Charles A. O’Brien
Professor of Medicine
Also affiliated: National University of Ireland (1914); Charles University (1995); University of Arkansas Medical Center (1995–2026); Royal Navy (1914); University of Oklahoma Medical Center (1992); Oklahoma Medical Research Foundation (1989–1995); Yale University (1993–1994); Arkansas Cardiology (2023); Central Arkansas Veterans Healthcare System (2001–2026); Geriatric Research Education and Clinical Center (1997–1998); Winthrop Rockefeller Foundation (2024); Bone Health and Osteoporosis Foundation (2002–2016); University of Oklahoma Health Sciences Center (1989–1990); Centers for Medicare and Medicaid Services (1995); University of Pennsylvania (2024); University of Oklahoma (1990–1995); The University of Texas Health Science Center at Houston (1989); KU Leuven (2016)
Faculty Researcher
Internal Med, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Charles A. O’Brien, Professor of Medicine in the Department of Internal Medicine at the University of Arkansas for Medical Sciences, studies bone biology, focusing on cellular mechanisms of bone remodeling and disease. His research investigates the roles of osteoblasts and osteoclasts, key cell types involved in bone formation and resorption, respectively. O'Brien has received significant federal funding for his work, including over $2.9 million from the National Institutes of Health (NIH) for projects such as the Center for Musculoskeletal Disease Research and Osteocyte Control of Bone Remodeling.
His recent publications explore topics including the function of osteocytes in bone loss following medication discontinuation, the NAD salvage pathway's role in skeletal development, and the identification of senescent osteocytes contributing to bone destruction in breast cancer metastasis. O'Brien's laboratory also employs advanced techniques like CRISPR interference for cell type-specific gene editing. His scholarship metrics include an h-index of 64, with 187 publications and over 17,000 citations, highlighting his impact in the field. He actively collaborates with researchers at the University of Arkansas for Medical Sciences, including Elena Ambrogini, Olivia Reyes-Castro, Maria Almeida, and Hayley M. Sabol.
Metrics
- h-index: 64
- Publications: 188
- Citations: 17,838
Selected Publications
-
Protocol for the enrichment of endosteal and periosteal mesenchymal cells from murine bone for single-cell transcriptome analysis (2026)
-
A transcriptomic-driven segmentation and cell simulation framework for high-resolution spatial transcriptomics and cell-cell communication (2026)
-
Mechanistic insights into the pathogenesis and therapeutic recalcitrance of <i>Staphylococcus aureus</i> osteomyelitis (2026)
-
Deletion of the scavenger receptor Scarb1 in osteoblast progenitors and myeloid cells does not affect bone mass (2025)
-
The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone (2025)
-
Mechanisms of mitochondrial reactive oxygen species action in bone mesenchymal cells (2025)
-
Potent suppression of bone remodeling by denosumab does not blunt the anabolic response to romosozumab in mice (2025)
-
Mechanisms of mitochondrial reactive oxygen species action in bone mesenchymal cells (2025)
Federal Grants 5 $2,988,579 total
Different consequences of cellular aging in cortical versus cancellous bone- Resubmission
Grants & Funding
As listed on this researcher's institutional profile. Federal awards with verified records are shown above.
- Center for Musculoskeletal Disease Research (COBRE) NIH/Nat. Inst. of General Medical Sciences Principal Investigator
- In Vivo Regulation of IL6 and IL6R Gene Expression NIH/Nat. Inst. of Arthritis & Musculoskeletal & Skin Diseases Principal Investigator
- ABI C. OBrien NIH COBRE FY26 Y4 State of Arkansas Principal Investigator
- RANKL and Lymphocyte Mediated Bone Loss Veterans Administration Principal Investigator
- Center for Studies of Host Response to Cancer Therapy NIH Co-Investigator
- IN VIVO REGULATION OF IL6 AND IL6R GENE EXPRESSION NIH Principal Investigator
- Molecular and Cellular Mechanisms of Osteoporosis NIH Co-Investigator
- A Transgenic Rat for Noninvasive Assessment of Chondrogenic Activity in vivo NIH Co-Investigator
- Different consequences of cellular aging in cortical versus cancellous bone NIH/Nat. Inst. on Aging Co-Principal Investigator
Collaboration Network
Top Collaborators
- Reduced osteoprotegerin expression by osteocytes may contribute to rebound resorption after denosumab discontinuation
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- The NAD salvage pathway in mesenchymal cells is indispensable for skeletal development in mice
- Single-Cell Transcriptomic Analysis Identifies Senescent Osteocytes That Trigger Bone Destruction in Breast Cancer Metastasis
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
Showing 5 of 10 shared publications
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- The NAD salvage pathway in mesenchymal cells is indispensable for skeletal development in mice
- RETRACTED: Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass
- Mechanisms of mitochondrial reactive oxygen species action in bone mesenchymal cells
