Jinhu Xiong
Associate Professor
faculty
Orthopaedics Surgery, College of Medicine
Research Areas
Links
Biography and Research Information
OverviewAI-generated summary
Jinhu Xiong, an Associate Professor in Orthopaedics Surgery at the University of Arkansas for Medical Sciences, investigates bone biology and the mechanisms of bone loss, particularly in the context of aging. His research focuses on cellular and molecular pathways that regulate bone homeostasis and strength.
Xiong's work includes studies on osteocytes and their role in mechanotransduction, the process by which cells sense and respond to mechanical forces. He has published research examining the function of the Piezo1 channel in bone, its influence on mitochondrial activity, and its potential role in mitigating age-associated bone loss. His laboratory also explores the identity and function of mesenchymal cell types involved in bone formation and remodeling, as well as the impact of autophagy regulators on bone mass and strength.
His research has been supported by federal grants, including a $324,368 award from the NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases to study the role of Piezo1 in bone homeostasis and mechanotransduction. Xiong is a highly cited researcher with an h-index of 22 based on 39 publications. He collaborates with researchers at the University of Arkansas for Medical Sciences, including Melda Onal, Charles A. O’Brien, Maria Almeida, and Ha‐Neui Kim.
Metrics
- h-index: 22
- Publications: 40
- Citations: 4,272
Selected Publications
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Dissecting primary versus secondary effects of osteogenesis imperfecta on abnormal lung development and function (2026)
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The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone (2025)
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Different effects of moderate tibial loading and Yoda1 on breast cancer-induced osteolysis in aged mice (2025)
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Mitochondrial oxidative stress or decreased autophagy in osteoblast lineage cells is not sufficient to mimic the deleterious effects of aging on bone mechanoresponsiveness (2025)
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Piezo1 expression in mature osteocytes is dispensable for the skeletal response to mechanical loading (2024)
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Mitigating aging and doxorubicin induced bone loss in mature mice via mechanobiology based treatments (2024)
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Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone (2024)
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A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone (2023)
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Piezo1 opposes age‐associated cortical bone loss (2023)
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Piezo1 stimulates mitochondrial function via <scp>cAMP</scp> signaling (2022)
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Deletion of a putative promoter-proximal Tnfsf11 regulatory region in mice does not alter bone mass or Tnfsf11 expression in vivo (2021)
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New Advances in Osteocyte Mechanotransduction (2021)
Federal Grants 1 $324,368 total
The role of Piezo1 in bone homeostasis and mechanotransduction
Grants & Funding
- Osteocyte Control of Bone Remodeling NIH/Nat. Inst. of Arthritis & Musculoskeletal & Skin Diseases Co-Investigator
- Center for Musculoskeletal Disease Research (CMDR) NIH/Nat. Inst. of General Medical Sciences Co-Investigator
- The role of Piezo 1 in bone homeostasis and mechanotransduction NIH/Nat. Inst. of Arthritis & Musculoskeletal & Skin Diseases Principal Investigator
Collaboration Network
Top Collaborators
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- Deletion of a putative promoter-proximal Tnfsf11 regulatory region in mice does not alter bone mass or Tnfsf11 expression in vivo
- Elevation of master autophagy regulator Tfeb in osteoblast lineage cells increases bone mass and strength
- Mitochondrial oxidative stress or decreased autophagy in osteoblast lineage cells is not sufficient to mimic the deleterious effects of aging on bone mechanoresponsiveness
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
Showing 5 of 6 shared publications
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- Deletion of a putative promoter-proximal Tnfsf11 regulatory region in mice does not alter bone mass or Tnfsf11 expression in vivo
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
- A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone
- Local Production of Osteoprotegerin by Osteoblasts Suppresses Bone Resorption
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- Piezo1 stimulates mitochondrial function via <scp>cAMP</scp> signaling
- Elevation of master autophagy regulator Tfeb in osteoblast lineage cells increases bone mass and strength
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
- A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- Elevation of master autophagy regulator Tfeb in osteoblast lineage cells increases bone mass and strength
- Mitochondrial oxidative stress or decreased autophagy in osteoblast lineage cells is not sufficient to mimic the deleterious effects of aging on bone mechanoresponsiveness
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
- A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone
- New Advances in Osteocyte Mechanotransduction
- Piezo1 stimulates mitochondrial function via <scp>cAMP</scp> signaling
- Mitigating aging and doxorubicin induced bone loss in mature mice via mechanobiology based treatments
- Different effects of moderate tibial loading and Yoda1 on breast cancer-induced osteolysis in aged mice
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- Piezo1 stimulates mitochondrial function via <scp>cAMP</scp> signaling
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
- A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone
- Mitochondrial oxidative stress or decreased autophagy in osteoblast lineage cells is not sufficient to mimic the deleterious effects of aging on bone mechanoresponsiveness
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
- Blocking Oxidized Phospholipids Attenuates the Age-Associated, but Not the Ovariectomy- or Unloading- Induced, Bone Loss in Mice
- Deletion of a putative promoter-proximal Tnfsf11 regulatory region in mice does not alter bone mass or Tnfsf11 expression in vivo
- Local Production of Osteoprotegerin by Osteoblasts Suppresses Bone Resorption
- Dissecting primary versus secondary effects of osteogenesis imperfecta on abnormal lung development and function
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- Elevation of master autophagy regulator Tfeb in osteoblast lineage cells increases bone mass and strength
- A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- Mitochondrial oxidative stress or decreased autophagy in osteoblast lineage cells is not sufficient to mimic the deleterious effects of aging on bone mechanoresponsiveness
- A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone
- Elevation of master autophagy regulator Tfeb in osteoblast lineage cells increases bone mass and strength
- Mitochondrial oxidative stress or decreased autophagy in osteoblast lineage cells is not sufficient to mimic the deleterious effects of aging on bone mechanoresponsiveness
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
- New Advances in Osteocyte Mechanotransduction
- Piezo1 stimulates mitochondrial function via <scp>cAMP</scp> signaling
- Local Production of Osteoprotegerin by Osteoblasts Suppresses Bone Resorption
- Blocking Oxidized Phospholipids Attenuates the Age-Associated, but Not the Ovariectomy- or Unloading- Induced, Bone Loss in Mice
- Piezo1 opposes age‐associated cortical bone loss
- Blocking Oxidized Phospholipids Attenuates the Age-Associated, but Not the Ovariectomy- or Unloading- Induced, Bone Loss in Mice
- Deletion of a putative promoter-proximal Tnfsf11 regulatory region in mice does not alter bone mass or Tnfsf11 expression in vivo
- Local Production of Osteoprotegerin by Osteoblasts Suppresses Bone Resorption
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