Hormone-sensitive lipase expression and activity in relation to lipolysis in human fat cells

Autor: Jacques Grober, Vanessa van Harmelen, Peter Arner, Dominique Langin, Signy Reynisdottir, Cecilia Holm, Valérie Large
Přispěvatelé: Institut Louis Bugnard, Large, Valerie
Jazyk: angličtina
Rok vydání: 1998
Předmět:
Male
Hormone-sensitive lipase
White adipose tissue
Biochemistry
MESH: Isoproterenol
Adenylyl cyclase
chemistry.chemical_compound
0302 clinical medicine
Endocrinology
Adipocyte
Adipocytes
MESH: Obesity
MESH: Genetic Variation
MESH: Cell Size
0303 health sciences
Forskolin
MESH: Sterol Esterase
biology
MESH: Kinetics
Immunochemistry
MESH: Molecular Weight
food and beverages
Female
catecholamines
Adult
medicine.medical_specialty
Lipolysis
030209 endocrinology & metabolism
QD415-436
In Vitro Techniques
03 medical and health sciences
white adipose tissue
Internal medicine
medicine
Humans
MESH: Lipolysis
Obesity
RNA
Messenger

Lipase
MESH: Adipocytes
030304 developmental biology
Cell Size
MESH: RNA
Messenger

MESH: In Vitro Techniques
MESH: Humans
Activator (genetics)
MESH: Immunochemistry
Isoproterenol
Genetic Variation
MESH: Adult
Cell Biology
Sterol Esterase
β-adrenoceptors
MESH: Male
Molecular Weight
[SDV.AEN] Life Sciences [q-bio]/Food and Nutrition
Kinetics
chemistry
lipid mobilization
biology.protein
MESH: Female
[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
Zdroj: Journal of Lipid Research
Journal of Lipid Research, American Society for Biochemistry and Molecular Biology, 1998, 39 (8), pp.1688-95
Journal of Lipid Research, Vol 39, Iss 8, Pp 1688-1695 (1998)
Karolinska Institutet
Europe PubMed Central
ISSN: 0022-2275
Popis: Hormone-sensitive lipase (HSL) catalyzes the rate-limiting step in adipocyte lipolysis. The activity of HSL is thought to be primarily regulated by reversible phosphorylation. However, the regulation of HSL activity by pretranslational mechanisms has been poorly studied. The present studies were undertaken to explore the relationship between the levels of HSL protein and mRNA expressions and the lipolytic capacity. The study was performed in human abdominal subcutaneous adipocytes with identical sizes but having either a high (HL) or low (LL) lipolytic capacity (n = 16). Basal and maximal lipolysis induced by catecholamines, an adenylyl cyclase activator forskolin, and a cyclic AMP analogue dibutyryl cAMP were 50% lower in LL- in comparison with HL-fat cells (P < 0.05 or better). No differences in drug sensitivity were found. HSL activity and quantity were about 50% lower in LL- compared with HL-fat cells (P < 0.05). Moreover, the mRNA ratio between HSL and γ-actin was 35% lower in LL-compared with HL-fat cells (P < 0.05). There was a strong linear correlation between the protein and enzymatic HSL measurements (r2 = 0.91). In addition, the maximum lipolytic capacity was significantly correlated with HSL activity (r 2 = 0.75) and HSL protein amount (r 2 = 0.64). It is concluded that hormone-sensitive lipase (HSL) expression, measured either as total HSL protein by Western blot analysis or as total amount of activatable HSL enzyme, is a major determinant of the maximum lipolytic capacity of human fat cells. In addition, HSL protein expression is at least, in part, determined by HSL mRNA expression.—Large, V., P. Arner, S. Reynisdottir, J. Grober, V. Van Harmelen, C. Holm, and D. Langin. Hormone-sensitive lipase expression and activity in relation to lipolysis in human fat cells.
Databáze: OpenAIRE