Abstract
Messenger RNA from intact rat pancreatic islets, or from transformed hamster beta (HIT) cells, hybridized with the cDNA probe for type I (but not type II) phospholipase A2. The levels of phospholipase A2 mRNA increased in islets from fasted rats: they decreased in islets cultured in a high glucose concentration (control values at 5.5 mM glucose = 150±6% of those at 22 mM) which impaired subsequent insulin secretion (reduction in second-phase release = 70±11%). These studies uniquely demonstrate that type I phospholipase A2 is expressed specifically in beta cells and that nutrient availability modulates transcript levels, an effect which could contribute to the detrimental influence of prolonged hyperglycemia on islet function.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 110-112 |
| Number of pages | 3 |
| Journal | FEBS Letters |
| Volume | 295 |
| Issue number | 1-3 |
| DOIs | |
| State | Published - Dec 16 1991 |
Keywords
- Beta cell
- Fasting
- Glucose
- Insulin
- Pancreatic islet
- Phospholipase