Please use this identifier to cite or link to this item: https://doi.org/10.21256/zhaw-4755
Title: Macromolecular crowding directs extracellular matrix organization and mesenchymal stem cell behavior
Authors : Zeiger, Adam S.
Loe, Felicia C.
Li, Ran
Raghunath, Michael
Van Vliet, Krystyn J.
Published in : PLOS ONE
Volume(Issue) : 7
Issue : 5
Pages : e37904
Publisher / Ed. Institution : Public Library of Science
Issue Date: 2012
License (according to publishing contract) : CC BY 4.0: Attribution 4.0 International
Type of review: Peer review (Publication)
Language : English
Subjects : Western blotting; Cell adhesion; Cell culture techniques; Cell cycle; Cell differentiation; Cell movement; Extracellular matrix; Ficoll; Immunohistochemistry; Macromolecular substances; Mesenchymal stromal cells; Microbial interactions; Atomic force microscopy; Tissue engineering
Subject (DDC) : 570: Biology
Abstract: Microenvironments of biological cells are dominated in vivo by macromolecular crowding and resultant excluded volume effects. This feature is absent in dilute in vitro cell culture. Here, we induced macromolecular crowding in vitro by using synthetic macromolecular globules of nm-scale radius at physiological levels of fractional volume occupancy. We quantified the impact of induced crowding on the extracellular and intracellular protein organization of human mesenchymal stem cells (MSCs) via immunocytochemistry, atomic force microscopy (AFM), and AFM-enabled nanoindentation. Macromolecular crowding in extracellular culture media directly induced supramolecular assembly and alignment of extracellular matrix proteins deposited by cells, which in turn increased alignment of the intracellular actin cytoskeleton. The resulting cell-matrix reciprocity further affected adhesion, proliferation, and migration behavior of MSCs. Macromolecular crowding can thus aid the design of more physiologically relevant in vitro studies and devices for MSCs and other cells, by increasing the fidelity between materials synthesized by cells in vivo and in vitro.
Departement: Life Sciences and Facility Management
Organisational Unit: Institute of Chemistry and Biotechnology (ICBT)
Publication type: Article in scientific Journal
DOI : 10.1371/journal.pone.0037904
10.21256/zhaw-4755
ISSN: 1932-6203
URI: https://digitalcollection.zhaw.ch/handle/11475/12212
Appears in Collections:Publikationen Life Sciences und Facility Management

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