Jinhu Xiong

Federal Grant PI High Impact

Associate Professor

University of Arkansas for Medical Sciences

faculty

Orthopaedics Surgery, College of Medicine

jxiong@uams.edu

22 h-index 38 pubs 4,164 cited

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Biography and Research Information

OverviewAI-generated summary

Jinhu Xiong is an Associate Professor in Orthopaedics Surgery at the University of Arkansas for Medical Sciences. His research focuses on bone mechanobiology and the role of specific cellular signaling pathways in maintaining skeletal health, particularly in the context of aging and disease. Xiong has received federal funding from the NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases for his work investigating the function of Piezo1 in bone homeostasis and mechanotransduction. His laboratory actively studies how mechanical forces influence bone cells and seeks to develop mechanobiology-based treatments to mitigate bone loss associated with aging and chemotherapy.

Xiong's recent publications explore various aspects of bone biology, including the function of the Piezo1 channel in osteocytes and its impact on mitochondrial signaling, the identity of mesenchymal cell types in bone, and strategies to counteract age-related bone loss. He has also investigated the role of autophagy regulators in bone mass and strength. His scholarly work has resulted in a h-index of 22 and over 4,000 citations across his 38 publications. He collaborates with researchers at the University of Arkansas for Medical Sciences, including Melda Onal, Charles A. O’Brien, and Maria Almeida.

Metrics

  • h-index: 22
  • Publications: 38
  • Citations: 4,164

Selected Publications

  • The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone (2025) DOI
  • Different effects of moderate tibial loading and Yoda1 on breast cancer-induced osteolysis in aged mice (2025) DOI
  • Mitochondrial oxidative stress or decreased autophagy in osteoblast lineage cells is not sufficient to mimic the deleterious effects of aging on bone mechanoresponsiveness (2025) DOI
  • Piezo1 expression in mature osteocytes is dispensable for the skeletal response to mechanical loading (2024) DOI
  • Mitigating aging and doxorubicin induced bone loss in mature mice via mechanobiology based treatments (2024) DOI
  • Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone (2024) DOI
  • A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone (2023) DOI
  • Piezo1 opposes age‐associated cortical bone loss (2023) DOI
  • Piezo1 stimulates mitochondrial function via <scp>cAMP</scp> signaling (2022) DOI
  • Deletion of a putative promoter-proximal Tnfsf11 regulatory region in mice does not alter bone mass or Tnfsf11 expression in vivo (2021) DOI
  • New Advances in Osteocyte Mechanotransduction (2021) DOI

Federal Grants 1 $324,368 total

NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases Contact PI Aug 2020 - Jun 2026

The role of Piezo1 in bone homeostasis and mechanotransduction

National Institute of Arthritis and Musculoskeletal and Skin Diseases $324,368 R01

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

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