facility "Cellular Biotechnology", Jahnstr. 29, 69120 Heidelberg, Germany. Electronic address: eacavalcanti@mr.mpg.de.

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Classifications MeSH