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Rapid in vitro formation of smooth endoplasmic reticulum aggregates within peptide‐producing islet cells
Author(s) -
Knodel Sandra,
Meda Paolo,
Orci Lelio
Publication year - 1987
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041330114
Subject(s) - endoplasmic reticulum , in vitro , islet , chemistry , microbiology and biotechnology , biochemistry , incubation , microsome , biology , biophysics , insulin , endocrinology
We report here that heptanol (3.5 mM) induces in vitro a rapid formation of smooth endoplasmic reticulum aggregates (SERA) within isolated islets of Langerhans. SERA appeared after only 15 min of exposure to the alkanol and increased in number during the first 30 min of incubation. At that time, SERA represented 2% and 6% of the volume of B‐ and non‐B‐cells, respectively. Removal of heptanol resulted in the rapid disappearance of SERA, whereas reintroduction of the alkanol rapidly induced these structures again. SERA formation was seen in different types of endocrine and nonendocrine islet cells. In the insulin‐producing B‐cells, SERA formation was not modified by conditions known to alter the secretory activity and the microtubular‐microfilament network or to inhibit protein synthesis. By contrast, SERA formation was inhibted by low temperature and by conditions depleting the energy sources of the cells. Similar observations were made in the presence of either octanol (1 mM) or nonanol (1 mM) but not of shorter chain alkanols, alkanes, oxidative derivates of either heptanol or octanol, and of other unrelated lipid soluble compounds. Incubations in the presence of long‐chain alkanols provide, therefore, a unique model to study in vitro the formation and disposal of smooth endoplasmic reticulum, as well as a system in which rapid membrane biogenesis is amenable to direct experimental testing.