School of Dentistry
Dr. Bumann received her B.S. in Anthropology/Zoology and D.D.S. from the University of Michigan in 2004 and 2008, respectfully. She subsequently received her Ph.D. in Oral and Craniofacial Sciences from the University of California, San Francisco in 2013. She conducted post-doctoral training in craniofacial biology and completed her residency and M.S. in pediatric dentistry at the University of Michigan. Part of her Ph.D. and all of her post-doctoral training were funded by a National Institutes of Health/National Institute of Dental and Craniofacial Research (NIH/NIDCR) K08 and L40 Pediatric Research Loan Repayment Program (LRP). She joined the Department of Oral and Craniofacial Sciences in the University of Missouri Kansas City (UMKC) School of Dentistry as an Assistant Professor in September 2017 where she is a member of the Center of Excellence in the Study of Dental and Musculoskeletal Tissues (CEMT) and the Doctoral Faculty. She is a member of the American Dental Association (ADA), the International and American Associations for Dental Research (IADR/AADR), American Dental Education Association (ADEA), International Association of Student Clinicians-American Dental Association (SCADA), American Society for Bone and Mineral Research (ASBMR), Society for Developmental Biology (SDB), American Association of Anatomists (AAA), and American Association of Pediatric Dentistry (AAPD). She currently serves on the Edward H. Hatton Awards Committee for AADR, the Constitution Committee for IADR, and as an External Advisory Board Member for the Comprehensive Training in Oral and Craniofacial Sciences Program (T32) at Ohio State University. Additionally, Dr. Bumann is currently licensed as a Pediatric Dentist in the state of Missouri.
Identified multiple developmental mechanisms that control the size and shape of the jaw skeleton. Our experiments not only reveal that neural crest mesenchyme (NCM) autonomously regulates cell cycle progression and the timing of osteogenic differentiation, but they also indicate that cell cycle and osteogenesis are inexorably linked as a developmental module in vivo as they are in vitro. Our work also uncovered a novel function for bone resorption, which is to help establish species-specific jaw length; and our transplant experiments indicate that the underlying molecular mechanisms stem from the ability of NCM to control the activity of its own derivatives (i.e., osteocytes) and also that of mesoderm-derived osteoclasts. We show the remarkable ability of NCM to maintain spatiotemporal control over the induction, differentiation, deposition, mineralization, and the resorption of bone is what integrates the determinants of jaw length across multiple embryonic stages, and is what empowers NCM with its ability to generate skeletal variation during disease and evolution.
Created a novel strategy for estimating species-specific contributions in chimeras and xenografts. We developed a simple molecular strategy to quantify species-specific contributions in chimeras and xenografts. Many tissue-engineering approaches for repair and regeneration involve transplants between species. Yet a challenge was to distinguish donor versus host effects on gene expression. We designed species-specific primers for reverse transcription quantitative real-time PCR (RT-qPCR) by identifying silent mutations in quail, duck, chicken, mouse and human ribosomal protein L19. This strategy enables chimeras and/or xenografts to be screened rapidly at the molecular level.
Demonstrated a molecular mechanism and clinical significance of calciotropic hormones in the regulation of mineralized tissue growth in the craniofacial skeleton. We investigated the role of AP-1 family members in the action of parathyroid hormone related protein (PTHrP) was examined in cementoblasts. PTHrP increased mRNA and protein levels of all Fos members, but only one Jun member (JunB) was increased. Overexpression of JunB in cementoblasts mimicked actions of PTHrP to support osteoclastogenesis and inhibit cementoblast differentiation, suggesting that the actions of PTHrP on mesenchymal cells operate through JunB. Additionally, we observed changes in the oral cavity observed in patients with primary hyperparathyroidism (HPT). We found both a decreased cortical density and an increased likelihood of oral tori. The contemporary oral manifestations of primary HPT are different from those previously reported, and health care providers should be aware of newer, more subtle findings that may be present when treating patients with HPT.
Recent Publications (More articles at PubMed)
1. Janice E Berry, Erin L Ealba, Glenda J Pettway, Nabanita S Datta, Erica C Swanson, Martha J Somerman, and Laurie K McCauley. JunB as a Downstream Mediator of PTHrP Actions in Cementoblasts. Journal of Bone and Mineral Research, 21(2):246-57. 2006 PMID: 16418780
2. Allan D. Padbury, Jr., Tolga F. Tozum, Mario Taba, Jr., Erin L. Ealba, Brady T. West, Richard E. Burney, Paul G. Gauger, William V. Giannobile, and Laurie K. McCauley. The Impact of Primary Hyperparathyroidism on the Oral Cavity. Journal of Clinical Endocrinology and Metabolism, 91(9):3439-45. 2006 PMID: 16822829
3. Roger, J. M., J. A. Javarone, E. L. Ealba, M. R. Markiewicz, and A. B. Morlandt. The National Student Research Group of the AADR—an introduction. Journal of Dental Research 86 (5):388-91. 2007 PMID:17452556
4. Ealba, E. L. and R. A. Schneider. A simple PCR-based strategy for estimating species-specific contributions in chimeras and xengografts. Development 140, 3062-3068. 2013 PMID: 23785056
5. Yu, J., A. H. Jheon, E. L. Ealba, B. F. Eames, K. D. Butcher, S. S. Mak, R. Ladher, T. Alliston, and R. A. Schneider. Evolution of a developmental mechanism: Species-specific regulation of the cell cycle and the timing of events during craniofacial osteogenesis. Developmental Biology 385(2):380-95. 2014 PMID: 24262986
6. Ealba, E. L., A. H. Jheon, J. Hall, C. Curantz, K. Butcher, and R. A. Schneider. Neural crest-mediated bone resorption is a determinant of species-specific jaw length. Developmental Biology 408:151-163. 2015 PMID: 26449912
7. Bumann, E. E. and Frazier-Bowers, S. A. A New Cyte of Orthodontic Tooth Movement. Orthodontics and Craniofacial Research Suppl 1: 125-128. 2017. PMID: 28643925
1. Bumann, E.E. and V. Kaartinen. Craniofacial Morphogenesis, Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism, 9th Edition, Section Editor, Laurie McCauley, Wiley-Blackwell.
Continuing Education Program
1. Bumann, E.E. Electrical Oral Burns, Practical Reviews in Pediatric Dentistry, Coordinating Editor, Arthur Nowak, Oakstone Publishing.
Dr. Erin Ealba Bumann (firstname.lastname@example.org)
Maria Gonzalez (email@example.com)