首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >The relationship between alkaline phosphatase activity and intracellular lipid accumulation in murine 3T3-L1 cells and human preadipocytes
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The relationship between alkaline phosphatase activity and intracellular lipid accumulation in murine 3T3-L1 cells and human preadipocytes

机译:鼠3T3-L1细胞和人脂肪细胞中碱性磷酸酶活性与细胞内脂质蓄积的关系

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Alkaline phosphatase (ALP) is expressed in 3T3-L1 preadipocytes, and its activity increases during adipogenesis. The purpose of this study was to determine whether ALP activity Could be used as a measure of intracellular lipid accumulation in human preadipocytes and 3T3-L1 cells and which of the factors that induce adipogenesis are responsible for stimulating ALP activity. Adipogenesis was initiated in 3T3-L1 cells by incubation with differentiation medium containing insulin. dexamethasone. and 3-isobutyl-1methylxanthine. The effect of leaving out each of the differentiation medium components was, studied. Adipogenesis was also assessed in human preadipocytes and 3T3-L1 cells in the presence of the ALP inhibitor histidine. ALP activity was measured Using an automated colorimetric assay and intracellular lipid accumulation was measured using the lipid-specific dye oil red O. Removal of insulin or dexamethasone from the differentiation medium had little effect on either ALP activity or lipid accumulation in 3T3-L1 cells, while removal of IBMX blocked both. Histidine inhibited ALP activity and adipogenesis in human preadipocytes and 3T3-L1 cells. Pearson univariate correlation analysis demonstrated strong correlations between ALP activity and lipid accumulation in human preadipocytes (r = 0.78, n = 69) and in 3T3-L1 cells (r = 0.92, it = 27). These data suggest that ALP and fat storage are tightly linked during preadipocyte maturation and that the measurement of ALP activity my be a novel technique for the quantification of intracellular lipid accumulation that is more sensitive and rapid than currently used methods. (c) 2006 Elsevier Inc. All rights reserved.
机译:碱性磷酸酶(ALP)在3T3-L1前脂肪细胞中表达,其活性在脂肪形成过程中增加。这项研究的目的是确定是否可以将ALP活性用作人类前脂肪细胞和3T3-L1细胞中细胞内脂质蓄积的量度,以及哪些诱导脂肪形成的因素可刺激ALP活性。通过与含胰岛素的分化培养基孵育,在3T3-L1细胞中开始脂肪形成。地塞米松。和3-异丁基-1甲基黄嘌呤。研究了省略每种分化培养基成分的效果。在存在ALP抑制剂组氨酸的情况下,还评估了人类前脂肪细胞和3T3-L1细胞中的脂肪形成。使用自动比色法测量ALP活性,并使用脂质特异性染料油红O测量细胞内脂质蓄积。从分化培养基中去除胰岛素或地塞米松对3T3-L1细胞中的ALP活性或脂质蓄积几乎没有影响,而删除IBMX则同时阻止了这两个过程。组氨酸抑制人前脂肪细胞和3T3-L1细胞中的ALP活性和脂肪形成。皮尔森单变量相关分析表明,人类前脂肪细胞(r = 0.78,n = 69)和3T3-L1细胞(r = 0.92,n = 27)中ALP活性与脂质蓄积之间存在很强的相关性。这些数据表明,在脂肪前细胞成熟过程中,ALP和脂肪储存紧密相连,并且ALP活性的测定是一种比目前使用的方法更灵敏,更快速的定量细胞内脂质蓄积的新技术。 (c)2006 Elsevier Inc.保留所有权利。

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