Juan M Taboas

Juan M Taboas

Contact

412-624-3391
408 Salk Pavilion
Administrative Assistant
Michele Leahy
412-648-3903
mmp2@pitt.edu

BS, MS, PhD

Assistant Professor

Biography

Dr. Taboas’ expertise is in skeletal tissue regeneration, stem cell mechanobiology, tissue engineering scaffolds, microfluidics devices, and real-time live-cell microscopy based functional bioassays. His laboratory develops approaches to regenerate cartilaginous interfacial tissues. These include the physis (epiphyseal growth plate), the mandibular condyle fibrocartilage, tendon and ligament insertion sites (entheses), the tide mark in articular cartilage, and the vertebral endplates. Cartilaginous interfaces share a common architectural feature: spatially discrete but proximate populations of chondrocytes at distinct states of differentiation. The physis is the cartilaginous interfacial tissue at the ends of limb bones that drives appendicular skeletal growth. No clinical approach exists to restore growth at the physis; it is a good model for cartilaginous interface tissue regeneration because it has chondrocytes at all stages of endochondral ossification, a process of coordinated cellular progression through all states with progenitors supplying new cells into the cycle at one end. The laboratory also collaborates with several PIs in the CCR to regenerate other skeletal and craniofacial tissues. Current research interests:

  1. Physeal regeneration in juveniles, to treat growth plate injury (tethers, osteosarcoma), skeletal dysplasia and complex bone injury.
  2. Physeal fracture repair in juveniles, tissue glue to promote proper healing
  3. Dental pulp regeneration in juveniles, injectable biomaterial to recruit stem cells and guide vital tissue formation (collaboration with Drs. Beniash, Ray and Sfeir)
  4. Extremity regeneration in adults, bone engineering in compromised wounds (e.g. blast injury, open fractures, collaboration with Drs. Almarza, Davis and Wang)
  5. Microtissue fabrication, for drug screening and therapy development. Can be cultured in custom microfluidic bioreactors design in house.

The laboratory employs novel hydrogel scaffolds, cell micro-patterning, custom microfluidic bioreactors, and real-time microscopy to study how the microenvironment modulates intracellular signaling, cell-cell communication, and tissue patterning and growth. These results are applied to the laboratory's tissue engineering approaches.

Education

University of Miami, BS 1993
Stanford University, MS 1995
University of Michigan, MS 2003
University of Michigan, MS 2003
University of Michigan, PhD 2004

Awards

  • K01 Research Scientist Developmental Award, NIAMS, NIH

Resources

Clinical Department

Oral Biology

Academic Department

Oral Biology

Departments