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A novel method of monitoring response to islet transplantation: bioluminescent imaging of an NF-kB transgenic mouse model.

作者信息

Roth David J, Jansen E Duco, Powers Alvin C, Wang Taylor G

机构信息

Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37232, USA.

出版信息

Transplantation. 2006 Apr 27;81(8):1185-90. doi: 10.1097/01.tp.0000203808.84963.13.

DOI:10.1097/01.tp.0000203808.84963.13
PMID:16641606
Abstract

BACKGROUND

Transplantation of encapsulated pancreatic islets is a novel therapeutic approach for the treatment of Type 1 diabetes mellitus that has the potential to circumvent both a limited islet supply and immunosuppression. Current methods for scoring the biocompatibility of the alginate-based capsules that sequester Islets of Langerhans include fabrication and implantation into the peritoneal cavity of mice, incubation, retrieval via peritoneal lavage, and observation of the number of cells or cell layers surrounding the capsules. This method allows only one data point to be obtained per animal. We describe a method to measure biocompatibility real time and in situ. This method of monitoring immune response using bioluminescent technology and a nuclear factor-kappa beta (NF-kB) sensitive transgenic mouse model allows many data points to be acquired per animal, reduces the number of animals required to obtain statistically significant immune response data over time, and in turn reduces error associated with animal variability. NF-kB is a transcription factor that coordinates the inflammatory and wound healing cascades by initiating the transcription of cytokines, chemokines, adhesion molecules, and proinflammatory genes.

METHODS

Inflammation after the transplantation of five types of capsules was monitored for 6 six weeks after transplantation into the dorsal-cervical fat pad.

RESULTS

Bioluminescence over 6-week time period: Capsule group 1.0+/-.00 normalized units, Bead group 1.3+/-.26 normalized units, No coat group .96+/-.48 normalized units, Sham group .96+/-.00 normalized units, Control group .17+/-.11 normalized units.

CONCLUSIONS

This imaging modality was able to detect statistically significant differences in NF-kB activity between pre- and postoperative data points per mouse. It was also able to discern an unexpected increase in NF-kB activity due to capsule size instead of capsule wall composition over a 6-week time period.

摘要

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