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
Showing 5 of 9 shared publications
- Reduced osteoprotegerin expression by osteocytes may contribute to rebound resorption after denosumab discontinuation
- Single-Cell Transcriptomic Analysis Identifies Senescent Osteocytes That Trigger Bone Destruction in Breast Cancer Metastasis
- Single-cell Transcriptome Analysis Identifies Senescent Osteocytes as Contributors to Bone Destruction in Breast Cancer Metastasis
- Deletion of the scavenger receptor Scarb1 in osteoblast progenitors does not affect bone mass
- RETRACTED: Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass
Showing 5 of 8 shared publications
- Reduced osteoprotegerin expression by osteocytes may contribute to rebound resorption after denosumab discontinuation
- Single-cell Transcriptome Analysis Identifies Senescent Osteocytes as Contributors to Bone Destruction in Breast Cancer Metastasis
- Deletion of the scavenger receptor Scarb1 in osteoblast progenitors does not affect bone mass
- RETRACTED: Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass
- Deletion of the Scavenger Receptor Scarb1 in Myeloid Cells Does Not Affect Bone Mass
Showing 5 of 7 shared publications
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- The NAD salvage pathway in mesenchymal cells is indispensable for skeletal development in mice
- Single-Cell Transcriptomic Analysis Identifies Senescent Osteocytes That Trigger Bone Destruction in Breast Cancer Metastasis
- Single-cell Transcriptome Analysis Identifies Senescent Osteocytes as Contributors to Bone Destruction in Breast Cancer Metastasis
- Mechanisms of mitochondrial reactive oxygen species action in bone mesenchymal cells
Showing 5 of 7 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
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
- 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
Showing 5 of 6 shared publications
- Reduced osteoprotegerin expression by osteocytes may contribute to rebound resorption after denosumab discontinuation
- Deletion of a putative promoter-proximal Tnfsf11 regulatory region in mice does not alter bone mass or Tnfsf11 expression in vivo
- CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system
- Potent suppression of bone remodeling by denosumab does not blunt the anabolic response to romosozumab in mice
- A new <i>Col1a1</i> conditional knock-in mouse model to study osteogenesis imperfecta
- Deletion of the scavenger receptor Scarb1 in osteoblast progenitors does not affect bone mass
- RETRACTED: Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass
- Deletion of the Scavenger Receptor Scarb1 in Myeloid Cells Does Not Affect Bone Mass
- Retraction notice to “Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass” [Bone 170(2023) 116702]
- OR27-02 The Bone Anabolic Effect Of An Antibody Blocking Oxidized Phospholipids Is Associated With An Increase In Wnt10b In Osteoblasts.
- Reduced osteoprotegerin expression by osteocytes may contribute to rebound resorption after denosumab discontinuation
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- Potent suppression of bone remodeling by denosumab does not blunt the anabolic response to romosozumab in mice
- Mechanisms of mitochondrial reactive oxygen species action in bone mesenchymal cells
- 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
- 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
- Deletion of the scavenger receptor Scarb1 in osteoblast progenitors does not affect bone mass
- RETRACTED: Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass
- Deletion of the Scavenger Receptor Scarb1 in Myeloid Cells Does Not Affect Bone Mass
- Retraction notice to “Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass” [Bone 170(2023) 116702]
- Deletion of the scavenger receptor Scarb1 in osteoblast progenitors does not affect bone mass
- RETRACTED: Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass
- Deletion of the Scavenger Receptor Scarb1 in Myeloid Cells Does Not Affect Bone Mass
- Retraction notice to “Deletion of the scavenger receptor Scarb1 in myeloid cells does not affect bone mass” [Bone 170(2023) 116702]
- The NAD salvage pathway in mesenchymal cells is indispensable for skeletal development in mice
- Single-Cell Transcriptomic Analysis Identifies Senescent Osteocytes That Trigger Bone Destruction in Breast Cancer Metastasis
- Single-cell Transcriptome Analysis Identifies Senescent Osteocytes as Contributors to Bone Destruction in Breast Cancer Metastasis
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- RANKL-mediated osteoclast formation is required for bone loss in a murine model of Staphylococcus aureus osteomyelitis
- Potent suppression of bone remodeling by denosumab does not blunt the anabolic response to romosozumab in mice
- A framework for defining mesenchymal cell types associated with murine periosteal and endosteal bone
- The NAD salvage pathway in mesenchymal cells is indispensable for skeletal development in mice
- Mechanisms of mitochondrial reactive oxygen species action in bone mesenchymal cells
- The Aging Landscape by <scp>scRNAseq</scp> of Mesenchymal Lineage Cells in Mouse Bone
Similar Researchers
Based on overlapping research topics