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碱性磷酸酶抑制剂对从人乳腺组织分离的前脂肪细胞内脂质积累的影响。

The effect of alkaline phosphatase inhibitors on intracellular lipid accumulation in preadipocytes isolated from human mammary tissue.

作者信息

Ali Aus T, Penny Clem B, Paiker Janice E, Psaras George, Ikram Faisel, Crowther Nigel J

机构信息

Department of Chemical Pathology, National Health Laboratory Service, South Africa.

出版信息

Ann Clin Biochem. 2006 May;43(Pt 3):207-13. doi: 10.1258/000456306776865179.

Abstract

BACKGROUND

A previous study has demonstrated that alkaline phosphatase (AP) may play a role in the control of intracellular lipid accumulation in the rodent preadipocyte cell line, 3T3-L1. The present study investigated whether AP may have a similar function in preadipocytes isolated from human mammary gland tissue.

METHODS

Preadipocyte maturation was induced in the presence or absence of the tissue non-specific AP inhibitors levamisole and histidine, and the tissue-specific AP inhibitor PheGlyGly. Cellular AP activity and adipogenesis were both assessed at 0 and 12 days post-induction of differentiation.

RESULTS

After differentiation, AP activity increased 5.1 +/- 1.3-fold in the absence and 8.9 +/- 2.8-fold (P < 0.05) in the presence of levamisole. However, adipogenesis increased 1.95 +/- 0.11-fold in the absence but only 1.36 +/- 0.06-fold (P < 0.001) in the presence of levamisole. There was a 4.2 +/- 2.2-fold increase in AP activity in the absence and a 0.51 +/- 0.46-fold (P < 0.05) decrease in the presence of histidine. Adipogenesis increased 2.09 +/- 0.35-fold in the absence of histidine but only 1.22 +/- 0.30-fold (P < 0.05) in the presence of histidine. PheGlyGly had no effects. Fluorescent microscopy showed AP activity was localized to the triglyceride-containing droplets of the cell.

CONCLUSION

This is the first study to show that tissue non-specific AP inhibitors can block adipogenesis in human preadipocytes.

摘要

背景

先前的一项研究表明,碱性磷酸酶(AP)可能在啮齿动物前脂肪细胞系3T3-L1的细胞内脂质积累控制中发挥作用。本研究调查了AP在从人乳腺组织分离的前脂肪细胞中是否具有类似功能。

方法

在存在或不存在组织非特异性AP抑制剂左旋咪唑和组氨酸以及组织特异性AP抑制剂苯甘氨酰甘氨酸的情况下诱导前脂肪细胞成熟,并在诱导分化后0天和12天评估细胞AP活性和成脂作用。

结果

分化后,在不存在左旋咪唑的情况下AP活性增加了5.1±1.3倍,在存在左旋咪唑的情况下增加了8.9±2.8倍(P<0.05)。然而,在不存在左旋咪唑的情况下成脂作用增加了1.95±0.11倍,而在存在左旋咪唑的情况下仅增加了1.36±0.06倍(P<0.001)。在不存在组氨酸的情况下AP活性增加了4.2±2.2倍,在存在组氨酸的情况下减少了0.51±0.46倍(P<0.05)。在不存在组氨酸的情况下成脂作用增加了2.09±0.35倍,而在存在组氨酸的情况下仅增加了1.22±0.30倍(P<0.05)。苯甘氨酰甘氨酸没有作用。荧光显微镜检查显示AP活性定位于细胞中含甘油三酯的脂滴。

结论

这是第一项表明组织非特异性AP抑制剂可阻断人前脂肪细胞成脂作用的研究。

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