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Design and analysis of a long‐term live‐cell imaging chamber for tracking cellular dynamics within cultured human islets of Langerhans
Author(s) -
Moogk Duane,
Hanley Stephen,
Ramunas John,
Blaylock April,
Skorepova Jana,
Rosenberg Lawrence,
Jervis Eric
Publication year - 2007
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.21335
Subject(s) - islet , live cell imaging , microbiology and biotechnology , cell , cell culture , biology , insulin , endocrinology , biochemistry , genetics
A means of expanding islet cell mass is urgently needed to supplement the limited availability of donor islets of Langerhans for transplant. Live cell imaging of human islets in culture has the potential to identify the specific cells and processes involved in islet expansion. A novel imaging chamber was developed to facilitate long‐term three‐dimensional imaging of human islets during transformation. Islets have been induced to transform into duct‐like epithelial cystic structures and revert back to glucose responsive endocrine cells under appropriate conditions (Jamal et al. Cell Death Differ. 2005 12:702–712). Here we aim to further our understanding by characterizing the process at a single cell level over time—essentially constructing a high resolution recorded history of each cell and its progeny during transformation and reversion. The imaging chamber enables high resolution imaging of three‐dimensional islets while maintaining the structure of the islet cells and intercellular matrix components. A mathematical model was developed to validate the imaging chamber design by determining the required chamber dimensions to avoid introduction of oxygen and nutrient transport limitations. Human islets were embedded in collagen in the imaging chamber and differential interference contrast time course images were obtained at 3 min intervals. Immunofluorescent imaging confirmed that islet phenotype was maintained for at least 5 days during imaging. Analysis of the time courses confirms our ability to identify and track individual cells over time and to observe cell death and phenotype transformation in isolated human islets. Biotechnol. Bioeng. 2007; 97: 1138–1147. © 2007 Wiley Periodicals, Inc.