Bone Biology and Disease:
Our Bone Biology and Disease program is focused on defining the signals and mechanisms important for bone formation and resorption in both normal and pathological situations (osteoporosis and osteopetrosis). While it is known that osteoblasts differentiate and localize the formation of new bone to regions where osteoclastic bone resorption has occurred, the signals responsible for this coupling effect are unknown and have become a focus of this research program. Another major research area in this program is centered on the pathophysiology of bone erosions in inflammatory arthritis, wear debris-induced osteolysis, which is responsible for aseptic loosening of orthopaedic implants, and bone infections, or osteomyelitis. We have also made major advances in understanding how environmental hazards/toxins, such as lead and smoke, can predispose individuals to bone loss or osteoporosis.
Cartilage Biology and Arthritis:
Our Cartilage Biology and Arthritis program investigates the mechanisms of chondrogenesis, chondrocyte maturation, and chondrocyte metabolism during normal skeletal growth and cartilage disease. A major emphasis of this program is geared toward using genetic and injury induced animal models to uncover the pathologic processes associated with inflammatory and non-inflammatory arthritis including: rheumatoid arthritis, psoriatic arthritis, lupus arthritis, and osteoarthritis. Our belief is that combining laboratory research with clinical investigation is the most effective way to bring better treatments to people affected by all types of arthritic disease.
Musculoskeletal Stem Cell Biology:
Our Musculoskeletal Stem Cell Biology program covers broad interests in the identification, self-renewal, maintenance, cell fate determination, and differentiation of several types of musculoskeletal stem cells. These include mesenchymal stem cells that give rise to cartilage, bone, fat, and connective tissues, hematopoietic stem cells that generate all blood cells and are housed in the bone marrow, and skeletal muscle stem cells that are required for skeletal muscle growth and regeneration. We study these stem cells both in the context of embryonic development and adult musculoskeletal repair and tissue engineering. We are attempting to gain a broader understanding of the molecular circuits that regulate stem cell self-renewal and differentiation so that we may develop strategies to manipulate musculoskeletal stem cells for treatments of congenital skeletal dysplasias, age-related skeletal diseases (osteoporosis and osteoarthritis), bone fractures, myelodysplasias, sarcopenia, neuromuscular degenerative disorders, and skeletal and hematopoietic related cancers
Program Faculty: Hani Awad, Danielle Benoit, Brendan Boyce, Laura Calvi, Joe Chakkalakal, Roman Eliseev,, Regis J. O’Keefe, J. Edward Puzas, Randy Rosier, Edward M. Schwarz, Lianping Xing, Xinping Zhang, Michael J. Zuscik
Musculoskeletal Repair and Maintenance:
In our Musculoskeletal Repair program, we perform translational studies designed to help understand common problems encountered by physicians when treating a wide array of musculoskeletal related injuries. Animal models of facture healing, structural bone grafting, distraction osteogenesis, skeletal muscle degeneration, skeletal muscle atrophy, and tendon injury have been developed to study repair mechanisms. Current applications of our animal models include: identifying mechanisms for enhanced musculoskeletal repair, devising cell-based tissue engineering, pharmacological and gene therapy approaches to enhance bone, tendon and skeletal muscle repair, regeneration or maintenance, and identifying cell-signaling pathways that control mesenchymal and skeletal muscle stem cell activation, expansion, and differentiation during bone, cartilage and skeletal muscle repair.
Our Musculoskeletal Development program is focused on identifying the mechanisms that underlie multiple aspects of axial and appendicular skeletal and skeletal muscle development including: patterning events, chondrogenesis, myogenesis, endochondral and intramembranous bone development, and joint formation. Developmental studies using genetic mouse models and primary cell culture techniques have identified multiple signaling molecules and transcription factors that are not only critical for normal musculoskeletal development, but are also implicated in congenital pediatric musculoskeletal disorders and adult musculoskeletal diseases.
Bone Cancer Biology:
Bone is a common site of breast and prostate cancer metastasis. It is also a site for the formation of primary tumors. In our Bone Cancer Biology program, we are studying the mechanisms of bone destruction following breast and prostate cancer metastasis and the regulation of malignant progression. Additional fields of active study include investigations into the mechanisms of radiation therapy resistance that is exhibited by cartilage and tumor cells and the survival vs. apoptotic processes of primary bone tumor cells.
- URMC Joins NIH Network Dedicated to Finding New Treatments for Rheumatoid Arthritis, Lupus
September 25, 2014
Announcement and Call for Abstracts
July 14, 2014
- For Scoliosis Patient, New Growing Rod Means Fewer Surgeries
June 11, 2014
- Better Tissue Healing with Disappearing Hydrogels
June 6, 2014
- Kates Installed as Inaugural Hansjorg Wyss Professor
April 2, 2014
- URMC Physician-Couple Gives $750K Gift to Orthopaedics
April 7, 2014
- Dr. Regis O'Keefe, MD, PhD Receives ORS/OREF 2014 Distinguished Investigator Award
April 2, 2014
- URMC's Elfar Honored with Hand Surgeon-Scientist Award
December 19, 2013
- Baumhauer Named One of North America's Top Foot and Ankle Surgeons
December 19, 2013
- Musculoskeletal Research Symposium A Huge Success
September 23, 2013
- $2M Gift to Support Geriatric Fracture Care, Orthopaedic Research
September 16, 2013
- URMC Orthopaedics Ranks No. 1 in Nation in NIH Funding
March 15, 2013
January 28, 2015
8:30 am - 9:30 am
Neuman Room (Rm 1-6823)
Maggie Thomas - Nanoparticle mediated Serpine1-siRNA treatment to prevent flexor tendon adhesions
Sarah Catheline - Coordinate dysregulation of SOX9 and RUNX2 during the development of osteoarthritis