Constructing 3D voxelated tissues with molecular architecture encoded modular biomaterials to understand and control stem cell function

NIH RePORTER · NIH · R35 · $387,104 · view on reporter.nih.gov ↗

Abstract

PROJECT SUMMARY Most biological tissues are not simply static materials but active living composites. They are composed of living cells dispersed in nonliving polymers known as extracellular matrix. Decades of research in biomaterials have demonstrated a multitude of ways in which polymeric materials can influence cells, and cells can modify polymeric materials. Thus, recent advances in biomaterials design have shifted from pure elastic to viscoelastic polymeric biomaterials featuring time-dependent mechanical properties. However, existing biomaterial design largely relies on flexible linear polymers; such a simple molecular architecture intrinsically limits using linear polymers to create biomaterials with nonlinear elasticity and relaxation dynamics matching the complexity and variations in tissue-specific mechanics for dissecting intricate cell-matrix interactions. Moreover, there remains a grand challenge in assembling cells and soft, viscoelastic biomaterials to create tightly organized structures matching that of three-dimensional (3D) tissues for probing and exploiting cell-cell interactions. Trained as a theoretical polymer physicist but later switched to experimental soft (bio)materials and bioengineering, I have identified compelling opportunities for me to uniquely help address these challenges. Leveraging our expertise in polymer physics, polymer chemistry, and bioengineering, I will develop platform technologies for constructing voxelated 3D tissues with molecular architecture encoded modular biomaterials to understand and control stem cell function. This is based on two research areas that I have been pioneering: (1) bottlebrush polymers and networks and (2) voxelated bioprinting. In Thrust 1, I will develop modular bottlebrush gels to understand and control cell-matrix interactions. This thrust is built on my lab's recent breakthrough in discovering a new way to control the relaxation time without altering the shape of viscoelastic spectra of polymer networks. Leveraging my expertise in theoretical polymer physics and soft matter, and based on how cells interact with matrix, I will introduce two new sets of parameters to provide a more complete description of matrix strain-stiffening and viscoelasticity. Further, I will develop general strategies for independently encoding stiffness, strain-stiffening, relaxation time, and the shape of relaxation profile into the molecular architecture of bottlebrush gels. Using these modular bottlebrush gels, I will dissect the impact of each parameter on the behavior of stem cells. Recently, my lab proposed and showed the concept of voxelated bioprinting, a technology that enables precise manipulation and assembly of highly viscoelastic spheric bio-ink droplets in 3D space. In Thrust 2, I will advance our voxelated bioprinting technology to print multiple material voxels in which are encapsulated different types of cells. I hypothesize that pre-defining the specific location and cell-cell interac...

Key facts

NIH application ID
10939530
Project number
1R35GM154912-01
Recipient
UNIVERSITY OF VIRGINIA
Principal Investigator
Liheng Cai
Activity code
R35
Funding institute
NIH
Fiscal year
2024
Award amount
$387,104
Award type
1
Project period
2024-08-01 → 2029-07-31