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Nutritional, hormonal, and depot-dependent regulation of the expression of the small GTPase Rab18 in rodent adipose tissue.

Authors :
Pulido MR
Rabanal-Ruiz Y
Almabouada F
Díaz-Ruiz A
Burrell MA
Vázquez MJ
Castaño JP
Kineman RD
Luque RM
Diéguez C
Vázquez-Martínez R
Malagón MM
Source :
Journal of molecular endocrinology [J Mol Endocrinol] 2012 Dec 31; Vol. 50 (1), pp. 19-29. Date of Electronic Publication: 2012 Dec 31 (Print Publication: 2013).
Publication Year :
2012

Abstract

There is increasing evidence that proteins associated with lipid droplets (LDs) play a key role in the coordination of lipid storage and mobilization in adipocytes. The small GTPase, RAB18, has been recently identified as a novel component of the protein coat of LDs and proposed to play a role in both β-adrenergic stimulation of lipolysis and insulin-induced lipogenesis in 3T3-L1 adipocytes. In order to better understand the role of Rab18 in the regulation of lipid metabolism in adipocytes, we evaluated the effects of age, fat location, metabolic status, and hormonal milieu on Rab18 expression in rodent white adipose tissue (WAT). Rab18 mRNA was undetectable at postnatal day 15 (P15), but reached adult levels by P45, in both male and female rats. In adult rats, Rab18 immunolocalized around LDs, as well as within the cytoplasm of mature adipocytes. A weak Rab18 signal was also detected in the stromal-vascular fraction of WAT. In mice, fasting significantly increased, though with a distinct time-course pattern, Rab18 mRNA and protein levels in visceral and subcutaneous WAT. The expression of Rab18 was also increased in visceral and subcutaneous WAT of obese mice (diet-induced, ob/ob, and New Zealand obese mice) compared with lean controls. Rab18 expression in rats was unaltered by castration, adrenalectomy, or GH deficiency but was increased by hypophysectomy, as well as hypothyroidism. When viewed together, our results suggest the participation of Rab18 in the regulation of lipid processing in adipose tissue under both normal and pathological conditions.

Details

Language :
English
ISSN :
1479-6813
Volume :
50
Issue :
1
Database :
MEDLINE
Journal :
Journal of molecular endocrinology
Publication Type :
Academic Journal
Accession number :
23093555
Full Text :
https://doi.org/10.1530/JME-12-0140