Neha S. Dole
Assistant Professor
faculty
Physiology and Cell Biology, College of Medicine
Research Areas
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Biography and Research Information
OverviewAI-generated summary
Neha S. Dole, Assistant Professor in the Department of Physiology and Cell Biology at the University of Arkansas for Medical Sciences, investigates the role of osteocytes in bone health and systemic metabolic regulation. Her research focuses on how these bone cells respond to mechanical stimuli and dietary factors, influencing bone quality and overall body function. Dole's work has explored the intricate signaling pathways within osteocytes, including the involvement of transforming growth factor beta (TGFβ) and microRNAs (miRNAs) such as miR-100 and miR-181a/b-1.
Her federally funded project, supported by a $140,899 grant from the NIH/National Institute of Diabetes and Digestive and Kidney Diseases, aims to unravel the role of osteocytes in metabolic dysfunction associated with obesity. This research investigates how factors like high-fat and high-carbohydrate diets impact bone fragility through TGF-β dependent mechanisms. Dole's publications also examine the effects of aging on osteocytic regulation of collagen integrity and bone quality, as well as the potential therapeutic benefits of agents like zoledronic acid in improving bone and muscle function.
Dole collaborates with researchers at the University of Arkansas for Medical Sciences, including Vivek Khanal, Madeline Carroll, Amy Y. Sato, and Ryan M. Allen, with whom she has co-authored multiple publications. Her scholarship metrics include an h-index of 13 and 27 total publications.
Metrics
- h-index: 14
- Publications: 27
- Citations: 598
Selected Publications
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Osteocytic Lipocalin-2 regulates bone formation locally through iron-dependent ferroptosis and Wnt suppression (2026)
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Global Transcriptional Profiling of Adipose Tissue Uncovers Unique Sex-Dependent Mechanisms in Acute Obesity: Implications for Adipose-Heart Interorgan Crosstalk (2025)
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Lipocalin-2 Regulates Osteocyte Ferroptosis and Osteocyte-Osteoblast Crosstalk via Wnt Signaling to Control Bone Formation (2025)
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High-fat and high-carbohydrate diets increase bone fragility through TGF-β–dependent control of osteocyte function (2024)
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miR181a/b-1 controls osteocyte metabolism and mechanical properties independently of bone morphology (2023)
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The Multifaceted Effects of Osteocytic TGFβ Signaling on the Skeletal and Extraskeletal Functions of Bone (2023)
Federal Grants 1 $140,899 total
Unraveling the role of osteocytes in metabolic dysfunction associated with obesity
Grants & Funding
- Role of subchondral bone osteocytes in post-traumatic osteoarthritis US Department of Defense Principal Investigator
- Unraveling the role of osteocytes in metabolic dysfunction associated with obesity NIH/Nat. Inst. of Diabetes & Digestive & Kidney Diseases Principal Investigator
- Unraveling the role of osteocytes in metabolic dysfunction associated with obesity NIH/Nat. Inst. of Diabetes & Digestive & Kidney Diseases Principal Investigator
- Vivek Khanal ASBMR 2025 President's Award American Society for Bone and Mineral Research Principal Investigator
- Role of subchondral bone osteocytes in post-traumatic osteoarthritis US Department of Defense Principal Investigator
- ABI P. Prather NIH T32 FY26 Y3 State of Arkansas Principal Investigator
Collaboration Network
Top Collaborators
- Fluid shear stress generates a unique signaling response by activating multiple TGFβ family type I receptors in osteocytes
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Mechanosensitive miR‐100 coordinates TGFβ and Wnt signaling in osteocytes during fluid shear stress
- High-fat and high-carbohydrate diets increase bone fragility through TGF-β–dependent control of osteocyte function
- The Multifaceted Effects of Osteocytic TGFβ Signaling on the Skeletal and Extraskeletal Functions of Bone
Showing 5 of 9 shared publications
- Fluid shear stress generates a unique signaling response by activating multiple TGFβ family type I receptors in osteocytes
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Mechanosensitive miR‐100 coordinates TGFβ and Wnt signaling in osteocytes during fluid shear stress
- High-fat and high-carbohydrate diets increase bone fragility through TGF-β–dependent control of osteocyte function
- miR181a/b-1 controls osteocyte metabolism and mechanical properties independently of bone morphology
Showing 5 of 6 shared publications
- Fluid shear stress generates a unique signaling response by activating multiple TGFβ family type I receptors in osteocytes
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- High-fat and high-carbohydrate diets increase bone fragility through TGF-β–dependent control of osteocyte function
- Age-related decline in osteocytic TGFβ signaling disrupts collagen integrity and bone quality
- Mechanosensitive miR‐100 coordinates TGFβ and Wnt signaling in osteocytes during fluid shear stress
- High-fat and high-carbohydrate diets increase bone fragility through TGF-β–dependent control of osteocyte function
- miR181a/b-1 controls osteocyte metabolism and mechanical properties independently of bone morphology
- High-fat and high-carbohydrate diets increase bone fragility through TGF-β–dependent control of osteocyte function
- Lipocalin-2 Regulates Osteocyte Ferroptosis and Osteocyte-Osteoblast Crosstalk via Wnt Signaling to Control Bone Formation
- Global Transcriptional Profiling of Adipose Tissue Uncovers Unique Sex-Dependent Mechanisms in Acute Obesity: Implications for Adipose-Heart Interorgan Crosstalk
- Fluid shear stress generates a unique signaling response by activating multiple TGFβ family type I receptors in osteocytes
- Mechanosensitive miR‐100 coordinates TGFβ and Wnt signaling in osteocytes during fluid shear stress
- Fluid shear stress generates a unique signaling response by activating multiple TGFβ family type I receptors in osteocytes
- Mechanosensitive miR‐100 coordinates TGFβ and Wnt signaling in osteocytes during fluid shear stress
- High-fat and high-carbohydrate diets increase bone fragility through TGF-β–dependent control of osteocyte function
- Osteocyte-Specific TGFβ Signaling Mitigates Obesity-Induced Deregulated Energy Metabolism and Compromised Bone Quality
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Age-related decline in osteocytic TGFβ signaling disrupts collagen integrity and bone quality
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Age-related decline in osteocytic TGFβ signaling disrupts collagen integrity and bone quality
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Age-related decline in osteocytic TGFβ signaling disrupts collagen integrity and bone quality
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Age-related decline in osteocytic TGFβ signaling disrupts collagen integrity and bone quality
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Age-related decline in osteocytic TGFβ signaling disrupts collagen integrity and bone quality
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Age-related decline in osteocytic TGFβ signaling disrupts collagen integrity and bone quality
- Aging impairs the osteocytic regulation of collagen integrity and bone quality
- Age-related decline in osteocytic TGFβ signaling disrupts collagen integrity and bone quality
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