ArticleIn vitro cellular & developmental biology. Animal1997
Skeletal muscle satellite cells cultured in simulated microgravity.
Article in In vitro cellular & developmental biology. Animal, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed, 66 citations in OpenAlex.
- PIEZO1 Mediates Myoblast Proliferation Under Simulated Microgravity.Annals of the New York Academy of Sciences · 2026Article
- Microcarrier-seeded muscle cells exhibit delayed differentiation in simulated microgravity compared to a terrestrial bioreactor.NPJ science of food · 2025Article
- Attachment promoting compounds significantly enhance cell proliferation and purity of bovine satellite cells grown on microcarriers in the absence of serum.Frontiers in bioengineering and biotechnology · 2024Article
- Muscle Atrophy Marker Expression Differs between Rotary Cell Culture System and Animal Studies.BioMed research international · 2019Article
- Microfluidics-based 3D cell culture models: Utility in novel drug discovery and delivery research.Bioengineering & translational medicine · 2016Review
- Use of flow, electrical, and mechanical stimulation to promote engineering of striated muscles.Annals of biomedical engineering · 2014Review
- RCCS enhances EOE cell proliferation and their differentiation into ameloblasts.Molecular biology reports · 2012Article
- Effects of simulated microgravity on expression profile of microRNA in human lymphoblastoid cells.The Journal of biological chemistry · 2011Article
- A hitchhiker's guide to mechanobiology.Developmental cell · 2011Review
- [Bioreactors in tissue culture].HNO · 2008Review
- Transplantation of engineered bone tissue using a rotary three-dimensional culture system.In vitro cellular & developmental biology. Animal · 2007Article
- Bioreactor-based bone tissue engineering: the influence of dynamic flow on osteoblast phenotypic expression and matrix mineralization.Proceedings of the National Academy of Sciences of the United States of America · 2004Article
- Differentiation of mammalian skeletal muscle cells cultured on microcarrier beads in a rotating cell culture system.Medical & biological engineering & computing · 2000Article
- Characterization of aggregation and protein expression of bovine corneal endothelial cells as microcarrier cultures in a rotating-wall vessel.Cytotechnology · 2000Article
- Neonatal rat heart cells cultured in simulated microgravity.In vitro cellular & developmental biology. Animal · 1997Article
- Three-dimensional adipose tissue model using low shear bioreactors.In vitro cellular & developmental biology. AnimalArticle
- A novel in vitro three-dimensional skeletal muscle model.In vitro cellular & developmental biology. AnimalArticle
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Satellite cells are postnatal myoblasts responsible for providing additional nuclei to growing or regenerating muscle cells. Satellite cells retain the capacity to proliferate and differentiate in vitro and, therefore, provide a useful model to study postnatal muscle development. Most culture systems used to study postnatal muscle development are limited by the two-dimensional (2-D) confines of the culture dish. Limiting proliferation and differentiation of satellite cells in 2-D could potentially limit cell-cell contacts important for developing the level of organization in skeletal muscle obtained in vivo. Culturing satellite cells on microcarrier beads suspended in the High-Aspect-Ratio-Vessel (HARV) designed by NASA provides a low shear, three-dimensional (3-D) environment to study muscle development. Primary cultures established from anterior tibialis muscles of growing rats (approximately 200 gm) were used for all studies and were composed of greater than 75% satellite cells. Different inoculation densities did not affect the proliferative potential of satellite cells in the HARV. Plating efficiency, proliferation, and glucose utilization were compared between 2-D culture and 3-D HARV culture. Plating efficiency (cells attached divided by cells plated x 100) was similar between the two culture systems. Proliferation was reduced in HARV cultures and this reduction was apparent for both satellite cells and nonsatellite cells. Furthermore, reduction in proliferation within the HARV could not be attributed to reduced substrate availability because glucose levels in medium from HARV and 2-D cell culture were similar. Morphologically, microcarrier beads within the HARV were joined together by cells into 3-D aggregates composed of greater than 10 beads/aggregate. Aggregation of beads did not occur in the absence of cells. Myotubes were often seen on individual beads or spanning the surface of two beads. In summary, proliferation and differentiation of satellite cells on microcarrier beads within the HARV bioreactor results in a 3-D level of organization that could provide a more suitable model to study postnatal muscle development than is currently available with standard culture methods.
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