Background: Collagen is a well-established and important biomaterial that could be used to help meet significant medical needs for various soft-tissue replacements. Many efforts to create engineered soft-tissue constructs by seeding cells within collagen gels have been hampered because constituent cells contract collagen gels over time, resulting in a construct that is only a fraction of the original size and that contains a cell population that has suffered a large degree of cell death. However, the presence of embedded short collagen fibers has been shown to significantly limit contraction and dramatically enhance permeability in fibroblast-seeded collagen gels.
Methods: Five volume fractions of short collagen fibers were embedded in fibroblast-seeded collagen gels. Collagen gel contraction (n > or = 4 for all groups) and cell viability (n > or = 3 for all groups) were examined after up to 2 weeks in culture.
Results: The present study demonstrated that increasing the volume fraction of short collagen fibers in fibroblast-seeded collagen gels correspondingly reduced the amount of gel contraction without negatively impacting cell viability after 2 weeks of culture. Furthermore, operating curves that describe the quantitative relationships between the contraction of fibroblast-seeded collagen gel/collagen fiber composite biomaterials, time in culture, and volume fraction of embedded fibers were obtained.
Conclusion: The resulting operating curves enable investigators to tailor initial fabrication procedures to ultimately yield cell-seeded collagen composites of specifically desired sizes-a critical step toward developing clinically useful engineered soft-tissue constructs.
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http://dx.doi.org/10.1097/01.prs.0000246316.87802.b4 | DOI Listing |
Avicenna J Med Biotechnol
January 2023
Nanobiotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Background: In this study we differentially showed the effects of cell-seeded bilayer scaffold wound dressing in accelerating healing process in diabetic ulcers that still remains as a major clinical challenge. The aim of the study was to compare immunomodulatory and angiogenic activity, and regenerative effect differences between Menstrual blood-derived Stem Cells (MenSCs) and foreskin-derived keratinocytes/fibroblasts.
Methods: The streptozotocin-induced diabetic mice model was developed in male C57/BL6 mice.
Int J Mol Sci
February 2023
Department of Mining and Materials Engineering, McGill University, Montreal, QC H3A 0C5, Canada.
Reconstituted hydrogels based on the self-assembly of acid-solubilized collagen molecules have been extensively used as in vitro models and precursors in biofabrication processes. This study investigated the effect of fibrillization pH-ranging from 4 to 11-on real-time rheological property changes during the gelation of collagen hydrogels and its interplay with the properties of subsequently biofabricated dense collagen matrices generated via automated gel aspiration-ejection (GAE). A contactless, nondestructive technique was used to characterize the temporal progression in shear storage modulus (G', or stiffness) during collagen gelation.
View Article and Find Full Text PDFJ Biomed Mater Res B Appl Biomater
March 2023
Marquette University School of Dentistry, Milwaukee, Wisconsin, USA.
The development of vascularized scaffolds remains one of the major challenges in tissue engineering, and co-culturing with endothelial cells is known as one of the possible approaches for this purpose. In this approach, optimization of cell culture conditions, scaffolds, and fabrication techniques is needed to develop tissue equivalents that will enable in vitro formation of a capillary network. Prevascularized equivalents will be more physiologically comparable to the native tissues and potentially prevent insufficient vascularization after implantation.
View Article and Find Full Text PDFTissue Eng Part C Methods
November 2022
School of Dentistry, Institute of Clinical Sciences, University of Birmingham, Birmingham, United Kingdom.
Air-liquid interface (ALI) cultures are used to produce stratified epithelial tissues , notably for the production of oral mucosal equivalents. Currently, there are few purpose-built devices, which aim to enhance the ease and reproducibility of generating such tissue. Most ALI cultures utilize stainless steel grids or cell culture inserts to elevate the matrix or scaffold to the surface of the culture media.
View Article and Find Full Text PDFFront Bioeng Biotechnol
July 2022
Roy J. Carver Department of Biomedical Engineering, College of Engineering, University of Iowa, Iowa City, IA, United States.
Tissue fibrosis is a major health issue that impacts millions of people and is costly to treat. However, few effective anti-fibrotic treatments are available. Due to their central role in fibrotic tissue deposition, fibroblasts and myofibroblasts are the target of many therapeutic strategies centered primarily on either inducing apoptosis or blocking mechanical or biochemical stimulation that leads to excessive collagen production.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!