Relative role of free fatty acids on expression of miR-335 in human matured adipocytes
10.3969/cma.j.issn.2095-428X.2013.19.008
- VernacularTitle:游离脂肪酸对人成熟脂肪细胞中miR-335表达的调控
- Author:
Lu ZHU
1
;
Yan CUI
;
Yu-Hui NI
;
Guang-Feng XU
;
Chun-Mei SHI
;
Xi-Rong GUO
;
Chen-Bo JI
Author Information
1. 210029,南京医科大学护理学院
- Keywords:
MiR-335;
Free fatty acid;
Adipocyte
- From:
Chinese Journal of Applied Clinical Pediatrics
2013;28(19):1464-1466
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the role of free fatty acids(FFA) on expression of miR-335 in human matured adipocytes.Methods In order to induce differentiation,confluent human pre-adipocytes (day 0) were subsequently cultured in serum-free PAM containing 50 nmol/L insulin,100 nmol/L dexamethasone,0.5 mmol/L 3-isobutyl1-methylxanthine,and 100 μmol/L rosiglitazone.Then human matured adipocytes (day 16) were treated with 1 mmol/L FFA cocktail composed of lauric acid,myristic acid,linoleic acid,oleic acid,and arachidonic acids for 4,8 and 24 hours.Meanwhile,untreated cells were collected as control group.Total RNA from these adipocytes were extracted and the levels of miR-335 expression were evaluated by real-time PCR.Results The expression of miR-335 at 4,8 and 24 hours showed no statistical significance when compared to 0 hour in untreated matured adipocytes (all P ＞ 0.05).The relative expression of miR-335 after the intervention of FFA in human matured adipocytes were 9.03 ± 0.31,9.85 ±2.41 and 11.23 ± 0.62,respectively at 4,8 and 24 hours when used with snRU6 for normalization,and there was statistical signi-ficance compared with 0 hour in control group (all P ＜ 0.05).The levels of miR-335 were 4.73 ± 0.60,5.38 ± 1.25 and 4.57 ±0.52 at the same time point when used with miR-103 for normalization,and there was statistical significance compared with 0 hour in control group (all P ＜ 0.05).Conclusions FFA exert a positive effect on the miR-335 expression in human matured adipocytes,which provide the basis for the further study about the role of miR-335 in human adipocytes.
