| First Author | Kruit JK | Year | 2011 |
| Journal | Diabetes | Volume | 60 |
| Issue | 12 | Pages | 3186-96 |
| PubMed ID | 21998401 | Mgi Jnum | J:189451 |
| Mgi Id | MGI:5445830 | Doi | 10.2337/db11-0081 |
| Citation | Kruit JK, et al. (2011) Islet cholesterol accumulation due to loss of ABCA1 leads to impaired exocytosis of insulin granules. Diabetes 60(12):3186-96 |
| abstractText | OBJECTIVE: The ATP-binding cassette transporter A1 (ABCA1) is essential for normal insulin secretion from beta-cells. The aim of this study was to elucidate the mechanisms underlying the impaired insulin secretion in islets lacking beta-cell ABCA1. RESEARCH DESIGN AND METHODS: Calcium imaging, patch clamp, and membrane capacitance were used to assess the effect of ABCA1 deficiency on calcium flux, ion channel function, and exocytosis in islet cells. Electron microscopy was used to analyze beta-cell ultrastructure. The quantity and distribution of proteins involved in insulin-granule exocytosis were also investigated. RESULTS: We show that a lack of beta-cell ABCA1 results in impaired depolarization-induced exocytotic fusion of insulin granules. We observed disturbances in membrane microdomain organization and Golgi and insulin granule morphology in beta-cells as well as elevated fasting plasma proinsulin levels in mice in the absence of beta-cell ABCA1. Acute cholesterol depletion rescued the exocytotic defect in beta-cells lacking ABCA1, indicating that elevated islet cholesterol accumulation directly impairs granule fusion and insulin secretion. CONCLUSIONS: Our data highlight a crucial role of ABCA1 and cellular cholesterol in beta-cells that is necessary for regulated insulin granule fusion events. These data suggest that abnormalities of cholesterol metabolism may contribute to the impaired beta-cell function in diabetes. |
