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Journal ArticleDOI

The effect of hyaluronan on osteoblast proliferation and differentiation in rat calvarial‐derived cell cultures

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TLDR
The findings suggest that HA has a molecular weight-specific and dose-specific mode of action that may enhance the osteogenic and osteoinductive properties of bone graft materials and substitutes due to its stimulatory effects on osteoblasts.
Abstract
Hyaluronan (or hyaluronic acid, HA) is an essential component of extracellular matrices. It interacts with other macromolecules and plays a predominant role in tissue morphogenesis, cell migration, differentiation, and adhesion. The cell signaling functions of HA are mediated through the CD-44 receptor and are dependent upon the molecular weight of the polymer. We hypothesized that an HA of appropriate molecular weight alone in optimal concentration may induce osteoblast differentiation and bone formation. Enzyme-digested calvarial-derived mesenchymal cells from 2-day-old newborn rats were cultured with the addition of HA of three different molecular weights (2300, 900, and 60 kDa). We added, 0.5, 1.0, and 2.0 mg/mL HA for each molecular weight to the medium at the first plating of cells. After 7 to 20 days in culture, cell proliferation and differentiation were evaluated by measuring thymidine incorporation, alkaline phosphatase activity, and osteocalcin gene expression. The effects of HA on bone formation were examined by using Alizarin red staining for mineralization. The results showed that low molecular weight HA (60 kDa) significantly stimulated cell growth, increased osteocalcin mRNA expression in a dose-dependent manner, but showed no apparent effects on alkaline phosphatase activity and bone mineralization. On the other hand, high-weight HA (900 and 2,300 kDa) significantly increased all the parameters examined, particularly alkaline phosphatase activity, in a dose-dependent manner and stimulated cell mineralization to 126% and 119% of the controls, respectively, in the 1.0 mg/mL dose. Our findings suggest that HA has a molecular weight-specific and dose-specific mode of action that may enhance the osteogenic and osteoinductive properties of bone graft materials and substitutes due to its stimulatory effects on osteoblasts.

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Natural origin biodegradable systems in tissue engineering and regenerative medicine: present status and some moving trends

TL;DR: In this review, the most studied and promising and recently proposed naturally derived polymers that have been suggested for tissue engineering applications are described and their blends with synthetic polymers are analysed, with special focus on polysaccharides and proteins.
Journal ArticleDOI

Hyaluronan blocks oligodendrocyte progenitor maturation and remyelination through TLR2

TL;DR: It is reported here that Toll-like receptor 2 (TLR2) is expressed by oligodendrocytes and is up-regulated in MS lesions and it is defined a mechanism controlling remyelination failure in MS where hyaluronan is degraded byhyaluronidases into hyalurin oligomers that block OPC maturation and remyElination through TLR2-MyD88 signaling.
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Hyaluronic acid hydrogels with controlled degradation properties for oriented bone regeneration.

TL;DR: The fastest and slowest degrading scaffolds seemed to result in more organized bone than the intermediate degrading scaffold, which was designed to degrade in 6-8 weeks to match the healing time, and healing could be enhanced by co-delivery of vascular endothelial growth factor along with BMP-2.
Journal ArticleDOI

Strategies for Directing the Differentiation of Stem Cells Into the Osteogenic Lineage In Vitro

TL;DR: This review critically examines the various strategies that could be used to direct the differentiation of stem cells into the osteogenic lineage in vitro and suggests that well‐defined and efficient protocols developed could provide useful in vitro models for studying osteogenesis and bone development.
Journal ArticleDOI

A comparative study on collagen type I and hyaluronic acid dependent cell behavior for osteochondral tissue bioprinting.

TL;DR: The behavior of chondrocytes and osteoblasts to hyaluronic acid (HA) and type I collagen (Col-1) hydrogels is examined and bioprinting-based approaches can be successfully applied for osteochondral tissue regeneration.
References
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Journal ArticleDOI

Angiogenesis induced by degradation products of hyaluronic acid.

TL;DR: Partial degradation products of sodium hyaluronate produced by the action of testicular hyaluridase induced an angiogenic response (formation of new blood vessels) on the chick chorioallantoic membrane.
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Hyaluronan-binding proteins in development, tissue homeostasis, and disease.

TL;DR: The high molecular weight glycosaminoglycan hyaluronan plays an important role in tissue remodeling during development, normal tissue homeostasis, and disease.
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Hyaluronan in morphogenesis.

TL;DR: In-vitro studies suggest strongly that interactions of hyaluronan with RHAMM or CD44 are involved in cell movement and proliferation, which are critical events in morphogenesis.
Journal Article

Bisphosphonates directly regulate cell proliferation, differentiation, and gene expression in human osteoblasts.

TL;DR: Osteoblast cell proliferation was decreased, and cytodifferentiation was increased in a dose-dependent manner in cultures treated with the bisphosphonate pamidronate, and the rate of bone formation was also increased in osteoblasts cultured with pamodronate.
Journal ArticleDOI

Hyaluronate in vasculogenesis

TL;DR: Limb buds of chicken embryos contain within the peripheral mesoderm an avascular zone that is rich in hyaluronic acid, which may play a role in determining the location of blood vessels in the embryo.
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