Department of Medicine Huddinge and Endocrine-Metabolic Clinic, Karolinska Institutet, Karolinska University Hospital Huddinge, M63, SE-141 86 Stockholm, Sweden.
J Clin Endocrinol Metab. 2011 Dec;96(12):E2045-9. doi: 10.1210/jc.2011-1702. Epub 2011 Oct 12.
Large fat cell size is linked to type 2 diabetes risk and may involve an enhanced rate of adipocyte lipolysis causing elevated levels of fatty acids.
Our objective was to study the role of fat cell size in the regulation of lipolysis within a subject.
Subcutaneous adipose tissue was obtained from 16 healthy subjects. Large and small adipocytes were isolated for each sample. Hormonal regulation of lipolysis and expression of lipolysis-regulating proteins were investigated.
No effect of cell size on the rate of lipolysis was observed when lipolysis was expressed per lipid weight of fat cells. However, when expressed per number of fat cells, the lipolysis was significantly higher in large as compared with small adipocytes. This was observed in both the unstimulated (basal) state and in the presence of the major lipolysis-regulating hormones such as catecholamines (stimulating), natriuretic peptides (stimulating), and insulin (inhibiting). The receptor properties (number, affinity, and coupling) for these hormones did not differ between large and small adipocytes. However, the expression of proteins regulating the final steps in hormone signaling to lipolysis (hormone-sensitive lipase, adipose triglyceride lipase, and perilipin) was increased in large adipocytes.
Independently of the donor, sc fat cell size per se determines lipolysis rates. Large adipocytes have increased lipolytic capacity, probably due to the enrichment of regulatory proteins distal in the lipolytic cascade, to which all lipolytic signals converge (lipases and perilipin). Enhanced lipolytic capacity may link adipocyte hypertrophy to the risk of developing type 2 diabetes.
大脂肪细胞大小与 2 型糖尿病风险相关,可能涉及脂肪细胞脂解率增强,导致脂肪酸水平升高。
我们的目的是研究脂肪细胞大小在个体脂解调节中的作用。
从 16 名健康受试者中获得皮下脂肪组织。为每个样本分离大、小脂肪细胞。研究了脂解的激素调节和脂解调节蛋白的表达。
当以脂肪细胞的脂质重量表示时,细胞大小对脂解率没有影响。然而,当以脂肪细胞数量表示时,大脂肪细胞的脂解率明显高于小脂肪细胞。这种情况在未刺激(基础)状态和主要脂解调节激素(如儿茶酚胺(刺激)、利钠肽(刺激)和胰岛素(抑制))存在的情况下都观察到。这些激素的受体特性(数量、亲和力和偶联)在大、小脂肪细胞之间没有差异。然而,调节激素信号到脂解的最终步骤的蛋白(激素敏感脂肪酶、脂肪甘油三酯脂肪酶和脂联素)的表达在大脂肪细胞中增加。
独立于供体,sc 脂肪细胞大小本身决定了脂解率。大脂肪细胞具有增强的脂解能力,可能是由于在脂解级联的下游富含调节蛋白,所有脂解信号都汇聚于此(脂肪酶和脂联素)。增强的脂解能力可能将脂肪细胞肥大与 2 型糖尿病的发病风险联系起来。