scholarly journals Molecular Identification and Antibacterial Activity Analysis of Blue Fox (Vulpes lagopus) β-Defensins 108 and 122

Animals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1857
Author(s):  
Ling-Ling Li ◽  
Tao-Lin Liu ◽  
Ping Wu ◽  
Nian-Yan Du ◽  
Li-Hong Tian ◽  
...  
Keyword(s):  
Antibacterial Activity ◽  
Protein Structure ◽  
Semen Quality ◽  
Bacterial Invasion ◽  
Vulpes Lagopus ◽  
Reproductive Process ◽  
Key Factor ◽  
Blue Fox ◽  
And Function

The blue fox (Vulpes lagopus), a fur-bearing animal, is an important component of the breeding industry in China. Semen quality is a key factor for the reproductive process and the breeding effectiveness of the farmed blue fox. However, bacterial contamination in semen samples utilized in artificial fertilization is very common. The β-defensins, a class of important antimicrobial peptides in mammals, could protect the reproductive system of male animals from bacterial invasion, maintain the stability of the genital tract microenvironment and improve semen quality. In this study, molecular cloning and bioinformatics analysis were conducted to analyze the protein structure and function of blue fox β-defensin 108 (Vulpes lagopus beta-defensin 108, vBD108) and 122 (Vulpes lagopus beta-defensin 122, vBD122). To evaluate the bacteriostatic effect of recombinant vBDs (Vulpes lagopus beta-defensins) protein, varying concentrations (0, 25, 50, 100, 200 µg/mL) were taken to evaluate the effects on Escherichia coli and Staphylococcus aureus at different times (0, 2, 4, 6, 8, 12 h). The results showed that vBD108 and vBD122 existed in different forms in protein structure and had antibacterial activity. Both proteins, at 50 µg/mL, had efficacious bacteriostatic activity. This study shows that recombinant vBD108 and vBD122 proteins have good antibacterial activity in vitro. This implies a potential role in improving semen quality and hygienic measures in the process of artificial insemination as an extender of semen dilution with antibacterial activity.

Silencing of NHE-1 blunts the slow force response to myocardial stretch

2011 ◽  
Vol 111 (3) ◽  
pp. 874-880 ◽  
Author(s):  
Néstor G. Pérez ◽  
Mariela B. Nolly ◽  
Mirian C. Roldan ◽  
María C. Villa-Abrille ◽  
Eugenio Cingolani ◽  
...  
Keyword(s):  
Lentiviral Vector ◽  
Ventricular Myocardium ◽  
Left Ventricular ◽  
Left Ventricular Myocardium ◽  
Force Response ◽  
Rapid Phase ◽  
Key Factor ◽  
Myocardial Stretch ◽  
And Function

Myocardial stretch induces a biphasic force response: a first abrupt increase followed by a slow force response (SFR), believed to be the in vitro manifestation of the Anrep effect. The SFR is due to an increase in Ca2+ transient of unclear mechanism. We proposed that Na+/H+ exchanger (NHE-1) activation is a key factor in determining the contractile response, but recent reports challenged our findings. We aimed to specifically test the role of the NHE-1 in the SFR. To this purpose small hairpin interference RNA capable of mediating specific NHE-1 knockdown was incorporated into a lentiviral vector (l-shNHE1) and injected into the left ventricular wall of Wistar rats. Injection of a lentiviral vector expressing a nonsilencing sequence (scramble) served as control. Myocardial NHE-1 protein expression and function (the latter evaluated by the recovery of pHi after an acidic load and the SFR) were evaluated. Animals transduced with l-shNHE1 showed reduced NHE-1 expression (45 ± 8% of controls; P < 0.05), and the presence of the lentivirus in the left ventricular myocardium, far from the site of injection, was evidenced by confocal microscopy. These findings correlated with depressed basal pHi recovery after acidosis [maxdpHi/d t 0.055 ± 0.008 (scramble) vs. 0.009 ± 0.004 (l-shNHE1) pH units/min, P < 0.05], leftward shift of the relationship between JH+ (H+ efflux corrected by the intrinsic buffer capacity), and abolishment of SFR (124 ± 2 vs. 101 ± 2% of rapid phase; P < 0.05) despite preserved ERK1/2 phosphorylation [247 ± 12 (stretch) and 263 ± 23 (stretch l-shNHE1) % of control; P < 0.05 vs. nonstretched control], well-known NHE-1 activators. Our results provide strong evidence to propose NHE-1 activation as key factor in determining the SFR to stretch.

