Literature DB >> 33659363

Flow Cytometry of CD14, VDR, Cyp27 and Cyp24 and TLR4 in U937 Cells.

Jacqueline Ferritto Rebello1, Rodrigo Barbosa de Oliveira Brito1, Caren Cristina Grabulosa1, Rosa Maria Affonso Moyses2, Rosilene Motta Elias1,2, Maria Aparecida Dalboni1.   

Abstract

Chronic Kidney Disease (CKD) patients present a micro inflammation state due to failure renal function. The calcitriol has been described as an anti-inflammatory factor that might modulates the inflammatory response in CKD patients. However, these patients have deficiency of Calcitriol due to failure renal function. But, synthesis of this vitamin has been reported in extra renal production, as in monocytes. In this context, it has been reported that the supplementation with 25 vitamin D (calcidiol or inactive form of vitamin D) induces monocytes to downregulate inflammation, due to the intracellular 1α-hidroxilase that converts calcidiol to calcitriol in these cells. Besides some reports used RT-qPCR, Western Blot or immunofluorescence techniques to investigate the expression of inflammatory and vitamin D machinery biomarkers in several disease, in the present study we used flow cytometry technique to evaluate the effect of 25 vitamin D on CD14, Toll-like receptor 4 (TLR4), vitamin D receptor (VDR), 1-α hydroxylase (CYP27), 24 hydroxylase (CYP24) in monocytes lineage (U937). The U937 culture was incubated with healthy or CKD serum and treatment with/without 25-vitamin D (50 ng/ml for 24 h) to evaluate CD14, TRL4, VDR, CYP27 and CYP24 expression. This protocol showed the advantage to investigate the effect of treatment with 25 vitamin D on the intracellular and cell membrane biomarkers expression quickly and simultaneously. In addition, this technique is not laborious, but easy to perform and to interpret compared to RT-qPCR, western blot or immunofluorescence.
Copyright © 2020 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  25 vitamin D; Inflammation; Monocyte lineage (U937); Receptor vitamin D; TLR4

Year:  2020        PMID: 33659363      PMCID: PMC7842305          DOI: 10.21769/BioProtoc.3695

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  27 in total

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Journal:  J Biol Regul Homeost Agents       Date:  2019 Nov-Dec       Impact factor: 1.711

Review 4.  Altered microbiome in chronic kidney disease: systemic effects of gut-derived uremic toxins.

Authors:  Wei Ling Lau; Javad Savoj; Michael B Nakata; Nosratola D Vaziri
Journal:  Clin Sci (Lond)       Date:  2018-03-09       Impact factor: 6.124

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Authors:  Michael F Holick
Journal:  Rheum Dis Clin North Am       Date:  2012-04-12       Impact factor: 2.670

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Authors:  Cynthia Aranow
Journal:  J Investig Med       Date:  2011-08       Impact factor: 2.895

7.  Protein-Bound Uremic Toxins from Gut Microbiota and Inflammatory Markers in Chronic Kidney Disease.

Authors:  Natália A Borges; Amanda F Barros; Lia S Nakao; Carla J Dolenga; Denis Fouque; Denise Mafra
Journal:  J Ren Nutr       Date:  2016-11       Impact factor: 3.655

8.  Indoxyl sulfate upregulates renal expression of ICAM-1 via production of ROS and activation of NF-κB and p53 in proximal tubular cells.

Authors:  Hidehisa Shimizu; Maimaiti Yisireyili; Yukihiro Higashiyama; Fuyuhiko Nishijima; Toshimitsu Niwa
Journal:  Life Sci       Date:  2012-11-28       Impact factor: 5.037

9.  An overview of uremic toxicity.

Authors:  Raymond C Vanholder; Griet L Glorieux
Journal:  Hemodial Int       Date:  2003-04-01       Impact factor: 1.812

10.  Microvesicles Derived from Indoxyl Sulfate Treated Endothelial Cells Induce Endothelial Progenitor Cells Dysfunction.

Authors:  Andres Carmona; Fatima Guerrero; Paula Buendia; Teresa Obrero; Pedro Aljama; Julia Carracedo
Journal:  Front Physiol       Date:  2017-09-08       Impact factor: 4.566

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