Abstract
Neurogenin 3 (NGN3) commits pancreatic progenitors to an islet cell fate. We have induced NGN3 expression and identified upregulation of the gene encoding the Ras-associated small molecular mass GTP-binding protein, RAB3B. RAB3B localised to the cytoplasm of human β-cells, both during the foetal period and post natally. Genes encoding alternative RAB3 proteins and RAB27A were unaltered by NGN3 expression and in human adult islets their transcripts were many fold less prevalent than those of RAB3B. The regulation of insulin exocytosis in rodent β-cells and responsiveness to incretins are reliant on Rab family members, notably Rab3a and Rab27a, but not Rab3b. Our results support an important inter-species difference in regulating insulin exocytosis where RAB3B is the most expressed isoform in human islets.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Basic Helix-Loop-Helix Transcription Factors / genetics
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Basic Helix-Loop-Helix Transcription Factors / metabolism*
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Cells, Cultured
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Fetus
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Gene Expression Regulation / physiology*
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Glucagon / metabolism
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Humans
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Insulin / metabolism
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Islets of Langerhans / metabolism*
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Nerve Tissue Proteins / genetics
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Nerve Tissue Proteins / metabolism*
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Protein Isoforms
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RNA / genetics
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RNA / metabolism
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rab GTP-Binding Proteins / genetics
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rab GTP-Binding Proteins / metabolism
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rab27 GTP-Binding Proteins
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rab3 GTP-Binding Proteins / genetics
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rab3 GTP-Binding Proteins / metabolism*
Substances
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Basic Helix-Loop-Helix Transcription Factors
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Insulin
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NEUROG3 protein, human
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Nerve Tissue Proteins
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Protein Isoforms
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rab27 GTP-Binding Proteins
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RNA
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Glucagon
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RAB3B protein, human
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RAB27A protein, human
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rab GTP-Binding Proteins
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rab3 GTP-Binding Proteins