Abstract |
Congenital hyperinsulinism (CHI) is caused by unregulated insulin release and leads to hyperinsulinaemic-hypoglycaemia (HH). Glucagon like peptide-1 (GLP-1), glucose-dependent insulinotropic peptide (GIP), peptide YY (PYY) and the enzyme; dipeptidyl peptidase-4 (DPP-4) all regulate appetite and glucose homeostasis. These proteins have been identified as possible contributors to HH but the mechanism remains poorly understood. We aimed to look at the expression pattern of pancreatic DPP-4 in children with focal and diffuse CHI (FCHI and DCHI, respectively). Using immunohistochemistry; we determined DPP-4 expression patterns in the pancreas of CHI patients. DPP-4 was found to be expressed in the pancreatic β, α and δ-cells in and around the focal area. However, it was predominantly co-localised with β-cells in the paediatric tissue samples. Additionally, proliferating β-cells expressed DPP-4 in DCHI, which was absent in the FCHI pancreas. Insulin was found to be present in the exocrine acini and duct cells of the DCHI pancreas suggestive of exocrine to endocrine transdifferentiation. Furthermore, 6 medically-unresponsive DCHI pancreatic samples showed an up-regulation of total pancreatic DPP-4 expression. In conclusion; the expression studies have shown DPP-4 to be altered in HH, however, further work is required to understand the underlying role for this enzyme.
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Authors | Sofia A Rahman, Senthil Senniappan, Maha Sherif, Sophia Tahir, Khalid Hussain |
Journal | International journal of clinical and experimental pathology
(Int J Clin Exp Pathol)
Vol. 8
Issue 7
Pg. 8199-208
( 2015)
ISSN: 1936-2625 [Electronic] United States |
PMID | 26339388
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biomarkers
- DPP4 protein, human
- Dipeptidyl Peptidase 4
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Topics |
- Adult
- Biomarkers
(analysis)
- Case-Control Studies
- Cell Proliferation
- Cell Transdifferentiation
- Congenital Hyperinsulinism
(enzymology, genetics, pathology, surgery)
- Dipeptidyl Peptidase 4
(analysis, genetics)
- Female
- Gene Expression Profiling
(methods)
- Humans
- Immunohistochemistry
- Infant
- Insulin-Secreting Cells
(enzymology)
- Male
- Oligonucleotide Array Sequence Analysis
- Pancreas
(enzymology, pathology, surgery)
- Up-Regulation
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