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Generation of Transplantable Beta Cells for Patient-Specific Cell Therapy
Author(s) -
Xiaojie Wang,
Daniel L. Metzger,
Mark Meloche,
Jianqiang Hao,
Ziliang Ao,
Garth L. Warnock
Publication year - 2012
Publication title -
international journal of endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.875
H-Index - 60
eISSN - 1687-8345
pISSN - 1687-8337
DOI - 10.1155/2012/414812
Subject(s) - medicine , beta cell , beta (programming language) , immunosuppression , somatic cell , heterologous , cell therapy , transplantation , cell , islet , regeneration (biology) , cancer research , insulin , immunology , microbiology and biotechnology , biology , biochemistry , computer science , gene , programming language
Islet cell transplantation offers a potential cure for type 1 diabetes, but it is challenged by insufficient donor tissue and side effects of current immunosuppressive drugs. Therefore, alternative sources of insulin-producing cells and isletfriendly immunosuppression are required to increase the efficiency and safety of this procedure. Beta cells can be transdifferentiated from precursors or another heterologous (non-beta-cell) source. Recent advances in beta cell regeneration from somatic cells such as fibroblasts could circumvent the usage of immunosuppressive drugs. Therefore, generation of patient-specific beta cells provides the potential of an evolutionary treatment for patients with diabetes.

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