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Zn2+-transporter-8: A dual role in diabetes
- Source :
- BioFactors. 35:356-363
- Publication Year :
- 2009
- Publisher :
- Wiley, 2009.
-
Abstract
- Diabetes mellitus arises from defects in insulin secretion or action, or both. In pancreatic islets, insulin production is linked with zinc transport mediated by zinc transporter ZnT-8, a product of the SLC30A8 gene. Therefore, altered activity of ZnT-8 is expected to be associated with impaired glucose-induced insulin response and promote progression from glucose intolerance to diabetes. Recent findings do emerge with a role of SLC30A8 in diabetes. Genome-wide association scans for type 2 diabetes (T2D) susceptibility loci revealed and then replicated a highly significant association between the R allele of the R325W variant of SLC30A8 (marker rs13266634) and susceptibility to T2D in Caucasians. A role of ZnT-8 as a new major self-antigenic determinant in type 1 diabetes (T1D) was found. Marker rs13266634 was also shown to modulate anti-ZnT-8 self-antibody specificity in islet autoimmunity. Hence, these findings suggest for a dual role of SLC30A8 in diabetes, which is consisted in conferring genetic susceptibility to T2D and being a major islet self-antigen in T1D as well. Here we characterize an emerging role of ZnT-8 in diabetes and discuss potential mechanisms of its involvement in the etiology of both forms of diabetes.
- Subjects :
- medicine.medical_specialty
endocrine system diseases
medicine.medical_treatment
Clinical Biochemistry
Zinc Transporter 8
Type 2 diabetes
Biochemistry
Diabetes mellitus genetics
Internal medicine
Diabetes mellitus
Insulin Secretion
Diabetes Mellitus
medicine
Humans
Insulin
Cation Transport Proteins
Type 1 diabetes
SLC30A8
biology
General Medicine
medicine.disease
Zinc
Diabetes Mellitus, Type 1
Endocrinology
Diabetes Mellitus, Type 2
biology.protein
Molecular Medicine
TCF7L2
Subjects
Details
- ISSN :
- 18728081 and 09516433
- Volume :
- 35
- Database :
- OpenAIRE
- Journal :
- BioFactors
- Accession number :
- edsair.doi.dedup.....1b37438a8a4af93e1ea6a61db611b343
- Full Text :
- https://doi.org/10.1002/biof.49