Publications by authors named "Guanghao Chi"

Article Synopsis
  • Astrocytes function as immune cells that release chemokines, specifically CCL5, which attract leukocytes to sites of spinal cord injury (SCI), leading to increased inflammation.
  • The study found that levels of CCL5 increase in parallel with HMGB1 after SCI, and blocking HMGB1 significantly lowers CCL5 levels.
  • HMGB1 activates the production of CCL5 in astrocytes through specific receptors and pathways, and inhibiting HMGB1 can reduce inflammation and improve recovery after SCI, suggesting new potential treatments for CNS inflammation.
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Objectives: The OPG/RANKL signal pathway was important regulation mechanism of bone remodeling cycle, but the effect of osteoprotegerin (OPG) and RANKL in osteoporosis was uncertain. We did a systematic review with meta-analysis to assess the association between serum OPG/RANKL and osteoporosis.

Methods: The systematic search, data extraction, critical appraisal, and meta-analysis were performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement.

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Large bone defects face a high risk of infection, which can also lead to bone homeostasis disorders. This seriously hinders the bone healing process; therefore, the help of a dual-functional scaffold that has both anti-infection and bone-homeostasis-regulating capacities is needed in the treatment of infected bone defects. In this study, a 3D printed dual-functional scaffold composed of poly-ε-caprolactone (PCL), mesoporous bioactive glasses (MBG), and gallium (Ga) was produced.

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Study Design: Retrospective single-center study.

Objective: We want to know whether interleukin (IL)-10-secreting regulatory T cells (Treg) promote the new bone formation (NBF) through suppressing TH17 in ankylosing spondylitis (AS).

Summary Of Background Data: NBF in AS is unknown.

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Genetically modified mesenchymal stem cells have been used in attempts to increase the expression of interleukin‑1 receptor antagonist (IL‑1Ra); however, the attempts thus far have been unsuccessful. The aim of the present study was to investigate whether the lentivirus transduced IL‑1Ra gene was able to be stably expressed in murine bone marrow‑derived mesenchymal stem cells (mBMSCs) in vitro. In the present study, third generation lentiviral (Lv) vectors transducing the IL‑1Ra/green fluorescent protein (copGFP) gene were constructed and transfected into mBMSCs to establish the Lv.

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