bioRxiv · 10.1101/2022.06.28.498031
Hypoxia causes pancreatic β-cell dysfunction by activating a transcriptional repressor BHLHE40
Abstract
Hypoxia can occur in pancreatic {beta}-cells in type 2 diabetes. Although hypoxia exerts deleterious effects on {beta}-cell function, the associated mechanisms are largely unknown. Here, we show that the transcriptional repressor basic helix-loop-helix family member e40 (BHLHE40) is highly induced in hypoxic mouse and human {beta}-cells and suppresses insulin secretion. Conversely, BHLHE40 deficiency in hypoxic MIN6 cells or in the {beta}-cells of ob/ob mice reversed the insulin secretion. Mechanistically, BHLHE40 represses expression of Mafa, which encodes the transcription factor musculoaponeurotic fibrosarcoma oncogene family A (MAFA), by attenuating binding of pancreas/duodenum homeobox protein 1 (PDX1) to its enhancer region. Impaired insulin secretion in hypoxic {beta}-cells was recovered by MAFA expression. Collectively, this work identifies BHLHE40 as a key hypoxia-induced transcriptional repressor in {beta}-cells and its implication in the {beta}-cell dysfunction in type 2 diabetes.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Tsuyama, T., Sato, Y., Yoshizawa, T., Matsuoka, T., Yamagata, K.. 2022-06-29. Hypoxia causes pancreatic β-cell dysfunction by activating a transcriptional repressor BHLHE40. https://doi.org/10.1101/2022.06.28.498031
Cite the original work for its findings. Save a collection to share your selection of sources.