Elizabeth K. Vu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Elizabeth K. Vu has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
- Elizabeth W. Bradley
Stem Cell Institute, University of Minnesota
2 shared publications - Emily Chavez
Department of Orthopedic Surgery, Medical School, University of Minnesota, Minneapolis, MN 55455, USA
2 shared publications - Grant Kim
Department of Orthopedic Surgery, Medical School, University of Minnesota, Minneapolis, MN 55455, USA
2 shared publications - Ismael Y. Karkache
Department of Orthopedic Surgery, Medical School, University of Minnesota, Minneapolis, MN 55455, USA
2 shared publications - Jinsha Koroth
Department of Orthopedic Surgery, Medical School, University of Minnesota, Minneapolis, MN 55455, USA
2 shared publications - Mitchell J. Shimak
Department of Orthopedic Surgery, Medical School, University of Minnesota, Minneapolis, MN 55455, USA
2 shared publications
Latest Publications
- Open Access
- 31 October 2025
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 26 (21) , 10619
From Development, Disease, and Decline: A Review of What Defines an Osteoclast Progenitor
Our understanding of the different developmental origins of osteoclast progenitors and their respective roles during homeostatic bone remodeling at different skeletal sites as well as their roles within bone regeneration and degenerative conditions is evolving. In this narrative review article, we summarize what is known about the developmental origins, anatomical sources, and markers of osteoclast progenitors. We touch on how osteoclast progenitors vary during different disease contexts, including periodontitis, rheumatoid arthritis, and osteoarthritis. In addition, we also characterize osteoclast progenitors that contribute to bone healing and define changes observed with advancing age. In this regard, we offer a critical review of gaps within our understanding and opportunities for future development within the field. Because of their diverse nature under different contexts, identifying and characterizing osteoclast progenitors may help to advance condition-specific therapies.
- 31 October 2025
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 26 (21) , 10619
Open AccessFrom Development, Disease, and Decline: A Review of What Defines an Osteoclast Progenitor
Our understanding of the different developmental origins of osteoclast progenitors and their respective roles during homeostatic bone remodeling at different skeletal sites as well as their roles within bone regeneration and degenerative conditions is evolving. In this narrative review article, we summarize what is known about the developmental origins, anatomical sources, and markers of osteoclast progenitors. We touch on how osteoclast progenitors vary during different disease contexts, including periodontitis, rheumatoid arthritis, and osteoarthritis. In addition, we also characterize osteoclast progenitors that contribute to bone healing and define changes observed with advancing age. In this regard, we offer a critical review of gaps within our understanding and opportunities for future development within the field. Because of their diverse nature under different contexts, identifying and characterizing osteoclast progenitors may help to advance condition-specific therapies.
- Open Access
- 14 February 2025
- Published by MDPI AG in Endocrines
- Vol. 6 (1) , 9
Induction of Mandibular Cortical Bone Defects to Study Bone Regeneration
Background/Objectives: In contrast to endochondral bone healing, the process of intramembranous bone regeneration is poorly understood. This limits our ability to repair and regenerate the craniofacial skeleton to either correct deformity or optimally heal tissues following injury. While there are several preclinical models of intramembranous regeneration within the craniofacial skeleton, some are not load bearing and others are technically challenging. The goal of this pilot study is therefore to describe a simple method for induction of cortical defects within the mandible that does not involve compounding injury to the surrounding tissues. Methods: Single cortex defects were generated in the mandible body of 8-week-old male and female mice. The extent of bone regeneration within the defect was characterized at days 0, 3, 14, and 28 following defect generation via micro-computed tomography and histology. Conclusions: Observed healing was predictable and reproducible and resulted in intramembranous bone formation. This model will help aid the understanding of intramembranous bone healing in load bearing bones (e.g., mandible) within the craniofacial skeleton
- 14 February 2025
- Published by MDPI AG in Endocrines
- Vol. 6 (1) , 9
Open AccessInduction of Mandibular Cortical Bone Defects to Study Bone Regeneration
Background/Objectives: In contrast to endochondral bone healing, the process of intramembranous bone regeneration is poorly understood. This limits our ability to repair and regenerate the craniofacial skeleton to either correct deformity or optimally heal tissues following injury. While there are several preclinical models of intramembranous regeneration within the craniofacial skeleton, some are not load bearing and others are technically challenging. The goal of this pilot study is therefore to describe a simple method for induction of cortical defects within the mandible that does not involve compounding injury to the surrounding tissues. Methods: Single cortex defects were generated in the mandible body of 8-week-old male and female mice. The extent of bone regeneration within the defect was characterized at days 0, 3, 14, and 28 following defect generation via micro-computed tomography and histology. Conclusions: Observed healing was predictable and reproducible and resulted in intramembranous bone formation. This model will help aid the understanding of intramembranous bone healing in load bearing bones (e.g., mandible) within the craniofacial skeleton