Enhanced Oxygen Supply Improves Islet Viability in a New Bioartificial Pancreas

被引:141
作者
Barkai, Uriel [1 ]
Weir, Gordon C. [2 ]
Colton, Clark K. [3 ]
Ludwig, Barbara [4 ]
Bornstein, Stefan R. [4 ]
Brendel, Mathias D. [4 ]
Neufeld, Tova [1 ]
Bremer, Chezi [1 ]
Leon, Assaf [1 ]
Evron, Yoav [1 ]
Yavriyants, Karina [1 ]
Azarov, Dimitri [1 ]
Zimermann, Baruch [1 ]
Maimon, Shiri [1 ]
Shabtay, Noa [1 ]
Balyura, Maria [1 ]
Rozenshtein, Tania [1 ]
Vardi, Pnina [5 ]
Bloch, Konstantin [6 ]
de Vos, Paul [7 ]
Rotem, Avi [1 ]
机构
[1] Beta O2 Technol, IL-49511 Kiryat Arie, Petach Tikva, Israel
[2] Joslin Diabet Ctr, Div Res, Sect Islet Transplantat & Cell Biol, Boston, MA 02215 USA
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[4] Univ Hosp Carl Gustav Carus, Dept Med 3, Dresden, Germany
[5] Lin Med Ctr, Dept Diabet, Clalit Hlth Serv, Haifa, Israel
[6] Tel Aviv Univ, Sackler Fac Med, Felsenstein Med Res Ctr, Diabet & Obes Res Lab, Petah Tiqwa, Israel
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Lab Med, Sect Immunoendocrinol, NL-9713 AV Groningen, Netherlands
关键词
Diabetes; Bioartificial pancreas (BAP); Islets; Implantation; Immune barrier; Oxygen; INSULIN-SECRETION; TRANSPLANTATION; RAT; ENCAPSULATION; SURVIVAL; CELLS; VASCULARIZATION; CONSUMPTION; DIFFUSION; APOPTOSIS;
D O I
10.3727/096368912X657341
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
The current epidemic of diabetes with its overwhelming burden on our healthcare system requires better therapeutic strategies. Here we present a promising novel approach for a curative strategy that may be accessible for all insulin-dependent diabetes patients. We designed a subcutaneous implantable bioartificial pancreas (BAP)-the "beta-Air" that is able to overcome critical challenges in current clinical islet transplantation protocols: adequate oxygen supply to the graft and protection of donor islets against the host immune system. The system consists of islets of Langerhans immobilized in an alginate hydrogel, a gas chamber, a gas permeable membrane, an external membrane, and a mechanical support. The minimally invasive implantable device, refueled with oxygen via subdermally implanted access ports, completely normalized diabetic indicators of glycemic control (blood glucose intravenous glucose tolerance test and HbA1c) in streptozotocin-induced diabetic rats for periods up to 6 months. The functionality of the device was dependent on oxygen supply to the device as the grafts failed when oxygen supply was ceased. In addition, we showed that the device is immuno-protective as it allowed for survival of not only isografts but also of allografts. Histological examination of the explanted devices demonstrated morphologically and functionally intact islets; the surrounding tissue was without signs of inflammation and showed visual evidence of vasculature at the site of implantation. Further increase in islets loading density will justify the translation of the system to clinical trials, opening up the potential for a novel approach in diabetes therapy.
引用
收藏
页码:1463 / 1476
页数:14
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