Physiomimetic Fluidic Culture Platform on Microwell-Patterned Porous Collagen Scaffold for Human Pancreatic Islets

Author:

Kato Hiroyuki1ORCID,Chen Huajian2,Shang Kuang-Ming3,Izumi Kenji4,Koba Naoya4,Tsuchiya Takanori4,Kawazoe Naoki2,Quijano Janine1,Omori Keiko1,Orr Chris1ORCID,Qi Meirigeng1,Ku Hsun Teresa1,Kandeel Fouad1,Tai Yu-Chong3,Chen Guoping2,Komatsu Hirotake1ORCID

Affiliation:

1. Department of Translational Research & Cellular Therapeutics, Arthur Riggs Diabetes & Metabolism Research Institute, City of Hope, Duarte, CA, USA

2. Research Center for Functional Materials, National Institute for Materials Science, Tsukuba, Japan

3. Department of Medical Engineering, California Institute of Technology, Pasadena, CA, USA

4. Tokai Hit, Fujinomiya, Japan

Abstract

Pancreatic islet transplantation is one of the clinical options for certain types of diabetes. However, difficulty in maintaining islets prior to transplantation limits the clinical expansion of islet transplantations. Our study introduces a dynamic culture platform developed specifically for primary human islets by mimicking the physiological microenvironment, including tissue fluidics and extracellular matrix support. We engineered the dynamic culture system by incorporating our distinctive microwell-patterned porous collagen scaffolds for loading isolated human islets, enabling vertical medium flow through the scaffolds. The dynamic culture system featured four 12 mm diameter islet culture chambers, each capable of accommodating 500 islet equivalents (IEQ) per chamber. This configuration calculates > five-fold higher seeding density than the conventional islet culture in flasks prior to the clinical transplantations (442 vs 86 IEQ/cm2). We tested our culture platform with three separate batches of human islets isolated from deceased donors for an extended period of 2 weeks, exceeding the limits of conventional culture methods for preserving islet quality. Static cultures served as controls. The computational simulation revealed that the dynamic culture reduced the islet volume exposed to the lethal hypoxia (< 10 mmHg) to ~1/3 of the static culture. Dynamic culture ameliorated the morphological islet degradation in long-term culture and maintained islet viability, with reduced expressions of hypoxia markers. Furthermore, dynamic culture maintained the islet metabolism and insulin-secreting function over static culture in a long-term culture. Collectively, the physiological microenvironment-mimetic culture platform supported the viability and quality of isolated human islets at high-seeding density. Such a platform has a high potential for broad applications in cell therapies and tissue engineering, including extended islet culture prior to clinical islet transplantations and extended culture of stem cell-derived islets for maturation.

Funder

National Institutes of Health

Japan Society for the Promotion of Science

Nora Eccles Treadwell Foundation

JDRF

National Cancer Institute of the National Institutes of Health

Publisher

SAGE Publications

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