MiR-16a Regulates Milk Fat Metabolism by Targeting Large Tumor Suppressor Kinase 1 (LATS1) in Bovine Mammary Epithelial Cells

2019 ◽  
Vol 67 (40) ◽  
pp. 11167-11178 ◽  
Author(s):  
Zhi Chen ◽  
Shuangfeng Chu ◽  
Xiaolong Wang ◽  
Yujia Sun ◽  
Tianle Xu ◽  
...  
Keyword(s):  
Tumor Suppressor ◽  
Epithelial Cells ◽  
Milk Fat ◽  
Mammary Epithelial Cells ◽  
Fat Metabolism ◽  
Mammary Epithelial ◽  
Large Tumor ◽  
Bovine Mammary Epithelial Cells ◽  
Large Tumor Suppressor

scholarly journals The effect of short/branched chain acyl-coenzyme A dehydrogenase gene on triglyceride synthesis of bovine mammary epithelial cells

2018 ◽  
Vol 61 (1) ◽  
pp. 115-122 ◽  
Author(s):  
Ping Jiang ◽  
Xibi Fang ◽  
Zhihui Zhao ◽  
Xianzhong Yu ◽  
Boxing Sun ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Dairy Cattle ◽  
Milk Fat ◽  
Mammary Epithelial Cells ◽  
Fat Metabolism ◽  
Mammary Epithelial ◽  
Differentially Expressed ◽  
Bovine Mammary Epithelial Cells ◽  
Chain Acyl ◽  
Branched Chain

Abstract. Short/branched chain acyl-CoA dehydrogenase (ACADSB) is a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids. Our previous transcriptome analysis in dairy cattle showed that ACADSB was differentially expressed and was associated with milk fat metabolism. The aim of this study was to elucidate the background of this differential expression and to evaluate the role of ACADSB as a candidate for fat metabolism in dairy cattle. After analysis of ACADSB mRNA abundance by qRT-PCR and Western blot, overexpression and RNA interference (RNAi) vectors of ACADSB gene were constructed and then transfected into bovine mammary epithelial cells (bMECs) to examine the effects of ACADSB on milk fat synthesis. The results showed that the ACADSB was differentially expressed in mammary tissue of low and high milk fat dairy cattle. Overexpression of ACADSB gene could significantly increase the level of intracellular triglyceride (TG), while ACADSB gene knockdown could significantly reduce the TG synthesis in bMECs. This study suggested that the ACADSB was important in TG synthesis in bMECs, and it could be a candidate gene to regulate the metabolism of milk fat in dairy cattle.

ADIPOR1 regulates genes involved in milk fat metabolism in goat mammary epithelial cells

2021 ◽  
Author(s):  
Wangsheng Zhao ◽  
Michael Adjei ◽  
Hongmei Wang ◽  
Yueling Yangliu ◽  
Jiangjiang Zhu ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Milk Fat ◽  
Mammary Epithelial Cells ◽  
Fat Metabolism ◽  
Mammary Epithelial ◽  
Goat Mammary Epithelial Cells

Effects of Insulin on Milk Fat Synthesis by Regulating the Expressions of SREBP1 and mTOR in Bovine Mammary Epithelial Cells

2020 ◽  
Author(s):  
Nan Li ◽  
Peng-Xia Zhang ◽  
Xin Huang ◽  
Hai-Tao Yao ◽  
Dong-Pu Liu ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Milk Fat ◽  
Mammary Epithelial Cells ◽  
Mammary Epithelial ◽  
Blank Group ◽  
Bovine Mammary Epithelial Cells ◽  
Real Time Quantitative Pcr ◽  
Notable Increase ◽  
Fat Synthesis ◽  
Milk Fat Synthesis

Due to the complexity of insulin in life activities, the role of insulin in mammalian lactation has not been well explained. To investigate the influence of insulin on milk fat synthesis, bovine mammary epithelial cells (BMECs) were cultured in treatment with insulin. We determined the content of Triglyceride (TG) in cell-free culture medium and found a notable increase in TG secrection. Lipid droplet staining study showed a consistent result. We also used real-time quantitative PCR and western blotting to detect the expression of signaling molecules related to milk fat synthesis. We found that insulin resulted in an obvious increase of SREBP-1, mTOR and lipogenic gene expression compared with the blank group. Taken together, our study reveals that insulin plays a significant role in milk fat synthesis.

