Publications by authors named "Yasunori Inada"

The polarization balance of M1/M2 macrophages with different functions is important in osteogenesis and bone repair processes. In a previous study, we succeeded in developing honeycomb tricalcium phosphate (TCP), which is a cylindrical scaffold with a honeycomb arrangement of straight pores, and we demonstrated that TCP with 300 and 500 μm pore diameters (300TCP and 500TCP) induced bone formation within the pores. However, the details of the influence of macrophage polarization on bone formation using engineered biomaterials, especially with respect to the geometric structure of the artificial biomaterials, are unknown.

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Article Synopsis
  • Bone marrow regeneration is challenging due to its complex structure, but a study developed a honeycomb-shaped tricalcium phosphate (TCP) scaffold to promote bone marrow formation.
  • The study tested two versions of the TCP, 300μm and 500μm pore diameters (300TCP and 500TCP) in rats, finding that 300TCP promoted a larger area of bone marrow structure with more blood vessels and hematopoietic cells.
  • Results indicated that 300TCP effectively supported a niche for hematopoietic stem cells, suggesting it may be the optimal scaffold design for promoting bone marrow regeneration.
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Tumor angiogenesis is one of the hallmarks of solid tumor development. The progressive tumor cells produce the angiogenic factors and promote tumor angiogenesis. However, how the tumor stromal cells influence tumor vascularization is still unclear.

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  • The study investigates how stromal cells from gum (G-SCs) and periodontal ligament (P-SCs), as well as dermal fibroblasts (HDFs), influence bone resorption and osteoclast activity in the context of oral squamous cell carcinoma (OSCC).
  • G-SCs were found to enhance bone invasion and activate osteoclasts, while P-SCs inhibited bone resorption and promoted osteoclast proliferation but had a limited effect on activation.
  • The research also highlighted that G-SCs significantly affected several protein expressions related to bone invasion, while P-SCs had a more subdued impact, suggesting distinct regulatory mechanisms in bone invasion driven by these different stromal cells
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Stromal cells in the tumor microenvironment (TME) can regulate the progression of numerous types of cancer; however, the bone invasion of oral squamous cell carcinoma (OSCC) has been poorly investigated. In the present study, the effect of verrucous SCC‑associated stromal cells (VSCC‑SCs), SCC‑associated stromal cells (SCC‑SCs) and human dermal fibroblasts on bone resorption and the activation of HSC‑3 osteoclasts were examined by hematoxylin and eosin, AE1/3 (pan‑cytokeratin) and tartrate‑resistant acid phosphatase staining. In addition, the expression levels of matrix metalloproteinase (MMP)9, membrane‑type 1 MMP (MT1‑MMP), Snail, receptor activator of NF‑κB ligand (RANKL) and parathyroid hormone‑related peptide (PTHrP) in the bone invasion regions of HSC‑3 cells were examined by immunohistochemistry.

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In recent years, there has been increasing interest in the treatment of bone defects using undifferentiated mesenchymal stem cells (MSCs) in vivo. Recently, dental pulp has been proposed as a promising source of pluripotent mesenchymal stem cells (MSCs), which can be used in various clinical applications. Dentin is the hard tissue that makes up teeth, and has the same composition and strength as bone.

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Recently, dental pulp has been attracting attention as a promising source of multipotent mesenchymal stem cells (MSCs) for various clinical applications of regeneration fields. To date, we have succeeded in establishing rat dental pulp-derived cells showing the characteristics of odontoblasts under in vitro conditions. We named them Tooth matrix-forming, GFP rat-derived Cells (TGC).

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