scholarly journals The p53 signaling pathway of the large yellow croaker (Larimichthys crocea) responds to acute cold stress: evidence via spatiotemporal expression analysis of p53, p21, MDM2, IGF-1, Gadd45, Fas, and Akt

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e10532
Author(s):  
Baoying Qian ◽  
Xin Qi ◽  
Yi Bai ◽  
Yubo Wu
Keyword(s):  
Cold Stress ◽  
Mrna Expression ◽  
Signaling Pathway ◽  
Environmental Stressors ◽  
Control Group ◽  
Large Yellow Croaker ◽  
Larimichthys Crocea ◽  
Expression Levels ◽  
P53 Signaling ◽  
Cycle Arrest

The p53 activation is induced by stressors, such as DNA damage, oxidative stress, and activated oncogenes, and can promote cell cycle arrest, cellular senescence, and apoptosis. The large yellow croaker (Larimichthys crocea) is an important warm temperate marine fish in the Chinese aquiculture industry. However, few studies have investigated the role of p53 in the response of L. crocea to environmental stressors. Therefore, the aim of the present study was to assess the spatiotemporal mRNA expression levels of genes involved in the p53 signaling pathway of the large yellow croaker in response to cold stress. The results showed significant changes in the expression levels of p53, p21, MDM2, IGF-1, Gadd45, Fas, and Akt in various tissues of the large yellow croaker in response to cold stress for different times. As compared to the control group, p53 mRNA expression was upregulated in most of the examined tissues at 24 h with the exception of the gill. In the liver, the expression levels of p53 and Fas were significantly decreased at 12 h, while those of p21, MDM2, IGF-1, Gadd45 were dramatically increased. Akt expression was notably changed in response to cold in several tissues. These results suggested that p53 was potentially a key gene in the large yellow croaker response to cold and possibly other environmental stressors.

scholarly journals Molecular Characterization and mRNA Expression of ISP2 and ISP4 in the Large Yellow Croaker (Larimichthys Crocea) Under Acute Cold Stress

2021 ◽  
Author(s):  
Baoying Qian
Keyword(s):  
Cold Stress ◽  
Mrna Expression ◽  
Ice Crystals ◽  
Control Group ◽  
Large Yellow Croaker ◽  
Amino Acid Residues ◽  
Larimichthys Crocea ◽  
Warm Temperate ◽  
The Brain ◽  
Different Tissues

Abstract Ice structure proteins (ISPs), also known as antifreeze proteins, can lower the point of freezing by inhibiting the growth of ice crystals and protect organisms from freezing temperatures. The large yellow croaker (Larimichthys crocea) is an important warm-temperate marine fish in Chinese aquaculture. Only a few ISP studies have been reported in this fish to date. In this study, the cDNA of ISP2 were cloned and characterized, and mRNA expression of ISP2 and ISP4 was assessed in different tissues of the large yellow croaker under different periods of acute cold stress (0, 6, 12, 24, 48 and 72 h, rewarming after 12 and 24 h). We found that ISP2 cDNA is 861 bases in length, encoding a protein of 168 amino acid residues. The mRNA expression of ISP2 and ISP4 in tissues of large yellow croaker under different periods of acute cold stress changed significantly. In comparison with the control group, ISP2 expression increased dramatically in the heart (1,976 fold) and intestine (26 fold) after 3 h of acute cold stress and increased 43 fold in the spleen after 6 h. ISP4 expression was up-regulated significantly in the brain (43 fold) and gill (376 fold) at 1 h acute cold stress, and increased 2,774 fold in the intestine at 3 h, 64 fold in muscle and 141 fold in the spleen after rewarming for 1 h after 12 h acute cold stress. These results indicate that ISP2 and ISP4 may play an important role in the response of large yellow croaker to acute cold stress.

Effects of dietary terrestrial oils supplemented with l-carnitine on growth, antioxidant capacity, lipid metabolism and inflammation in large yellow croaker (Larimichthys crocea)

2020 ◽  
pp. 1-11
Author(s):  
Xueshan Li ◽  
Qiang Chen ◽  
Qiuchi Chen ◽  
Kangsen Mai ◽  
Qinghui Ai
Keyword(s):  
Lipid Metabolism ◽  
Antioxidant Capacity ◽  
Mrna Expression ◽  
Lipid Content ◽  
Ldl Cholesterol ◽  
Control Group ◽  
Large Yellow Croaker ◽  
Larimichthys Crocea ◽  
Cpt I ◽  
Hepatic Lipid Content

Abstract The present study was conducted to determine the effects of dietary terrestrial oils (TO) supplemented with l-carnitine on growth performance, biochemical and antioxidant response, lipid metabolism and inflammation in large yellow croaker (Larimichthys crocea). Three iso-nitrogenous and iso-lipidic experimental diets were formulated with FO (fish oil, the control group), 75 % TO (75 % FO was substituted by the oil mixture with equal amounts of soyabean oil, linseed oil and pork lard) and 75 % TOC (75 % TO supplemented with 800 mg/kg l-carnitine). Compared with the control group, feed efficiency ratio and specific growth rate were significantly increased in fish fed diets with 75 % TO and 75 % TOC. Hepatic lipid content, serum TAG level, LDL-cholesterol level and the mRNA expression of pro-inflammatory genes (tnfα and ifnγ) were significantly increased in fish fed the diet with 75 % TO compared with the control group. However, the supplementation of 800 mg/kg l-carnitine in the 75 % TO diet repressed hepatic lipid content, serum LDL-cholesterol level and the mRNA expression of tnfα and ifnγ in fish compared with fish fed the diet with 75 % TO. Total antioxidant capacity, the activity of superoxide dismutase, the mRNA expression of cpt-I and the activity of CPT-I were significantly increased in fish fed the diet with 75 % TOC compared with 75 % TO. In conclusion, these results suggested that the supplementation of 800 mg/kg l-carnitine in the diet with TO mixture could increase growth, antioxidant capacity and fatty acid oxidation and decrease the expression of inflammatory genes in large yellow croaker.

