Abstract
Transplantation of hydrogel-encapsulated pancreatic islets is a promising long-term treatment for type 1 diabetes that restores blood glucose regulation while providing graft immunoprotection. Most human-scale islet encapsulation devices that rely solely on diffusion fail to provide sufficient surface area to meet islet oxygen demands. Perfused macroencapsulation devices use blood flow to mitigate oxygen limitations but increase the complexity of blood-device interactions. Here we describe a human-scale in vitro perfusion system to study hemocompatibility and performance of islet-like cell clusters (ILCs) in alginate hydrogel. A cylindrical perfusion device was designed for multi-day culture without leakage, contamination, or flow occlusion. Rat blood perfusion was assessed for prothrombin time and international normalized ratio and demonstrated no significant change in clotting time. Ex vivo perfusion performed with rats showed patency of the device for over 100 min using Doppler ultrasound imaging. PET-CT imaging of the device successfully visualized metabolically active mouse insulinoma 6 ILCs. ILCs cultured for 7 days under static conditions exhibited abnormal morphology and increased activated caspase-3 staining when compared with the perfused device. These findings reinforce the need for convective transport in macroencapsulation strategies and offer a robust and versatile in vitro system to better inform preclinical design.
Highlights
Type 1 diabetes is an autoimmune disease that selectively destroys the glucose-sensing, insulinsecreting islet beta cells
Patients are typically treated via frequent blood glucose monitoring and administration of exogenous insulin
The proposed system offers a way to accommodate thick cell-hydrogel constructs while establishing convective mass transport, which is currently lacking in the 3D cell culture field
Summary
Type 1 diabetes is an autoimmune disease that selectively destroys the glucose-sensing, insulinsecreting islet beta cells. Islet transplantation aims to provide long-term blood glucose sensing and regulation by replacing the missing beta cells. Current islet transplantation procedures require lifelong immunosuppression to minimize graft rejection, chronic rejection is not completely avoided (Korsgren et al, 2005; Gibly et al, 2011; McCall and Shapiro, 2012). Numerous micro- or macroencapsulation methods have been proposed to safely deliver the therapeutic cells while protecting them against host immune attack (Scharp and Marchetti, 2014; Moeun et al, 2019). Microencapsulation devices each contain one or a few islets (Scharp and Marchetti, 2014), while macroencapsulation approaches aim to deliver an entire therapeutic cell dose in one or a few devices
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