scholarly journals MiR-485 targets the DTX4 gene to regulate milk fat synthesis in bovine mammary epithelial cells

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Juan Liu ◽  
Ping Jiang ◽  
Ambreen Iqbal ◽  
Shaokat Ali ◽  
Zhen Gao ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Milk Fat ◽  
Target Gene ◽  
Mammary Epithelial Cells ◽  
Cholesterol Content ◽  
Mammary Epithelial ◽  
Bovine Mammary Epithelial Cells ◽  
Candidate Target Gene ◽  
Fat Synthesis ◽  
Milk Fat Synthesis

AbstractMicroRNAs (miRNAs) are mRNA suppressors that regulate a variety of cellular and physiological processes, including cell proliferation, apoptosis, triglyceride synthesis, fat formation, and lipolysis, by post-transcriptional processing. In previous studies, we isolated and sequenced miRNAs from mammary epithelial cells from Chinese Holstein cows with high and low milk fat percentages. MiR-485 was one of the significantly differentially expressed miRNAs that were identified. In the present study, the relationship between the candidate target gene DTX4 and miR-485 was validated by bioinformatics and real-time fluorescent quantitative PCR (qRT-PCR) and Western blot (WB) analyses in bovine mammary epithelial cells (bMECs). The results indicated that miR-485 negatively regulated the mRNA expression of the target gene DTX4. Furthermore, an shRNA interference vector for the target gene DTX4 was constructed successfully, and it increased the triglyceride content and reduced the cholesterol content of transfected cells. These results suggest that miR-485 may affect the contents of triglycerides (TGs) and cholesterol (CHOL) by targeting the DTX4 gene. This study indicates that miR-485 has a role in regulating milk fat synthesis and that miR-485 targets the DTX4 gene to regulate lipid metabolism in bMECs. These findings contribute to the understanding of the functional significance of miR-485 in milk fat synthesis.

scholarly journals Comparative proteome analysis reveals VPS28 regulates milk fat synthesis through ubiquitylation in bovine mammary epithelial cells

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e9542
Author(s):  
Lily Liu ◽  
Qin Zhang
Keyword(s):  
Epithelial Cells ◽  
Milk Fat ◽  
Mammary Epithelial Cells ◽  
Proteome Analysis ◽  
Mammary Epithelial ◽  
Absolute Quantitation ◽  
Bovine Mammary Epithelial Cells ◽  
Fat Synthesis ◽  
Vacuolar Protein ◽  
Milk Fat Synthesis

In our previous study, we found that VPS28 (vacuolar protein sorting 28 homolog) could alter ubiquitylation level to regulate milk fat synthesis in bovine primary mammary epithelial cells (BMECs). While the information on the regulation of VPS28 on proteome of milk fat synthesis is less known, we explored its effect on milk fat synthesis using isobaric tags for relative and absolute quantitation assay after knocking down VPS28 in BMECs. A total of 2,773 proteins in three biological replicates with a false discovery rate of less than 1.2% were identified and quantified. Among them, a subset of 203 proteins were screened as significantly down-(111) and up-(92) regulated in VPS28 knockdown BMECs compared with the control groups. According to Gene Ontology analysis, the differentially expressed proteins were enriched in the “proteasome,” “ubiquitylation,” “metabolism of fatty acids,” “phosphorylation,” and “ribosome.” Meanwhile, some changes occurred in the morphology of BMECs and an accumulation of TG (triglyceride) and dysfunction of proteasome were identified, and a series of genes associated with milk fat synthesis, ubiquitylation and proteasome pathways were analyzed by quantitative real-time PCR. The results of this study suggested VPS28 regulated milk fat synthesis was mediated by ubiquitylation; it could be an important new area of study for milk fat synthesis and other milk fat content traits in bovine.

Sign in / Sign up

Export Citation Format

Share Document