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Biology subjects

Bilek, M. M.

Publications and source records attributed to Bilek, M. M..

2 recordsLinked to original sources

A Modular Microfluidic System to Generate Gradient Hydrogels with Simple-to-Complex Stiffness Profiles for Mechanobiology

Engineered stiffness gradient hydrogels offer exciting opportunities to probe fundamental mechanobiological processes in vitro. However, the need to spatially manipulate the properties of soft hydrogels at the micron scale poses challenges in developing fabrication platforms that can reliably modulate the gradient gel characteristics according to user needs. This study describes a modular approach leveraging thermophoresis in microfluidics to create high-fidelity stiffness gradients with linear and complex profiles, including periodic and anisotropic gradients. This study describes the platforms design and optimization, demonstrating achievable stiffness ranges and gradient slopes that correlate with many physiologic and diseased tissue types. This platform is also compatible with different hydrogel crosslinking chemistries, providing a versatile tool to engineer microenvironments with increased complexity. Directionally biased fibroblast cell proliferation and migration on fabricated stiffness gradient gelatin methacryloyl (GelMA) hydrogels indicate the effectiveness of this platform in modulating the mechanical microenvironment of cells. The results indicate that both the absolute stiffness range and the pattern of stiffness variation jointly affect cell behaviors. Considering its remarkable flexibility, the fabrication platform can significantly advance the development of biophysical gradient hydrogels that better replicate the intricacies of native tissues and help realize the next breakthroughs in mechanobiology.

bioengineering↗

Local activation of focal adhesion kinase orchestrates the positioning of presynaptic scaffold proteins and Ca2+ channel function to control glucose dependent insulin secretion.

A developing understanding suggests that spatial compartmentalisation of components the glucose stimulus-secretion pathway in pancreatic {beta} cells are critical in controlling insulin secretion. To investigate the mechanisms, we have developed live-cell sub-cellular imaging methods using the organotypic pancreatic slice. We demonstrate that the organotypic pancreatic slice, when compared with isolated islets, preserves intact {beta} cell structure, and enhances glucose dependent Ca2+ responses and insulin secretion. Using the slice technique, we have discovered the essential role of local activation of integrins and the downstream component, focal adhesion kinase, in regulating {beta} cells. Integrins and focal adhesion kinase are exclusively activated at the {beta} cell capillary interface and using in situ and in vitro models we show their activation both positions presynaptic scaffold proteins, like ELKS and liprin, and regulates glucose dependent Ca2+ responses and insulin secretion. We conclude that focal adhesion kinase orchestrates the final steps of glucose dependent insulin secretion within the restricted domain where {beta} cells contact the islet capillaries.

cell biology↗