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Updated: Aug 20, 2025

Isolation and Decellularization of a Whole Porcine Pancreas
Published on: October 10, 2018
Tissue engineering of decellularized pancreas scaffolds for regenerative medicine in diabetes
Lillian Yuxian Lim1, Shirley Suet Lee Ding1, Padmalosini Muthukumaran2
1Stem Cells and Diabetes Laboratory, Institute of Molecular and Cell Biology (IMCB), A*STAR, Singapore.
Abstract:
Diabetes mellitus is a global disease requiring long-term treatment and monitoring. At present, pancreas or islet transplantation is the only reliable treatment for achieving stable euglycemia in Type I diabetes patients. However, the shortage of viable pancreata for transplantation limits the use of this therapy for the majority of patients. Organ decellularization and recellularization is emerging as a promising solution to overcome the shortage of viable organs for transplantation by providing a potential alternative source of donor organs. Several studies on decellularization and recellularization of rodent, porcine, and human pancreata have been performed, and show promise for generating usable decellularized pancreas scaffolds for subsequent recellularization and transplantation. In this state-of-the-art review, we provide an overview of the latest advances in pancreas decellularization, recellularization, and revascularization. We also discuss clinical considerations such as potential transplantation sites, donor source, and immune considerations. We conclude with an outlook on the remaining work that needs to be done in order to realize the goal of using this technology to create bioengineered pancreata for transplantation in diabetes patients. STATEMENT OF SIGNIFICANCE: Pancreas or islet transplantation is a means of providing insulin-independence in diabetes patients. However, due to the shortage of viable pancreata, whole-organ decellularization and recellularization is emerging as a promising solution to overcome organ shortage for transplantation. Several studies on decellularization and recellularization of rodent, porcine, and human pancreata have shown promise for generating usable decellularized pancreas scaffolds for subsequent recellularization and transplantation. In this state-of-the-art review, we highlight the latest advances in pancreas decellularization, recellularization, and revascularization. We also discuss clinical considerations such as potential transplantation sites, donor source, and immune considerations. We conclude with future work that needs to be done in order to realize clinical translation of bioengineered pancreata for transplantation in diabetes patients.
Insights
Organ decellularization and recellularization offers a promising solution to the shortage of donor pancreata for diabetes patients. This review covers advances in bioengineering pancreas scaffolds for transplantation.
Area of Science:
- Regenerative Medicine
- Transplantation Biology
- Biomaterials Engineering
Background:
- Diabetes mellitus is a global health challenge requiring lifelong management.
- Pancreas or islet transplantation is the only definitive treatment for stable euglycemia in Type I diabetes.
- Donor organ shortage severely limits transplantation accessibility.
Purpose of the Study:
- To review the latest advancements in pancreas decellularization and recellularization techniques.
- To discuss the potential of bioengineered pancreata for transplantation.
- To explore clinical considerations for future pancreas bioengineering.
Main Methods:
- Review of current literature on organ decellularization and recellularization.
- Analysis of studies involving decellularization of rodent, porcine, and human pancreata.
- Discussion of revascularization strategies and clinical transplantation factors.
Main Results:
- Decellularization and recellularization show promise for creating functional pancreas scaffolds.
- Successful decellularization and recellularization have been demonstrated across various species.
- Key challenges include achieving adequate revascularization and addressing immune responses.
Conclusions:
- Bioengineered pancreata hold significant potential to overcome donor organ scarcity.
- Further research is needed to optimize scaffold fabrication, cell seeding, and vascularization.
- Clinical translation requires addressing donor source, transplantation sites, and immunological challenges.