MAVS splicing variants associated with TRAF3 and TRAF6 in NF-κB and IRF3 signaling pathway in large yellow croaker Larimichthys crocea

2021 ◽  
Vol 121 ◽  
pp. 104076
Author(s):  
Peng Fei Zou ◽  
Jun Chun Tang ◽  
Ying Li ◽  
Jian Jun Feng ◽  
Zi Ping Zhang ◽  
...  
Keyword(s):  
Signaling Pathway ◽  
Large Yellow Croaker ◽  
Larimichthys Crocea ◽  
Splicing Variants

scholarly journals Short-term effects of triiodothyronine on thyroid hormone receptor alpha by PI3K pathway in adipocytes, 3T3-L1

2014 ◽  
Vol 58 (8) ◽  
pp. 833-837 ◽  
Author(s):  
Miriane de Oliveira ◽  
Regiane Marques Castro Olimpio ◽  
Maria Teresa De Sibio ◽  
Fernanda Cristina Fontes Moretto ◽  
Renata de Azevedo Mello Luvizotto ◽  
...  
Keyword(s):  
Thyroid Hormone ◽  
Mrna Expression ◽  
Signaling Pathway ◽  
Thyroid Hormone Receptor ◽  
Pi3k Pathway ◽  
Control Group ◽  
Pi3k Signaling ◽  
Pi3k Inhibitor Ly294002 ◽  
Receptor Alpha ◽  
Pi3k Signaling Pathway

Objective The present study aimed to examine the effects of thyroid hormone (TH), more precisely triiodothyronine (T3), on the modulation of TH receptor alpha (TRα) mRNA expression and the involvement of the phosphatidyl inositol 3 kinase (PI3K) signaling pathway in adipocytes, 3T3-L1, cell culture. Materials and methods: It was examined the involvement of PI3K pathway in mediating T3 effects by treating 3T3-L1 adipocytes with physiological (P=10nM) or supraphysiological (SI =100 nM) T3 doses during one hour (short time), in the absence or the presence of PI3K inhibitor (LY294002). The absence of any treatment was considered the control group (C). RT-qPCR was used for mRNA expression analyzes. For data analyzes ANOVA complemented with Tukey’s test was used at 5% significance level. Results T3 increased TRα mRNA expression in P (1.91±0.13, p<0.001), SI (2.14±0.44, p<0.001) compared to C group (1±0.08). This increase was completely abrogated by LY294002 in P (0.53±0.03, p<0.001) and SI (0.31±0.03, p<0.001). To examine whether TRα is directly induced by T3, we used the translation inhibitor cycloheximide (CHX). The presence of CHX completely abrogated levels TRα mRNA in P (1.15±0.05, p>0.001) and SI (0.99±0.15, p>0.001), induced by T3. Conclusion These results demonstrate that the activation of the PI3K signaling pathway has a role in T3-mediated indirect TRα gene expression in 3T3-L1 adipocytes.

scholarly journals Regulation of Free Fatty Acid Receptor 4 on Inflammatory Gene Induced by LPS in Large Yellow Croaker (Larimichthys crocea)

2021 ◽  
Vol 12 ◽  
Author(s):  
Mengjiao Wu ◽  
Qingfei Li ◽  
Kangsen Mai ◽  
Qinghui Ai
Keyword(s):  
Fatty Acid ◽  
Free Fatty Acid ◽  
Mrna Expression ◽  
Head Kidney ◽  
Large Yellow Croaker ◽  
Larimichthys Crocea ◽  
Inflammatory Genes ◽  
Acid Receptor ◽  
Free Fatty Acid Receptor ◽  
Fatty Acid Receptor

Free fatty acid receptor 4 (FFAR4) plays a key role in regulating the inflammatory response in mammals. The present study aimed to investigate the function of large yellow croaker FFAR4 on inflammation. In the present study, ffar4 was widely expressed in 10 tissues of large yellow croaker including gill, head kidney and spleen. Further studies showed that treatment of head kidney macrophages with agonists (TUG891 or GSK137647A) or overexpression of ffar4 reduced the mRNA expression of pro-inflammatory genes induced by LPS, and increased the expression of pparγ. Treatment of macrophages with antagonist AH7614 increased the mRNA expression of pro-inflammatory genes induced by LPS, and decreased the mRNA expression of pparγ. In order to verify the immunomodulatory effect of PPARγ, PPARγ was overexpressed in macrophages which significantly reduced the mRNA expression of pro-inflammatory genes il6, il1β, il8, tnfα and cox2. Moreover, results of dual-luciferase assays showed that PPARγ downregulated the transcriptional activity of il6 and il1β promoters. In conclusion, FFAR4 showed anti-inflammatory effects on LPS-induced inflammation in large yellow croaker.

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