TY - JOUR
T1 - Calcium phosphate cement chamber as an immunoisolative device for bioartificial pancreas
T2 - In vitro and preliminary in vivo study
AU - Yang, Kai Chiang
AU - Wu, Chang Chin
AU - Sumi, Shoichiro
AU - Tseng, Ching Li
AU - Wu, Yueh Hsiu Steven
AU - Kuo, Tzong Fu
AU - Lin, Feng Huei
PY - 2010/5
Y1 - 2010/5
N2 - Objectives: This study examined a calcium phosphate cement (CPC) chamber as an immunoisolative device to facilitate the use of xenogeneic cell sources without immunosuppression for the bioartificial pancreas (Bap). Methods: Mouse insulinoma cells were encapsulated in agarose gel and then enclosed in a CPC chamber to create a BAP. Bioartificial pancreas were evaluated by cell viability, live-dead cell ratio, and cytokine-mediated cytotoxicity assay and implanted into the peritoneal cavity of diabetic rats. Nonfasting blood glucose and serum insulin levels were analyzed perioperatively; BAPs were also retrieved for histological examination. Results: Insulinoma cells enclosed in the CPC chamber had normal viability, cell survival, and insulin secretion that was even cultured in media with cytokines. The nonfasting blood glucose level of rats was decreased from 460 ± 50 to 132 ± 43 mg/dL and maintained euglycemia for 22 days; serum insulin level was increased from 0.34 ± 0.11 to 1.43 ± 0.30 μg/dL after operation. Histological examination revealed the fibrous tissue envelopment, and immune-related cells that competed for oxygen resulting in hypoxia could be attributed to the dysfunction of BAPs. Conclusions: This study proved the feasibility for using a CPC chamber as an immunoisolative device for the BAP. An alternative implanted site should be considered to extend the functional longevity of BAPs in further study.
AB - Objectives: This study examined a calcium phosphate cement (CPC) chamber as an immunoisolative device to facilitate the use of xenogeneic cell sources without immunosuppression for the bioartificial pancreas (Bap). Methods: Mouse insulinoma cells were encapsulated in agarose gel and then enclosed in a CPC chamber to create a BAP. Bioartificial pancreas were evaluated by cell viability, live-dead cell ratio, and cytokine-mediated cytotoxicity assay and implanted into the peritoneal cavity of diabetic rats. Nonfasting blood glucose and serum insulin levels were analyzed perioperatively; BAPs were also retrieved for histological examination. Results: Insulinoma cells enclosed in the CPC chamber had normal viability, cell survival, and insulin secretion that was even cultured in media with cytokines. The nonfasting blood glucose level of rats was decreased from 460 ± 50 to 132 ± 43 mg/dL and maintained euglycemia for 22 days; serum insulin level was increased from 0.34 ± 0.11 to 1.43 ± 0.30 μg/dL after operation. Histological examination revealed the fibrous tissue envelopment, and immune-related cells that competed for oxygen resulting in hypoxia could be attributed to the dysfunction of BAPs. Conclusions: This study proved the feasibility for using a CPC chamber as an immunoisolative device for the BAP. An alternative implanted site should be considered to extend the functional longevity of BAPs in further study.
KW - Bioartificial pancreas
KW - Calcium phosphate cement
KW - Immunoisolation
KW - Xenotransplantation
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U2 - 10.1097/MPA.0b013e3181be2f95
DO - 10.1097/MPA.0b013e3181be2f95
M3 - Article
C2 - 20084047
AN - SCOPUS:77951720688
SN - 0885-3177
VL - 39
SP - 444
EP - 451
JO - Pancreas
JF - Pancreas
IS - 4
ER -