Development of a 3D bioprinted airway smooth muscle model for manipulating structure and measuring contraction

• Published in: bioRxiv
• Main Authors: Osagie, Jeffery O, Syeda, Sanjana S, Turner-Brannen, Emily, Guimond, Michelle, Parrenas, Lumiere C, Haroon, Ahsen, Imasuen, Philip, West, Adrian R
• Format: Paper
• Language: English
• Published: Cold Spring Harbor Cold Spring Harbor Laboratory Press 19.12.2022; Cold Spring Harbor Laboratory
• Edition: 1.2
• Subjects: Actin; Alginic acid; Collagen; Cytochalasin D; Extracellular matrix; Fibrinogen; Fibrosis; Lung diseases; Mechanical properties; Muscle contraction; Physiology; Potassium chloride; Respiratory tract; Smooth muscle; Tissue engineering; Webs; Relaxation; 3D bioprinting; Airway smooth muscle; Contraction; Mechanobiology
• ISSN: 2692-8205; 2692-8205
• DOI: 10.1101/2022.12.15.520464

The contractile function of airway smooth muscle (ASM) is inextricably linked to its mechanical properties and interaction with the surrounding mechanical environment. As tissue engineering approaches become more commonplace for studying lung biology, the inability to replicate realistic mechanical contexts for ASM will increasingly become a barrier to a fulsome understanding of lung health and disease. To address this knowledge gap, we describe the use of 3D bioprinting technology to generate a novel experimental model of ASM with a wide scope for modulating tissue mechanics. Using a stiffness modifiable alginate-collagen-fibrinogen bioink, we demonstrate that modulating the stiffness of free-floating ASM 'bare rings' is unfeasible; bioink conditions favorable for muscle formation produce structures that rapidly collapse. However, the creation of novel 'sandwich' and 'spiderweb' designs that encapsulate the ASM bundle within stiff acellular load bearing frames successfully created variable elastic loads opposing tissue collapse and contraction. Sandwich and spiderweb constructs demonstrated realistic actin filament organisation, generated significant baseline tone, and responded appropriately to acetylcholine, potassium chloride and cytochalasin D. Importantly, the two designs feasibly simulate different mechanical contexts within the lung. Specifically, the sandwich was relatively compliant and subject to plastic deformation under high contractile loads, whereas the stiffer spiderweb was more robust and only deformed minimally after repeated maximal contractions. Thus, our model represents a new paradigm for studying ASM contractile function in a realistic mechanical context. Moreover, it holds significant capacity to study the effects of ECM composition, multiple cell types and fibrosis on lung health and disease.Competing Interest StatementThe authors have declared no competing interest.