The association between in vivo physicochemical changes and inflammatory responses against alginate based microcapsules

被引:50
作者
de Vos, Paul [1 ]
Spasojevic, Milica [2 ]
de Haan, Barri
Faas, Marijke M.
机构
[1] Univ Med Ctr Groningen, Sect Immunoendocrinol, Dept Pathol & Med Biol, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Polymer Chem Lab, NL-9747 AG Groningen, Netherlands
关键词
Alginate; Bioartificial pancreas; Microencapsulation; XPS (X-ray photoelectron spectroscopy); Inflammation; L-LYSINE MICROCAPSULES; PANCREATIC-ISLET GRAFTS; PLL CAPSULES; MICROENCAPSULATED ISLETS; BIOCOMPATIBILITY; CHEMISTRY; CELLS; OVERGROWTH; POLYCATION; IMMUNOPROTECTION;
D O I
10.1016/j.biomaterials.2012.04.039
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Application of alginate-polylysine (PLL) capsules for immunoisolation of living cells are suffering from a varying degree of success and large lab-to-lab variations. In this study we show that these differences in success rates can be attributed to alginate dependent essential physicochemical changes of the properties of capsules in vivo that will render the capsules more susceptible to inflammatory responses. Capsule properties were studied before and after implantation by XPS, by immunocytochemistry, and by measuring zeta potentials. We studied a capsule type which provokes for unknown reasons a strong inflammatory response, i.e. high-guluronic (G) alginate capsules and a capsule type with near identical physicochemical properties but which evokes a minimal inflammatory response, i.e. intermediate-G alginate capsules. The cause of the difference in response was a decrease in nitrogen content on high-G capsules due to detachment of PLL in vivo and an increase of the zeta-potential. Our data illustrate an important overlooked phenomena: the physicochemical properties are not necessarily the properties after exposure to the in vivo microenvironment and might induce undesired inflammatory responses and failure of encapsulated cellular grafts. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5552 / 5559
页数:8
相关论文
共 61 条
[1]
Cytokines Tumor Necrosis Factor-α and Interferon-γ Induce Pancreatic β-Cell Apoptosis through STAT1-mediated Bim Protein Activation [J].
Barthson, Jenny ;
Germano, Carla M. ;
Moore, Fabrice ;
Maida, Adriano ;
Drucker, Daniel J. ;
Marchetti, Piero ;
Gysemans, Conny ;
Mathieu, Chantal ;
Nunez, Gabriel ;
Jurisicova, Andrea ;
Eizirik, Decio L. ;
Gurzov, Esteban N. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (45) :39632-39643
[2]
Optimized parameters for microencapsulation of pancreatic islet cells: an in vitro study clueing on islet graft immunoprotection in type 1 diabetes mellitus [J].
Basta, G ;
Sarchielli, P ;
Luca, G ;
Racanicchi, L ;
Nastruzzi, C ;
Guido, L ;
Mancuso, F ;
Macchiarulo, G ;
Calabrese, G ;
Brunetti, P ;
Calafiore, R .
TRANSPLANT IMMUNOLOGY, 2004, 13 (04) :289-296
[3]
Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts [J].
Basta, Giuseppe ;
Montanucci, Pia ;
Luca, Giovanni ;
Boselli, Carlo ;
Noya, Giuseppe ;
Barbaro, Barbara ;
Qi, Meirigeng ;
Kinzer, Katie P. ;
Oberholzer, Jose ;
Calafiore, Riccardo .
DIABETES CARE, 2011, 34 (11) :2406-2409
[4]
Immunoisolation of Pancreatic Islet Grafts with No Recipient's Immunosuppression: Actual and Future Perspectives [J].
Basta, Giuseppe ;
Calafiore, Riccardo .
CURRENT DIABETES REPORTS, 2011, 11 (05) :384-391
[5]
Deletion of the tissue response against alginate-pll capsules by temporary release of co-encapsulated steroids [J].
Bünger, CM ;
Tiefenbach, B ;
Jahnke, A ;
Gerlach, C ;
Freier, T ;
Schmitz, KP ;
Hopt, UT ;
Schareck, W ;
Klar, E ;
de Vos, P .
BIOMATERIALS, 2005, 26 (15) :2353-2360
[6]
Grafts of microencapsulated pancreatic islet cells for the therapy of diabetes mellitus in non-immunosuppressed animals [J].
Calafiore, R ;
Basta, G ;
Luca, G ;
Calvitti, M ;
Calabrese, G ;
Racanicchi, L ;
Macchiarulo, G ;
Mancuso, F ;
Guido, L ;
Brunetti, P .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2004, 39 :159-164
[7]
Microcapsules and their ability to protect islets against cytokine-mediated dysfunction [J].
de Groot, M ;
Keizer, PPM ;
de Haan, BJ ;
Schuurs, TA ;
Leuvenink, HGD ;
van Schilfgaarde, R ;
de Vos, P .
TRANSPLANTATION PROCEEDINGS, 2001, 33 (1-2) :1711-1712
[8]
Structural surface changes and inflammatory responses against alginate-based microcapsules after exposure to human peritoneal fluid [J].
de Haan, Bart J. ;
Rossi, Alessandra ;
Faas, Marijke M. ;
Smelt, Maaike J. ;
Sonvico, Fabio ;
Colombo, Paolo ;
de Vos, Paul .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2011, 98A (03) :394-403
[9]
Factors influencing insulin secretion from encapsulated islets [J].
de Haan, BJ ;
Faas, MM ;
de Vos, P .
CELL TRANSPLANTATION, 2003, 12 (06) :617-625
[10]
Processing of immunoisolated pancreatic islets. Implications for histological analyses of hydrated tissue [J].
De Haan, BJ ;
van Goor, H ;
De Vos, P .
BIOTECHNIQUES, 2002, 32 (03) :612-+