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Image Search Results
Journal: EBioMedicine
Article Title: The KLB rs17618244 gene variant is associated with fibrosing MAFLD by promoting hepatic stellate cell activation
doi: 10.1016/j.ebiom.2021.103249
Figure Lengend Snippet: Demographic, anthropometric and clinical features of Hepatology service cohort ( n = 1111) stratified by KLB rs17618244 G > A genotype.
Article Snippet: TaqMan gene assay (
Techniques:
Journal: EBioMedicine
Article Title: The KLB rs17618244 gene variant is associated with fibrosing MAFLD by promoting hepatic stellate cell activation
doi: 10.1016/j.ebiom.2021.103249
Figure Lengend Snippet: Associations between the KLB rs17618244 variant and the independent predictors of liver damage in patients from the Hepatology Service cohort ( n = 1111).
Article Snippet: TaqMan gene assay (
Techniques: Variant Assay
Journal: EBioMedicine
Article Title: The KLB rs17618244 gene variant is associated with fibrosing MAFLD by promoting hepatic stellate cell activation
doi: 10.1016/j.ebiom.2021.103249
Figure Lengend Snippet: The KLB rs17618244 variant is associated with fibrosis in patients with MAFLD. Association of the KLB rs17618244 variant with steatosis ( a ), lobular inflammation ( b ) ballooning grade ( c ) and fibrosis stage ( d ) in MAFLD patients from the Hepatology service cohort ( n = 1111). Multivariable ordinal regression analysis adjusted for age, sex, BMI, T2D, presence of PNPLA3 I148M, TM6SF2 E167K and MBOAT7 T alleles at additive model.
Article Snippet: TaqMan gene assay (
Techniques: Variant Assay
Journal: EBioMedicine
Article Title: The KLB rs17618244 gene variant is associated with fibrosing MAFLD by promoting hepatic stellate cell activation
doi: 10.1016/j.ebiom.2021.103249
Figure Lengend Snippet: The KLB rs17618244 variant is associated with lobular inflammation and fibrosis in patients with obese MAFLD patients. Association of the KLB rs17618244 variant with steatosis, lobular inflammation, ballooning grade and fibrosis stage in MAFLD patients from the Hepatology service cohort ( n = 1111) stratified according to the absence ( a-d ) or presence ( e-h ) of obesity (BMI>35). Multivariable ordinal regression analysis adjusted for age, sex, BMI, T2D, presence of PNPLA3 I148M, TM6SF2 E167K and MBOAT7 T alleles at additive model.
Article Snippet: TaqMan gene assay (
Techniques: Variant Assay
Journal: EBioMedicine
Article Title: The KLB rs17618244 gene variant is associated with fibrosing MAFLD by promoting hepatic stellate cell activation
doi: 10.1016/j.ebiom.2021.103249
Figure Lengend Snippet: Associations between the allelic risk variants and the independent predictors of liver damage in the Hepatology service cohort stratified according to the presence of obesity ( n = 403 no obese patients and n = 708 obese patients).
Article Snippet: TaqMan gene assay (
Techniques:
Journal: EBioMedicine
Article Title: The KLB rs17618244 gene variant is associated with fibrosing MAFLD by promoting hepatic stellate cell activation
doi: 10.1016/j.ebiom.2021.103249
Figure Lengend Snippet: KLB mRNA levels are higher in patients who carry the at risk A allele and correlate with the expression of genes involved in fibrogenesis. KLB ( a ) and CYP7A1 ( b ) mRNA levels in carriers of the rs17618244 A allele compared to non-carriers. Correlation analyses between hepatic KLB gene expression and CYP7A1 ( c ), TGF-β ( d ), COL1A1 ( e ) and COL3A1 ( f ) mRNA levels evaluated by transcriptome analysis on liver biopsies ( n = 125). Circulating levels of KLB ( g ) and FGF19 ( h ) in 175 NAFLD adult patients. Bar graphs represents KLB and FGF serum levels stratified according to the presence of the KLB at risk A allele (GG=59; GA/AA=116). Data were logarithmically transformed and analyzed by 2-tailed T-tests, Adjusted * p <0.05.
