94 A POLARIZED CELL-CULTURE SYSTEM TO STUDY THE EFFECTS OF ELEVATED SERUM NONESTERIFIED FATTY ACID CONCENTRATIONS ON THE BOVINE OVIDUCTAL MICROENVIRONMENT IN VITRO

2013 ◽  
Vol 25 (1) ◽  
pp. 195
Author(s):  
L. Jordaens ◽  
S. Valckx ◽  
V. Van Hoeck ◽  
M. Berth ◽  
P. E. J. Bols ◽  
...  

The detrimental consequences of elevated serum nonesterified fatty acid concentrations (NEFA) typical in negative energy balance, obesity, or type II diabetes have previously been demonstrated in ovarian follicles. However, regardless its key role in reproduction, the consequences of elevated NEFA on oviductal physiology are unclear. Therefore, the aim of this study was to 1) determine whether serum NEFAs can be found in the oviductal microenvironment using a polarized oviductal epithelial cell culture and more specifically to 2) study the effect of the BSA gradient and the direction of the NEFA gradient. Bovine oviductal epithelial cells from slaughterhouse oviducts in Day 3 to 5 of the luteal phase were mechanically isolated and cultured for 7 days in a flask. Cells were transferred in a polarized oviductal epithelial cell culture-system (Snapwell® polyester membrane, pore size 0.4 µm, 4 × 106 pores cm–2) with an apical (A) and basal (B) medium supporting cell growth until the transepithelial electric resistance reached 700 Ωcm2 (Day 6). Then, cells were exposed to a transmembranary BSA (0.75 or 3% BSA) or NEFA gradient (0 or 360 µM NEFA: 115 µM oleic acid, 140 µM stearic acid, 105 µM palmitic acid) for 48 h in 4 experimental setups: 1) A and B containing 0.75% BSA and B supplemented with NEFA, 2) same as in 1 but NEFAs were added in A, 3) A containing 0.75% BSA and B supplemented with 3% BSA and NEFA, 4) same as in 3 but with 3% BSA + NEFA in A and B contained 0.75% BSA. Samples were analyzed for total NEFA and specific fatty-acid concentrations by photometric and gas chromatographic assays. In total, 72 wells in 4 replicates were cultured and analyzed. Data were processed by paired sample t-tests and student t-tests. Exposure to NEFA did not alter the transepithelial electric resistance. In Exp. 1, the total NEFA concentration in A increased with 0.013 µM (21.11%) over 48 h of NEFA exposure in the basal compartment explained by a significant rise of stearic (8.52 µM, 20.68%) and oleic acid (12.86 µM, 45.17%) accompanied with only a 19.45% decrease of total NEFA in B (P < 0.05). When the transport direction was reversed in Exp. 2, the total NEFA concentration decreased 53.4% in A, with no obvious NEFA rise in B. Implementing a BSA gradient (Exp. 3 and 4) was associated with a slight decrease (13 and 15.7%, respectively; P < 0.05) of NEFA concentration in the supplemented compartment, but no obvious NEFA increase in the opposite compartment could be detected. Overall, these results suggest that NEFA transport in this culture system is tightly regulated and can only be influenced by the transport direction of the NEFA. Further research should focus on transport and metabolisation of the fatty acids added.

1993 ◽  
Vol 20 (5) ◽  
pp. 248-256 ◽  
Author(s):  
PRISCILLA B. WYRICK ◽  
CAROLYN H. DAVIS ◽  
STEPHEN T. KNIGHT ◽  
JOHN CHOONG ◽  
JANE E. RAULSTON ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (7) ◽  
pp. e69797 ◽  
Author(s):  
Hanna Lucia Worliczek ◽  
Bärbel Ruttkowski ◽  
Lukas Schwarz ◽  
Kirsti Witter ◽  
Waltraud Tschulenk ◽  
...  

2021 ◽  
Author(s):  
G. Sushma ◽  
P. Jaya Laxmi ◽  
S.T. Viroji Rao ◽  
R.M.V. Prasad ◽  
M. Kanakachari ◽  
...  

Abstract The poultry industry provides cost-effective, healthy, and protein-enriched food for the growing population and achieving the nutritional security to the country. Excessive abdominal and subcutaneous fat deposition is one of the major setbacks to the poultry industry that reduces carcass yield and feed efficiency. In chicken abdominal fat constitutes 20% of total body fat which make up 2–3% of live weight of the bird. In fatty acid metabolism, acetyl-CoA Carboxylase (ACC) is one of the key enzymes with two isoforms i.e. ACACA and ACACB each of which plays a different role. In chicken, ACACB is involved in the β-oxidation of fatty acids and thereby potentially regulating the quality of meat and egg. The RNAi strategy is widely used for silencing the target gene expression. In this study, we designed five shRNA constructs and identified the most efficient shRNA molecule for silencing the ACACB gene under in vitro chicken embryo myoblast (CEM) primary cell culture system. After knocking down the ACACB gene, for understanding how fatty acid metabolism is regulated, we tracked the expression of key fatty acid metabolism genes like ACACA, FASN, SCD, ELOVL2, and CPT1. Also, checked the expression of immune response genes like IFNA, IFNB, and BLB1 in control as well as ACACB knockdown myoblast cells and observed no significant difference. We observed the down-regulation of key fatty acid metabolism genes along with ACACB, which may leads to the less fat accumulation in CEM cells. We also estimated the cholesterol and triglycerides in control and ACACB knockdown myoblast cells and found a significant difference between control and the knockdown cells. In vitro knockdown of the ACACB gene in a cell culture system by a short hairpin RNA (shRNA) expressing construct would help to produce a knockdown chicken with reduced fat deposition.


Sign in / Sign up

Export Citation Format

Share Document