Abstract
We investigated the effects of temperature on white adipocyte exocytosis (measured as increase in membrane capacitance) and short-term adiponectin secretion with the aim to elucidate mechanisms important in regulation of white adipocyte stimulus-secretion coupling. Exocytosis stimulated by cAMP (included in the pipette solution together with 3 mM ATP) in the absence of Ca2+ (10 mM intracellular EGTA) was equal at all investigated temperatures (23°C, 27°C, 32°C and 37°C). However, the augmentation of exocytosis induced by an elevation of the free cytosolic [Ca2+] to ~1.5 μM (9 mM Ca2+ + 10 mM EGTA) was potent at 32°C or 37°C but less distinct at 27°C and abolished at 23°C. Adiponectin secretion stimulated by 30 min incubations with the membrane permeable cAMP analogue 8-Br-cAMP (1 mM) or a combination of 10 μM forskolin and 200 μM IBMX was unaffected by a reduction of temperature from 32°C to 23°C. At 32°C, cAMP-stimulated secretion was 2-fold amplified by inclusion of the Ca2+ ionophore ionomycin (1μM), an effect that was not observed at 23°C. We suggest that cooling affects adipocyte exocytosis/adiponectin secretion at a Ca2+-dependent step, likely involving ATP-dependent processes, important for augmentation of cAMP-stimulated adiponectin release.
Highlights
White adipose tissue is an endocrine organ that secretes a variety of hormone-like protein factors, commonly referred to as adipokines
Our study shows that exocytosis/adiponectin secretion in white adipocytes, in addition to temperature-independent processes, comprises temperaturedependent components involving Ca2+
We have recently shown that an elevation of cytosolic Ca2+ is necessary in order to achieve robust cAMP-stimulated adiponectin secretion as well as to maintain secretion over longer time-periods
Summary
White adipose tissue is an endocrine organ that secretes a variety of hormone-like protein factors, commonly referred to as adipokines. Adiponectin is a protein hormone secreted exclusively from white adipose cells and involved in modulation of glucose and lipid metabolism [1]. Regulated exocytosis has been investigated in several neuroendocrine cell types and is known to involve Ca2+, ATP and temperature-dependent steps [2]. Adiponectin has been suggested to be secreted via regulated exocytosis of a pre-stored pool of secretory vesicles [3,4] but very little is known about stimulus-secretion coupling in the white adipocyte. Our recent work has shown that adipocyte exocytosis/adiponectin secretion is stimulated via PKA-independent cAMP-stimulation in a Ca2+-independent manner and is amply augmented by a combination.
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have