Contact
Location
MEC Room 309
Lab
4040 Lewis and Clark Dr
122 Engineer's Way
Charlottesville, VA 22904

About

We are actively recruiting students and postdocs from all levels, please send your up-to-date transcript and CV for inquiry.

Adaptation of the structure at all levels of hierarchy. The main focus of Dr. Tang's lab is to understand how these structures relate to their biomechanical functions across multiple length scales, with a particular interest at micro- and nanoscale levels. This understanding is critically important as some musculoskeletal diseases originate at the fundamental building block levels of individual collagen fibrils and mineral particles, such as in spinal disc degeneraition and osteoarthritis.

By leveraging some of the most advanced imaging and characterization techniques, such as 3D volume electron tomography, correlative light and electron tomography, synchrotron X-ray scattering, and X-ray microscopy, and AI-driven image analysis, Dr. Tang's team aims to reveal some of the most complex biological tissue functions in bone, cartilage, tendon or related structures.

Before joining UVA, Dr. Tang was an Adjunct Professor and Research Associate in the Department of Materials Science and Engineering at McMaster University, Canada. She received her Ph.D. in Materials Engineering from the University of British Columbia, followed by post-doctoral training in the Department of Biomaterials at the Max Planck Institute of Colloids and Interfaces in Golm, Germany.

Education

Research Associate, Materials Science and Engineering, McMaster University

Post-doc, Biomaterials, Max Planck Institute of Colloids and Interfaces

Ph.D., Materials Engineering, University of British Columbia

B.Eng., Materials Science and Engineering, Huazhong University of Science and Technology

Research Interests

Biomechanics
Biomaterials
Structure-function relationships
Advanced microscopic imaging
Biomineralizing tissues
Bioimaging
Bone, Cartilage, Tendon

Selected Publications

Characterization of human trabecular bone across multiple length scales using a correlative approach combining X-ray tomography with LaserFIB and plasma FIB-SEM Tang, T.*, Casagrande, T., Moahmmadpour, P., Landis, W., Lievers, B., Grandfield, K.
Subcanalicular nanochannel volume is inversely correlated with calcium content in human cortical bone Tang, T., Landis, W., Blouin, S., Bertinetti, L., Hartmann, M., Berzlanovich, A., Weinkamer, R., Wagermaier, W., Fratzl, P.
A 3D network of nanochannels for possible ion and molecule transit in mineralizing bone and cartilage Tang, T., Landis, W., Raguin, E,. Werner, P,. Bertinetti, L., Dean, M., Wagermaier, W., Fratzl, P.
Breast cancer-secreted factors perturb murine bone growth in regions prone to metastasis Chiou, A., Chuang, L., Moreno, I., Tang, T., Wagermaier, W., Dean, M., Fischbach, C., Fratzl, P.
Three-dimensional structural interrelations between cells, extracellular matrix, and mineral in normally mineralizing avian leg tendon Zou, Z.*, Tang T.*, Macías-Sánchez, E., Sviben, S., Landis, W.J., Bertinetti, L., Fratzl, P.
Hypermineralization in the femoral neck of the elderly Tang, T., Wagermaier, W., Schuetz, R., Wang, Q., Eltit, F., Fratzl, P. and Wang, R.
Clinical hip fracture is accompanied by compression induced failure in the superior cortex of the femoral neck Tang, T., Cripton, P., Guy, P., McKay, H., and Wang, R.
Shear deformation and fracture of human cortical bone Tang, T., Ebacher, V., Guy, P., Cripton, P., McKay, H., and Wang, R.

Courses

Special Topics: Fracture Mechanics
Statics

Awards and Professional Service

Constance Livingstone-Friedman and Sydney Friedman Foundation Scholar
Die undesleistungsbesoldungsverordnung
ICCBMT Young Investigator Award
Bone Reports Early Career Researcher Editorial Board

Featured Grants & Projects

NSERC Discovery Grant – Individual Toward establishing novel interfacial materials characterization platforms
NSERC Alliance Catalyst Grant A novel 3D synergistic approach to characterize biology-structure-mechanics relationships in cranial sutures
CALM Project Seed Grant The architecture of bone osteocyte lacunocanalicular network in men with prostate cancer bone metastases
German Electron Synchrotron DESY Correlation between bone minerals and cell network at bone-cartilage interface: A high resolution SAXS/WAXS study
National Science Foundation Mechanisms of Stress Fracture in Human Femoral Neck through a Multiscale Approach This award supports research to uncover why some bones develop stress fractures while others, which look similar by standard clinical measures, do not. Stress fractures are small cracks that build up in bone under repeated loading, and are common during demanding physical training, such as that of athletes, first responders, and military service members. They occur far more often in women than in men, for reasons of physiology that remain unclear. This project tests the idea that the answer lies within the bone, in the fine structure and material quality of the tissue and in the cellular network that runs through it. Using human bone from the hip and imaging that spans from the whole bone to features far smaller than a cell, the research investigates where fatigue damage begins and what allows it to grow or stop. The work serves the national interest by advancing the national health, providing a scientific foundation for predicting, preventing, and treating these common injuries, and guiding the design of fatigue-resistant materials modeled on the multiscale architecture of bone. It also strengthens the engineering workforce through research training open to all interested students and shares its discoveries through public outreach.

This research advances biomechanics and mechanobiology by explaining how bone, as a hierarchical composite material, resists or accumulates fatigue damage. Its central premise is that whether a microscopic crack remains stable or grows into a stress fracture is governed by the local material quality of the bone and by its architecture, from mineral and collagen, to the cellular network that pervades the tissue, to features nanometers in size. The project first applies physiologically realistic cyclic loading to human hip bones from matched male and female donors and uses full-field optical strain measurement to locate where fatigue cracks form. It then resolves the finer scales: mineral content and distribution are quantified by electron microscopy imaging; fatigue cracks are reconstructed in three dimensions by high-resolution light microscopy and related directly to the surrounding cellular network; and crack interactions with the smallest features are imaged by high-resolution volume electron microscopy. By connecting whole-bone mechanics to tissue, cellular, and nanoscale structure, the project addresses a central question in biomechanics and mechanobiology: how biological architecture governs fatigue failure. The resulting framework also transfers to other mineralized tissues and to the design of fatigue-resistant engineered materials.