Shape-Preserved Transformation of Biological Cells into Synthetic Hydrogel Microparticles.
Kristin C MeyerNicholas R LabriolaEric M DarlingBryan KaehrPublished in: Advanced biosystems (2019)
The synthesis of materials that can mimic the mechanical, and ultimately functional, properties of biological cells can broadly impact the development of biomimetic materials, as well as engineered tissues and therapeutics. Yet, it is challenging to synthesize, for example, microparticles that share both the anisotropic shapes and the elastic properties of living cells. Here, a cell-directed route to replicate cellular structures into synthetic hydrogels such as polyethylene glycol (PEG) is described. First, the internal and external surfaces of chemically fixed cells are replicated in a conformal layer of silica using a sol-gel process. The template is subsequently removed to render shape-preserved, mesoporous silica replicas. Infiltration and cross-linking of PEG precursors and dissolution of the silica result in a soft hydrogel replica of the cellular template as demonstrated using erythrocytes, HeLa, and neuronal cultured cells. The elastic modulus can be tuned over an order of magnitude (≈10-100 kPa) though with a high degree of variability. Furthermore, synthesis without removing the biotemplate results in stimuli-responsive particles that swell/deswell in response to environmental cues. Overall, this work provides a foundation to develop soft particles with nearly limitless architectural complexity derived from dynamic biological templates.
Keyphrases
- induced apoptosis
- cell cycle arrest
- drug delivery
- living cells
- cell death
- endoplasmic reticulum stress
- signaling pathway
- gene expression
- pi k akt
- small molecule
- high resolution
- bone marrow
- mass spectrometry
- cell proliferation
- molecular dynamics simulations
- cell therapy
- wound healing
- extracellular matrix
- simultaneous determination
- life cycle