| Literature DB >> 33895491 |
Jorge Santini-González1, Jennifer A Simonovich1, Roberto Castro-Gutiérrez2, Yarelis González-Vargas3, Nicholas J Abuid1, Cherie L Stabler1, Holger A Russ2, Edward A Phelps4.
Abstract
The peri-islet extracellular matrix (ECM) is a key component of the microenvironmental niche surrounding pancreatic islets of Langerhans. The cell anchorage and signaling provided by the peri-islet ECM is critical for optimum beta cell glucose responsiveness, but islets lose this important native ECM when isolated for transplantation or in vitro studies. Here, we established a method to construct a peri-islet ECM on the surfaces of isolated rat and human islets by the co-assembly from solution of laminin, nidogen and collagen IV proteins. Successful deposition of contiguous peri-islet ECM networks was confirmed by immunofluorescence, western blot, and transmission electron microscopy. The ECM coatings were disrupted when assembly occurred in Ca2+/Mg2+-free conditions. As laminin network polymerization is divalent cation dependent, our data are consistent with receptor-driven ordered ECM network formation rather than passive protein adsorption. To further illustrate the utility of ECM coatings, we employed stem cell derived beta-like cell clusters (sBCs) as a renewable source of functional beta cells for cell replacement therapy. We observe that sBC pseudo-islets lack an endogenous peri-islet ECM, but successfully applied our approach to construct a de novo ECM coating on the surfaces of sBCs.Entities:
Keywords: Basement membrane; Extracellular matrix; Laminin-nidogen-collagen IV; Pancreatic islet; Stem cell-derived beta cell; Type 1 diabetes
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Year: 2021 PMID: 33895491 PMCID: PMC8131001 DOI: 10.1016/j.biomaterials.2021.120808
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 15.304