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本文引用的文献

1
Antenatal taurine supplementation in fetal rats with growth restriction improves neural stem cell proliferation by inhibiting the activities of Rho family factors.孕期补充牛磺酸可改善生长受限胎鼠的神经干细胞增殖,其机制是通过抑制Rho家族因子的活性。
J Matern Fetal Neonatal Med. 2018 Jun;31(11):1454-1461. doi: 10.1080/14767058.2017.1319353. Epub 2017 May 5.
2
[Effect of antepartum taurine supplementation in regulating the activity of Rho family factors and promoting the proliferation of neural stem cells in neonatal rats with fetal growth restriction].[产前补充牛磺酸对调节胎儿生长受限新生大鼠Rho家族因子活性及促进神经干细胞增殖的作用]
Zhongguo Dang Dai Er Ke Za Zhi. 2016 Nov;18(11):1158-1165. doi: 10.7499/j.issn.1008-8830.2016.11.021.
3
Docosahexaenoic acid up-regulates both PI3K/AKT-dependent FABP7-PPARγ interaction and MKP3 that enhance GFAP in developing rat brain astrocytes.二十二碳六烯酸上调PI3K/AKT依赖性的脂肪酸结合蛋白7(FABP7)-过氧化物酶体增殖物激活受体γ(PPARγ)相互作用以及双特异性磷酸酶3(MKP3),这两者可增强发育中大鼠脑星形胶质细胞中的胶质纤维酸性蛋白(GFAP)。
J Neurochem. 2017 Jan;140(1):96-113. doi: 10.1111/jnc.13879. Epub 2016 Dec 7.
4
Long-Term Effect of Docosahexaenoic Acid Feeding on Lipid Composition and Brain Fatty Acid-Binding Protein Expression in Rats.二十二碳六烯酸喂养对大鼠脂质组成及脑脂肪酸结合蛋白表达的长期影响
Nutrients. 2015 Oct 22;7(10):8802-17. doi: 10.3390/nu7105433.
5
Fatty acid binding protein 7 and n-3 poly unsaturated fatty acid supply in early rat brain development.脂肪酸结合蛋白7与大鼠脑早期发育中的n-3多不饱和脂肪酸供应
Dev Neurobiol. 2016 Mar;76(3):287-97. doi: 10.1002/dneu.22314. Epub 2015 Jun 11.
6
Fatty Acid Binding Protein 3 Is Involved in n-3 and n-6 PUFA transport in mouse trophoblasts.脂肪酸结合蛋白3参与小鼠滋养层细胞中n-3和n-6多不饱和脂肪酸的转运。
J Nutr. 2014 Oct;144(10):1509-16. doi: 10.3945/jn.114.197202. Epub 2014 Aug 13.
7
Meeting the fetal requirement for polyunsaturated fatty acids in pregnancy.满足孕期胎儿对多不饱和脂肪酸的需求。
Curr Opin Clin Nutr Metab Care. 2014 Mar;17(2):151-5. doi: 10.1097/MCO.0000000000000036.
8
Fatty acid binding protein 7 as a marker of glioma stem cells.脂肪酸结合蛋白 7 作为神经胶质瘤干细胞的标志物。
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9
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10
A fatty acid-binding protein 7/RXRβ pathway enhances survival and proliferation in triple-negative breast cancer.脂肪酸结合蛋白 7/RXRβ 通路增强三阴性乳腺癌的存活和增殖。
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[FABP7在小鼠胎盘组织和人滋养层细胞HTR-8/Svneo中的表达]

[Expression of FABP7 in mouse placenta tissue and human trophoblast HTR-8/Svneo cells].

作者信息

Tian Liu, Liao Hui-Qi, Yang Hui, Ma Ni, Zhang Chang-Jun, Diao Hong-Lu

机构信息

Reproductive Medicine Center, People's Hospital Affiliated to Hubei University of Medicine, Shiyan 442000, China.E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2017 May 20;37(5):594-599. doi: 10.3969/j.issn.1673-4254.2017.05.05.

DOI:10.3969/j.issn.1673-4254.2017.05.05
PMID:28539280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6780475/
Abstract

OBJECTIVE

To detect the expression of FABP7 in the placenta of pregnant mice and in HTR-8/Svneo cells.

METHODS

Real-time PCR and immunofluorescence were used to detect FABP7 mRNA and protein expressions in the uterine and placental tissue of pregnant mice at different days of gestation. FABP7 expression was also detected in cultured HTR-8/Svneo cells using immunofluorescence assay. The mice were treated with E, P or their combination for 6 and 24 h and Fabp7 mRNA level in the uterus was detected with real-time PCR.

RESULTS

At 7.5-10.5 days of gestation, the pregnant mice showed positive expressions of Fabp7 mRNA in the uterus and placenta, and FABP7 protein was detected in the decidualized cells and trophoblast giant cells. The expressions of FABP7 were detected at both the mRNA and protein levels in cultured HTR-8/Svneo cells. In mice treated with P4 alone or with E+P for 6 and 24 h, the expression level of Fabp7 mRNA was upregulated in the uterus. Fabp7 upregulation was observed in mice at 24 h following E treatment but not at 6 h.

CONCLUSION

FABP7 is expressed in trophoblast giant cells and decidual cells in the placental tissue of mice and in cultured HTR-8/Svneo cells, suggesting the involvement of FABP7 in placental development and in maintenance of pregnancy. E and P can regulate the expression of FABP7 in mouse uterus.

摘要

目的

检测脂肪酸结合蛋白7(FABP7)在妊娠小鼠胎盘及HTR-8/Svneo细胞中的表达。

方法

采用实时荧光定量PCR和免疫荧光法检测不同妊娠天数的妊娠小鼠子宫和胎盘组织中FABP7 mRNA和蛋白的表达。采用免疫荧光法检测培养的HTR-8/Svneo细胞中FABP7的表达。对小鼠分别用雌激素(E)、孕激素(P)或其联合处理6小时和24小时,用实时荧光定量PCR检测子宫中Fabp7 mRNA水平。

结果

在妊娠7.5 - 10.5天时,妊娠小鼠子宫和胎盘中Fabp7 mRNA呈阳性表达,在蜕膜化细胞和滋养层巨细胞中检测到FABP7蛋白。在培养的HTR-8/Svneo细胞中检测到FABP7在mRNA和蛋白水平均有表达。单独用P4或E + P处理小鼠6小时和24小时后,子宫中Fabp7 mRNA表达水平上调。E处理24小时后的小鼠中观察到Fabp7上调,但6小时时未观察到。

结论

FABP7在小鼠胎盘组织的滋养层巨细胞和蜕膜细胞以及培养的HTR-8/Svneo细胞中表达,提示FABP7参与胎盘发育和维持妊娠。E和P可调节小鼠子宫中FABP7的表达。