A new immunodeficient hyperglycaemic mouse model based on the Ins2Akita mutation for analyses of human islet and beta stem and progenitor cell function
Authors
Pearson, ToddShultz, Leonard D.
Lief, J.
Burzenski, Lisa M.
Gott, Bruce
Chase, T.
Foreman, Oded
Rossini, Aldo A.
Bottino, Rita
Trucco, Massimo
Greiner, Dale L.
UMass Chan Affiliations
Department of Medicine, Division of DiabetesDocument Type
Journal ArticlePublication Date
2008-06-20Keywords
AnimalsCord Blood Stem Cell Transplantation
Disease Models, Animal
Humans
Hyperglycemia
Insulin-Secreting Cells
Islets of Langerhans
*Islets of Langerhans Transplantation
Mice
Mice, Inbred NOD
*Mutation
Receptors, Interleukin-2
Severe Combined Immunodeficiency
Transplantation, Heterologous
Life Sciences
Medicine and Health Sciences
Metadata
Show full item recordAbstract
AIMS/HYPOTHESIS: To develop and validate a new immunodeficient mouse strain that spontaneously develops a non-autoimmune hyperglycaemia to serve as a diabetic host for human islets and human beta stem and progenitor cells without the need for induction of hyperglycaemia by toxic chemicals with their associated side effects. METHODS: We generated and characterised a new strain of immunodeficient spontaneously hyperglycaemic mice, the NOD-Rag1null Prf1null Ins2Akita strain and compared this strain with the NOD-scid Il2rgammanull (also known as Il2rg) immunodeficient strain rendered hyperglycaemic by administration of a single dose of streptozotocin. Hyperglycaemic mice were transplanted with human islets ranging from 1,000 to 4,000 islet equivalents (IEQ) and were monitored for normalisation of blood glucose levels. RESULTS: NOD-Rag1null Prf1null Ins2Akita mice developed spontaneous hyperglycaemia, similar to Ins2Akita-harbouring strains of immunocompetent mice. Histological examination of islets in the host pancreas validated the spontaneous loss of beta cell mass in the absence of mononuclear cell infiltration. Human islets transplanted into spontaneously diabetic NOD-Rag1null Prf1null Ins2Akita and chemically diabetic NOD-scid Il2rgammanull mice resulted in a return to euglycaemia that occurred with transplantation of similar beta cell masses. CONCLUSIONS/INTERPRETATION: The NOD-Rag1null Prf1null Ins2Akita mouse is the first immunodeficient, spontaneously hyperglycaemic mouse strain described that is based on the Ins2Akita mutation. This strain is suitable as hosts for human islet and human beta stem and progenitor cell transplantation in the absence of the need for pharmacological induction of diabetes. This strain of mice also has low levels of innate immunity and can be engrafted with a human immune system for the study of human islet allograft rejection.Source
Diabetologia. 2008 Aug;51(8):1449-56. Epub 2008 Jun 19. Link to article on publisher's site
DOI
10.1007/s00125-008-1057-1Permanent Link to this Item
http://hdl.handle.net/20.500.14038/39202PubMed ID
18563383Related Resources
ae974a485f413a2113503eed53cd6c53
10.1007/s00125-008-1057-1