Artikel ; Online: A Novel Intron-Encoded Neuropilin-1 Isoform in Pancreatic Islets Associated With Very Young Age of Onset of Type 1 Diabetes.
2022 Band 71, Heft 9, Seite(n) 2058–2063
Abstract: Net synthesis of pancreatic β-cells peaks before 2 years of life. β-Cell mass is set within the first 5 years of life. In-frame translational readthrough of the NRP1 gene exon 9 into intron 9 generates a truncated neuropilin-1 protein lacking downstream ... ...
Abstract | Net synthesis of pancreatic β-cells peaks before 2 years of life. β-Cell mass is set within the first 5 years of life. In-frame translational readthrough of the NRP1 gene exon 9 into intron 9 generates a truncated neuropilin-1 protein lacking downstream sequence necessary for binding VEGF that stimulates β-cell replication. VEGF is critical for developing but not adult islet neogenesis. Herein we show that cells in human pancreatic islets containing the full-length neuropilin-1 possess insulin but cells that contain the truncated neuropilin-1 are devoid of insulin. Decreased insulin cells increases susceptibility to onset of type 1 diabetes at a younger age. We also show that the frequency of a genetic marker in NRP1 intron 9 is higher among patients with onset of type 1 diabetes before age 4 years (31.8%), including those with onset at 0.67-2.00 and 2-4 years, compared with that in patients with onset at 4-8 years, at 8-12 years, and after 16 years (16.1%) with frequency equal to that in subjects without diabetes (16.0%). Decreased insulin cells plus the genetic data are consistent with a low effect mechanism that alters the onset of type 1 diabetes to a very young age in some patients, thus supporting the endotype concept that type 1 diabetes is a heterogeneous disease. |
|||||
---|---|---|---|---|---|---|
Mesh-Begriff(e) | Age of Onset ; Child, Preschool ; Diabetes Mellitus, Type 1/genetics ; Diabetes Mellitus, Type 1/metabolism ; Humans ; Insulin/metabolism ; Introns/genetics ; Islets of Langerhans/metabolism ; Neuropilin-1/genetics ; Neuropilin-1/metabolism ; Protein Isoforms/genetics ; Vascular Endothelial Growth Factor A/metabolism | |||||
Chemische Substanzen | Insulin ; Protein Isoforms ; Vascular Endothelial Growth Factor A ; Neuropilin-1 (144713-63-3) | |||||
Sprache | Englisch | |||||
Erscheinungsdatum | 2022-06-17 | |||||
Erscheinungsland | United States | |||||
Dokumenttyp | Journal Article ; Research Support, Non-U.S. Gov't | |||||
ZDB-ID | 80085-5 | |||||
ISSN | 1939-327X ; 0012-1797 | |||||
ISSN (online) | 1939-327X | |||||
ISSN | 0012-1797 | |||||
DOI | 10.2337/db21-1070 | |||||
Signatur |
|
|||||
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
Zusatzmaterialien
Kategorien
Verfügbar in ZB MED Köln/Königswinter
Uh III Zs.175: Hefte anzeigen | Standort: Je nach Verfügbarkeit (siehe Angabe bei Bestand) bis Jg. 2021: Bestellungen von Artikeln über das Online-Bestellformular ab Jg. 2022: Lesesaal (EG) |
Über subito bestellen
Dieser Service ist kostenpflichtig (siehe Lieferbedingungen von subito). Bestellungen, die einen Artikel nebst Supplementary Material umfassen, werden grundsätzlich wie mehrfache Bestellungen bearbeitet. Gebühren fallen in diesen Fällen für jede einzelne Bestellung an.