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9顺式、11反式和10反式、12顺式共轭亚油酸对人CD14 +单核细胞破骨细胞形成及活性的影响。

Effects of 9cis,11trans and 10trans,12cis CLA on osteoclast formation and activity from human CD14+ monocytes.

作者信息

Platt Ilana, El-Sohemy Ahmed

机构信息

Department of Nutritional Sciences, University of Toronto, Ontario, Canada.

出版信息

Lipids Health Dis. 2009 Apr 29;8:15. doi: 10.1186/1476-511X-8-15.

Abstract

BACKGROUND

Mixed CLA isomers variably affect bone resorption in animals and decrease osteoclast formation and activity in murine osteoclasts. These variable effects may be due to the different isomers present in commercial preparations of CLA, and the effects of the predominant individual isomers, 9cis,11trans (9,11) and 10trans,12cis (10,12) CLA are not clear. The objectives of this study were to determine the effects of the individual CLA isomers on osteoclast formation and activity from human CD14+ monocytes, and to determine whether any changes are accompanied by changes in cathepsin K, matrix metalloproteinase-9 (MMP-9), receptor activator of NF-kappaB (RANK) and tumour necrosis factor alpha (TNFalpha) gene expression. Osteoclasts were identified as TRAP+ multinucleated cells. Osteoclast activity was quantified by the amount of TRAP in the cultured media.

RESULTS

At 50 microM, 9,11 CLA inhibited osteoclast formation by approximately 70%, and both 9,11 and 10,12 CLA decreased osteoclast activity by approximately 85-90%. Both isomers inhibited cathepsin K (50 microM 9,11 by approximately 60%; 10,12 by approximately 50%) and RANK (50 microM 9,11 by approximately 85%; 50 microM 10,12 by approximately 65%) expression, but had no effect on MMP-9 or TNFalpha expression.

CONCLUSION

9,11 CLA inhibits osteoclast formation and activity from human cells, suggesting that this isomer may prevent bone resorption in humans. Although 10,12 CLA did not significantly reduce osteoclast formation, it reduced osteoclast activity and cathepsin K and RANK expression, suggesting that this isomer may also affect bone resorption.

摘要

背景

混合共轭亚油酸(CLA)异构体对动物的骨吸收有不同影响,并可减少小鼠破骨细胞的形成和活性。这些不同的影响可能归因于CLA商业制剂中存在的不同异构体,而主要的单一异构体9顺式,11反式(9,11)和10反式,12顺式(10,12)CLA的影响尚不清楚。本研究的目的是确定单一CLA异构体对人CD14 +单核细胞破骨细胞形成和活性的影响,并确定是否有任何变化伴随着组织蛋白酶K、基质金属蛋白酶-9(MMP-9)、核因子κB受体活化剂(RANK)和肿瘤坏死因子α(TNFα)基因表达的变化。破骨细胞被鉴定为抗酒石酸酸性磷酸酶(TRAP)阳性多核细胞。通过培养基中TRAP的量来定量破骨细胞活性。

结果

在50微摩尔浓度时,9,11 CLA抑制破骨细胞形成约70%,9,11和10,12 CLA均使破骨细胞活性降低约85 - 90%。两种异构体均抑制组织蛋白酶K(50微摩尔9,11抑制约60%;10,12抑制约50%)和RANK(50微摩尔9,11抑制约85%;50微摩尔10,12抑制约65%)的表达,但对MMP-9或TNFα表达无影响。

结论

9,11 CLA抑制人细胞破骨细胞的形成和活性,表明该异构体可能预防人体的骨吸收。虽然10,12 CLA没有显著减少破骨细胞形成,但它降低了破骨细胞活性以及组织蛋白酶K和RANK的表达,表明该异构体也可能影响骨吸收。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed21/2680857/723a60597877/1476-511X-8-15-1.jpg

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