Active and passive crosslinking of cytoskeleton scaffolds tune the effects of cell inclusions on composite structure

TL;DR

This study develops a dynamic biomaterial scaffold embedding bacteria within cytoskeletal networks, demonstrating how passive and active crosslinking influence cell entrapment, network structure, and potential for autonomous material control.

Contribution

It introduces a novel composite scaffold with embedded bacteria and elucidates how different crosslinking methods affect its structural and functional properties.

Findings

Both passive and active crosslinking promote cell entrapment.

Depletion interactions are significant in uncrosslinked networks.

Large-scale structures form at low cell fractions without altering microscale structure.

Abstract

Incorporating cells within active biomaterial scaffolds is a promising strategy to develop forefront materials that can autonomously sense, respond, and alter the scaffold in response to environmental cues or internal cell circuitry. Using dynamic biocompatible scaffolds that can self-alter their properties via crosslinking and motor-driven force-generation opens even greater avenues for actuation and control. However, the design principles associated with engineering active scaffolds embedded with cells are not well established. To address this challenge, we design a dynamic scaffold material of bacteria cells embedded within a composite cytoskeletal network of actin and microtubules that can be passively or actively crosslinked by either biotin-streptavidin or multimeric kinesin motors. Using quantitative microscopy, we demonstrate the ability to embed cells of volume fractions 0.4 to 2% throughout the network without compromising the structural integrity of the network or inhibiting crosslinking or motor-driven dynamics. Our findings suggest that both passive and active crosslinking promote entrainment of cells within the network, while depletion interactions play a more important role in uncrosslinked networks. Moreover, we show that large-scale structures emerge with the addition of cell fractions as low as 0.4%, but these structures do not influence the microscale structural lengthscale of the materials. Our work highlights the potential of our composite biomaterial in designing autonomous materials controlled by cells, and provides a roadmap for effectively coupling cells to complex composite materials with an eye towards using cells as in situ factories to program material modifications.