Article Snippet: TaqMan gene assay (
Techniques: Expressing, Gene Expression, Transformation Assay
Journal: EBioMedicine
Article Title: The KLB rs17618244 gene variant is associated with fibrosing MAFLD by promoting hepatic stellate cell activation
doi: 10.1016/j.ebiom.2021.103249
Figure Lengend Snippet: Analysis of KLB gene/proteinr expression in LX-2 cells under normal or fasting condition. In this experimental setting LX-2 cells were cultured in fasting (0.5% and 2% FBS) or normal medium (10% FBS) for 24 h. Analysis of relative KLB gene expression evaluated by qRT-PCR (a) . Relative expression of KLB protein levels against α-tubulin determined by densitometric analysis of Western blots. The intensity of the bands was analyzed by ImageJ software (b) . Representative immunofluorescence images of cellular distribution of KLB (green) and αSMA (red). Nuclei are reported in blue. Magnification 60X (c) . Cell proliferation evaluated by a BrdU incorporation and expressed as Europium (Eu) counts (d) . Expressions of αSMA, TGF-β, COL1A1 and COL3A1 genes were measured by qRT-PCR (e) . Data are the mean ± SD of 2 independent experiments repeated at least in triplicate. Data were analyzed by 2-tailed t tests, Adjusted * p <0.05; ** p <0.01; *** p <0.001.
Article Snippet: TaqMan gene assay (
Techniques: Expressing, Cell Culture, Gene Expression, Quantitative RT-PCR, Western Blot, Software, Immunofluorescence, BrdU Incorporation Assay
Journal: EBioMedicine
Article Title: The KLB rs17618244 gene variant is associated with fibrosing MAFLD by promoting hepatic stellate cell activation
doi: 10.1016/j.ebiom.2021.103249
Figure Lengend Snippet: Analysis of the effect of wild-type and mutant KLB overexpression in LX-2 cells. In this experimental setting LX-2 cells were transiently transfected with pCMV6 plasmid (LX-2_Vector), KLB wild-type plasmid (LX-2_KLBwt), or KLB mutant plasmid (LX-2_KLBmut), and all analyses were performed after 48 h. Relative expression of KLB protein levels was determined by densitometric analysis of Western blots. The intensity of the bands was analyzed by ImageJ software (a) . Representative immunofluorescence images of cellular distribution of KLB (green) and αSMA (red). Nuclei are reported in blue. Magnification 60X (b) . Multiple sequence alignment around the site of the Arg728Gln variant among orthologues of KLB and the human Klotho paralogue. Consensus and similar residues are respectively in black and gray background. The consensus residues NxS/T (where “x” can be any residue except proline) for the N-glycosylation of Asn611 are indicated (c) . The structure of the KLB GH2 domain isolated from the Protein Data Bank entry 5VAN and the modelled to show the position of Arg728, the N-glycosylable Asn611 (d) . Same KLB GH2 domain structure as in D represented as molecular surface colored by residue hydrophobicity, highlighting the surface-exposed protein hydrophobic patch (left) and showing a modelled mannose(x3)-GlcNAc(x2) glycan N-linked to Asn611 ( e ). Cell proliferation was evaluated by a BrdU incorporation kit and expressed as Eu counts ( f ). mRNA levels of αSMA, TGF-β, COL1A1 and COL3A1 were evaluated by qRT-PCR (g) . Hypothesis of mechanism by which KLB exert the inhibition of pro-fibrogenic genes after LX-2 cells stimulation with FGF19 ( h ). mRNA levels of SHP-1 and COL1A1 were evaluated by qRT-PCR ( i ). Representative immunofluorescence images of cellular distribution of SMAD3 (red). Magnification 40X ( j) . Quantitative data are the mean ± SD of 2 independent experiments repeated at least in triplicate. Data were analyzed by two-way ANOVA with Bonferroni post hoc test for multiple comparisons. Adjusted * p <0.05; ** p <0.01; *** p <0.001.
Article Snippet: TaqMan gene assay (
Techniques: Mutagenesis, Over Expression, Transfection, Plasmid Preparation, Expressing, Western Blot, Software, Immunofluorescence, Sequencing, Variant Assay, Residue, Glycoproteomics, Isolation, BrdU Incorporation Assay, Quantitative RT-PCR, Inhibition