11 Metal Amino Acid Chelates/complexes with Emphasis on Molecule Absorption and Efficacy Differences in Swine

2021 ◽  
Vol 99 (Supplement_1) ◽  
pp. 14-14
Author(s):  
Karen J Wedekind
Keyword(s):  
Molecular Structures ◽  
Trace Minerals ◽  
Immune Development ◽  
Biochemical Processes ◽  
Sow Longevity ◽  
Organic Trace Minerals ◽  
Key Factor ◽  
And Function

Abstract The objective of this presentation will be to discuss differences in the molecular structures between various organic trace minerals (OTM) and inorganic trace minerals (ITM) and discuss how these properties impact stability, absorption, bioavailability and retention. The Association of American Feed Control Officials (AAFCO) lists several different categories of OTM including chelates, complexes and proteinates. Typical ligands include organic acids, amino acids, peptides and polysaccharides. It is widely known that bioavailability of ITM is low, primarily due to the presence of antagonisms such as phytate and/or fiber or excesses of other minerals. For this reason, inclusions of trace minerals (e.g. Zn, Cu, Mn, Fe) are often added in commercial livestock diets at 2–3-fold higher concentrations than recommended by NRC. Feeding highly bioavailable trace minerals is important. These minerals are required components of thousands of the proteins, enzymes and transcription factors that support a wide variety of biochemical processes in the cells and tissues of animals. These functions include gene regulation, cell growth and division, immune development and function, tissue development and integrity, reproduction and oxidative stress management. Low bioavailability of these trace minerals can reduce animal performance, immune function, reproductive performance and increase lameness. Numerous in vitro and in vivo methodologies have been used to compare bioavailability and demonstrate higher stability, tissue retention and digestibility of OTM vs ITM. Sow longevity is a key factor in commercial swine herd profitability. Reproductive problems and lameness are the most common reasons for premature sow culling from breeding herds. Compared to ITM, OTM reduced gilt and sow mortality 9–17% (P &lt; 0.10), culling rate 20–35% (P &lt; 0.01) and increased sow retention (through parity 3) 5–10%; (P &lt; 0.01). Greater bioavailability translates to biological benefits to the producer, however, our findings demonstrate that not all OTM perform better than ITM.

Molecular architecture and functions of the neuronal cytoskeleton

1990 ◽  
Vol 48 (3) ◽  
pp. 2-3
Author(s):  
Nobutaka Hirokawa
Keyword(s):  
Major Elements ◽  
Molecular Structures ◽  
Organelle Transport ◽  
Molecular Architecture ◽  
Neuronal Morphogenesis ◽  
Microtubule Associated Proteins ◽  
Associated Proteins ◽  
And Function ◽  
Small Clusters

In this symposium I will present our studies about the molecular architecture and function of the cytomatrix of the nerve cells. The nerve cell is a highly polarized cell composed of highly branched dendrites, cell body, and a single long axon along the direction of the impulse propagation. Each part of the neuron takes characteristic shapes for which the cytoskeleton provides the framework. The neuronal cytoskeletons play important roles on neuronal morphogenesis, organelle transport and the synaptic transmission. In the axon neurofilaments (NF) form dense arrays, while microtubules (MT) are arranged as small clusters among the NFs. On the other hand, MTs are distributed uniformly, whereas NFs tend to run solitarily or form small fascicles in the dendrites Quick freeze deep etch electron microscopy revealed various kinds of strands among MTs, NFs and membranous organelles (MO). These structures form major elements of the cytomatrix in the neuron. To investigate molecular nature and function of these filaments first we studied molecular structures of microtubule associated proteins (MAP1A, MAP1B, MAP2, MAP2C and tau), and microtubules reconstituted from MAPs and tubulin in vitro. These MAPs were all fibrous molecules with different length and formed arm like projections from the microtubule surface.

Role of the 807 C/T Polymorphism of the α2 Gene in Platelet GP Ia Collagen Receptor Expression and Function

1999 ◽  
Vol 81 (06) ◽  
pp. 951-956 ◽  
Author(s):  
J. Corral ◽  
R. González-Conejero ◽  
J. Rivera ◽  
F. Ortuño ◽  
P. Aparicio ◽  
...  
Keyword(s):  
Venous Thrombosis ◽  
Cell Types ◽  
Receptor Expression ◽  
Case Control Studies ◽  
Platelet Surface ◽  
Vitro Analysis ◽  
And Function ◽  
In Vitro Analysis

SummaryThe variability of the platelet GP Ia/IIa density has been associated with the 807 C/T polymorphism (Phe 224) of the GP Ia gene in American Caucasian population. We have investigated the genotype and allelic frequencies of this polymorphism in Spanish Caucasians. The T allele was found in 35% of the 284 blood donors analyzed. We confirmed in 159 healthy subjects a significant association between the 807 C/T polymorphism and the platelet GP Ia density. The T allele correlated with high number of GP Ia molecules on platelet surface. In addition, we observed a similar association of this polymorphism with the expression of this protein in other blood cell types. The platelet responsiveness to collagen was determined by “in vitro” analysis of the platelet activation and aggregation response. We found no significant differences in these functional platelet parameters according to the 807 C/T genotype. Finally, results from 3 case/control studies involving 302 consecutive patients (101 with coronary heart disease, 104 with cerebrovascular disease and 97 with deep venous thrombosis) determined that the 807 C/T polymorphism of the GP Ia gene does not represent a risk factor for arterial or venous thrombosis.

Type I Interferons promote maintenance and function of follicular T helper cells in vitro

2019 ◽  
Author(s):  
S Ehrlich ◽  
K Wild ◽  
M Smits ◽  
K Zoldan ◽  
M Hofmann ◽  
...  
Keyword(s):  
T Helper Cells ◽  
Type I Interferons ◽  
Type I ◽  
T Helper ◽  
Helper Cells ◽  
Follicular T Helper Cells ◽  
And Function
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