scholarly journals Variants in the CYP2B6 3′UTR Alter In Vitro and In Vivo CYP2B6 Activity: Potential Role of MicroRNAs

2017 ◽  
Vol 104 (1) ◽  
pp. 130-138 ◽  
Author(s):  
Kimberly S. Burgess ◽  
Joseph Ipe ◽  
Marelize Swart ◽  
Ingrid F. Metzger ◽  
Jessica Lu ◽  
...  
Keyword(s):  
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Judit Gil-Zamorano ◽  
João Tomé-Carneiro ◽  
María-Carmen Lopez de las Hazas ◽  
Lorena del Pozo-Acebo ◽  
M. Carmen Crespo ◽  
...  

Abstract The role of miRNAs in intestinal lipid metabolism is poorly described. The small intestine is constantly exposed to high amounts of dietary lipids, and it is under conditions of stress that the functions of miRNAs become especially pronounced. Approaches consisting in either a chronic exposure to cholesterol and triglyceride rich diets (for several days or weeks) or an acute lipid challenge were employed in the search for intestinal miRNAs with a potential role in lipid metabolism regulation. According to our results, changes in miRNA expression in response to fat ingestion are dependent on factors such as time upon exposure, gender and small intestine section. Classic and recent intestinal in vitro models (i.e. differentiated Caco-2 cells and murine organoids) partially mirror miRNA modulation in response to lipid challenges in vivo. Moreover, intestinal miRNAs might play a role in triglyceride absorption and produce changes in lipid accumulation in intestinal tissues as seen in a generated intestinal Dicer1-deletion murine model. Overall, despite some variability between the different experimental cohorts and in vitro models, results show that some miRNAs analysed here are modulated in response to dietary lipids, hence likely to participate in the regulation of lipid metabolism, and call for further research.


2002 ◽  
Vol 57 (5) ◽  
pp. 691-697 ◽  
Author(s):  
Jean Pierre Bercovici ◽  
Veronique Machelon ◽  
Françoise Gaudin-Nome ◽  
Nathalie Roudaut ◽  
Virginie Conan-Charlet ◽  
...  

PLoS ONE ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. e0245166
Author(s):  
Al Shaimaa Hasan ◽  
Lan Luo ◽  
Satoko Baba ◽  
Tao-Sheng Li

Compared to the age-matched men, the incidence of cardiovascular diseases is lower in premenopausal but higher in postmenopausal women, suggesting the cardio-protective role of estrogen in females. Although cardiac stem cells (CSCs) express estrogen receptors, yet the effects of estrogen on CSCs remain unclear. In this study, we investigated the potential role of estrogen in maintaining the quality of CSCs by in vivo and in vitro experiments. For the in vivo study, estrogen deficiency was induced by ovariectomy in 6-weeks-old C57BL/6 female mice, and then randomly given 17β-estradiol (E2) replacements at a low dose (0.01 mg/60 days) and high dose (0.18 mg/60 days), or vehicle treatment. All mice were killed 2 months after treatments, and heart tissues were collected for ex vivo expansion of CSCs. Compared to age-matched healthy controls, estrogen deficiency slightly decreased the yield of CSCs with significantly lower telomerase activity and more DNA damage. Interestingly, E2 replacements at low and high doses significantly increased the yield of CSCs and reversed the quality impairment of CSCs following estrogen deficiency. For the in vitro study, twice-passaged CSCs from the hearts of adult healthy female mice were cultured with the supplement of 0.01, 0.1, and 1 μM E2 in the medium for 3 days. We found that E2 supplement increased c-kit expression, increased proliferative activity, improved telomerase activity, and reduced DNA damage of CSCs in a dose-dependent manner. Our data suggested the potential role of estrogen in maintaining the quality of CSCs, providing new insight into the cardio-protective effects of estrogen.


HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1128d-1128
Author(s):  
Douglas D. Archbold ◽  
Thomas R. Hamilton-Kemp ◽  
John H. Loughrin

Volatile compounds, commonly produced by flowers during bloom, have been described as insect attractants. Some of these compounds stimulate Pinus pollen germination in vitro (French et al., 1979, J. Agric. Fd. Chem., 27184-187), suggesting that such compounds may do the same in vivo. Red Delicious apple pollen was germinated on agar in a simple, enclosed in vitro bioassay system in the presence of a number of plant tissues, including apple, tomato, and chrysanthemum leaves, apple flowers, rose petals, and apple fruit slices. These tissues represent a diversity of types of volatile compounds, Pollen germination was recorded by microphotography after 1 and 2 hours, and percent germination was determined. Although stimulation of germination was not observed, macerated tomato leaves inhibited it. To determine if the volatile characteristics of cultivars differ, flowers of Red Delicious and Golden Delicious apple were harvested at full bloom. Their volatiles were collected, identified, and quantitated by capillary GC-MS. Among 8 major compounds common in the two cultivars, several quantitative differences were observed. These results will be discussed in relation to the potential role of volatiles in pollen germination.


Endocrinology ◽  
2021 ◽  
Vol 163 (1) ◽  
Author(s):  
Cristian A Carvajal ◽  
Alejandra Tapia-Castillo ◽  
Jorge A Pérez ◽  
Carlos E Fardella

Abstract Primary aldosteronism (PA) is an endocrine related condition leading to arterial hypertension due to inappropriately high and unregulated aldosterone concentration. Recently, a broad spectrum of PA has been recognized, which brings new challenges associated with early identification of this condition that affect renal epithelial and extrarenal tissues. Reports have shown the potential role of extracellular vesicles (EVs) and EV cargo as novel and complementary biomarkers in diagnosis and prognosis of PA. In vivo and in vitro studies have identified specific EV surface antigens, EV-proteins, and EV microRNAs that can be useful to develop novel diagnostic algorithms to detect, confirm, or follow up the PA. Moreover, the study of EVs in the field of PA provides further insight in the pathophysiological mechanism of the PA disease.


2012 ◽  
Vol 287 (42) ◽  
pp. 35747-35755 ◽  
Author(s):  
Tanmay Dutta ◽  
Arun Malhotra ◽  
Murray P. Deutscher
Keyword(s):  
X Ray ◽  
E Coli ◽  
Phage T4 ◽  
A Cell ◽  

Escherichia coli RNase BN, a member of the RNase Z family of endoribonucleases, differs from other family members in that it also can act as an exoribonuclease in vitro. Here, we examine whether this activity of RNase BN also functions in vivo. Comparison of the x-ray structure of RNase BN with that of Bacillus subtilis RNase Z, which lacks exoribonuclease activity, revealed that RNase BN has a narrower and more rigid channel downstream of the catalytic site. We hypothesized that this difference in the putative RNA exit channel might be responsible for the acquisition of exoribonuclease activity by RNase BN. Accordingly, we generated several mutant RNase BN proteins in which residues within a loop in this channel were converted to the corresponding residues present in B. subtilis RNase Z, thus widening the channel and increasing its flexibility. The resulting mutant RNase BN proteins had reduced or were essentially devoid of exoribonuclease activity in vitro. Substitution of one mutant rbn gene (P142G) for wild type rbn in the E. coli chromosome revealed that the exoribonuclease activity of RNase BN is not required for maturation of phage T4 tRNA precursors, a known specific function of this RNase. On the other hand, removal of the exoribonuclease activity of RNase BN in a cell lacking other processing RNases leads to slower growth and affects maturation of multiple tRNA precursors. These findings help explain how RNase BN can act as both an exo- and an endoribonuclease and also demonstrate that its exoribonuclease activity is capable of functioning in vivo, thus widening the potential role of this enzyme in E. coli.


2020 ◽  
Vol 11 (19) ◽  
pp. 2915-2934 ◽  
Author(s):  
Gabriela Henríquez ◽  
Alejandra Gomez ◽  
Erick Guerrero ◽  
Mahesh Narayan

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