Abstract
This study investigates the effect of alginate/poly-l-lysine/alginate (APA) encapsulation on the insulin secretion dynamics exhibited by an encapsulated cell system. Experiments were performed with the aid of a home-built perfusion apparatus providing a 1 min temporal resolution. Insulin profiles were measured from: (i) murine insulinoma βTC3 cells encapsulated in calcium alginate/poly-l-lysine/alginate (APA) beads generated with high guluronic (G) or high mannuoric (M) content alginate, and (ii) murine insulinoma βTC-tet cells encapsulated in high M APA beads and propagated in the presence and absence of tetracycline. Results show that encapsulation in APA beads did not affect the insulin secretion profile shortly post-encapsulation. However, remodeling of the beads due to cell proliferation affected the insulin secretion profiles; and inhibiting remodeling by suppressing cell growth preserved the secretion profile. The implications of these findings regarding the in vivo function of encapsulated insulin secreting cells are discussed.
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Acknowledgements
This work was supported by funding from NIH (DK 56980) through a subcontract to Georgia Tech, as well as from the Georgia Tech/Emory Center (GTEC) for the Engineering of Living Tissues, an ERC Program of the National Science Foundation under Award Number EEC-9731643. This financial support is greatly appreciated. Additionally, the authors thank Dr. S. Efrat for providing the βTC3 and βTC-tet cells and Tracey Couse for help with histology.
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Cheng, SY., Constantinidis, I. & Sambanis, A. Insulin secretion dynamics of free and alginate-encapsulated insulinoma cells. Cytotechnology 51, 159–170 (2006). https://doi.org/10.1007/s10616-006-9025-4
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DOI: https://doi.org/10.1007/s10616-006-9025-4