• Skip to main content
  • Skip to primary navigation
Header Search Widget
site logo

O'Connell Lab

  • Research
    • Intervertebral disc tissue-level mechanics
    • Intervertebral disc joint-level mechanics
    • Computational modeling
    • Tissue engineering
    • Machine learning for in vivo soft tissue strain prediction
    • 3D printing/biomimetic composites
    • Machine learning- and sensor-based posture recognition
  • People
  • Publications
    • Journal Articles
    • Conference Proceedings
    • Master’s Reports
    • Undergraduate Independent Research
  • News
  • Blog
  • Photos
  • About
    • Teaching
    • Community
    • Industry
    • Funding
  • Resources
  • Intervertebral disc tissue-level mechanics
  • Intervertebral disc joint-level mechanics
  • Computational modeling
  • Tissue engineering
  • Machine learning for in vivo soft tissue strain prediction
  • 3D printing/biomimetic composites
  • Machine learning- and sensor-based posture recognition

Tissue engineering

Cartilage Tissue Engineering

Tissue engineering techniques use a combination of cells, scaffolds, and stimulating biochemical factors with the aim of creating engineered tissue constructs to replace diseased/damaged tissue and restore tissue function. A major set-back of cartilage tissue engineering strategies that use autologous chondrocytes is the loss of chondrogenic phenotype during two-dimensional (2D) expansion, a process that is essential for obtaining enough cells for three-dimensional (3D) tissue culture. Furthermore, there is currently no way to predict which cell sources are capable of producing sufficient matrix to create functional engineered tissue prior to the long, resource-intensive 3D culture process. To overcome this shortcoming, work in our lab is investigating the relationship between cellular properties during 2D expansion and 3D tissue production, a result which will have a transformative impact on biological repair strategies.

β-tubulin (red), f-actin stress fibers (green), and nuclei (blue) are imaged using immunofluorescence microscopy in passage two juvenile bovine chondrocytes.

If you are interested in the most recent updates of this project, please feel free to contact Emily Lindberg (emily_lindberg at berkeley dot edu)

Data from paper titled “Growth Factor Priming During Expansion Culture Increases Chondrogenic Tissue Production from Human Articular Chondrocytes”:  Human Paper Data

Hydrogel Mechanics Characterization

Additionally, native tissues and tissue interfaces represent composite materials with complex mechanical behaviors. Hydrogels can be used as scaffolds to investigate the effects of different components present in native and engineered tissues on mechanical properties. Currently, our laboratory is looking at how the addition of naturally present components like Collagen Type I affects the compressive and tensile mechanical properties of common hydrogels used for tissue engineering.

Agarose-alginate gel interfaces with collagen-infused gel

The addition of collagen affects compressive mechanical properties in cylindrical constructs.

If you are interested in the most recent updates of this project, please feel free to contact Gabriel Lopez (gabriel_lopezmarcial at berkeley dot edu)

Spine On A Chip

With cells embedded on bendable microfluidic silicone devices called organ-chips, components of the intervertebral disc can be grown while subjected to similar loading modalities found in the flexing spine. In this way, tissue modeling is accomplished experimentally by an interdisciplinary team at the Berkeley Biomechanics Laboratory in order to investigate questions fundamental to the health of our spines.

Prototyping the novel flexing Spine-on-a-chip (please click on this image for a brief YouTube Spine-on-a-chip video!)

 

  • Berkeley Engineering
  • UC Berkeley
  • youtube
  • X
  • Privacy
  • Accessibility
  • Nondiscrimination

© 2016–2025 UC Regents   |   Log in