Ali Aus T, Penny Clem B, Paiker Janice E, Psaras George, Ikram Faisel, Crowther Nigel J
Department of Chemical Pathology, National Health Laboratory Service, South Africa.
Ann Clin Biochem. 2006 May;43(Pt 3):207-13. doi: 10.1258/000456306776865179.
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.
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.
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.
This is the first study to show that tissue non-specific AP inhibitors can block adipogenesis in human preadipocytes.
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。
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。
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。
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。