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Unactivated leukocyte expression of C-reactive protein is minimal and not dependent on rs1205 genotype
C-reactive protein (CRP), a prominent component of the innate immune system, is implicated in the pathophysiology of many conditions. CRP production primarily occurs in the liver; but contributions from other tissues is unclear. The Genotype-Tissue Expression Portal shows essentially no expression i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952394/ https://www.ncbi.nlm.nih.gov/pubmed/33707594 http://dx.doi.org/10.1038/s41598-021-85272-9 |
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author | Best, L. G. Azure, C. Martell, K. Tsosie, K. S. Voels, B. |
author_facet | Best, L. G. Azure, C. Martell, K. Tsosie, K. S. Voels, B. |
author_sort | Best, L. G. |
collection | PubMed |
description | C-reactive protein (CRP), a prominent component of the innate immune system, is implicated in the pathophysiology of many conditions. CRP production primarily occurs in the liver; but contributions from other tissues is unclear. The Genotype-Tissue Expression Portal shows essentially no expression in whole blood and reports in the literature are conflicting. Multiple genomic variants influence serum levels of CRP. We measured CRP mRNA expression in leukocytes and sought to determine if rs1205 genotype influences leukocyte expression. Leukocytes were obtained from 20 women differing by genotype. Quantitative, real-time PCR (RT-qPCR) detected CRP and reference gene (GAPDH) mRNA. Leukocyte expression was calculated by the 2(ΔCT) method, and against a standard curve. Digital drop PCR was also used to calculate expression ratios. Student's t test and linear regression methods examined possible differences between genotypes. During 32 runs (10 replicates each), the RT-qPCR mean (SD) CRP/GAPDH ratio was 3.39 × 10(–4) (SD 1.73 × 10(–4)) and 3.15 × 10(–4) (SD 1.64 × 10(–4)) for TT and CC genotypes respectively, p = 0.76; and digital drop PCR results were similar. Serum CRP was not significantly different between genotypes, nor correlated with leukocyte expression. CRP is minimally expressed in unactivated leukocytes and this expression is not likely influenced by rs1205 genotype. |
format | Online Article Text |
id | pubmed-7952394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79523942021-03-12 Unactivated leukocyte expression of C-reactive protein is minimal and not dependent on rs1205 genotype Best, L. G. Azure, C. Martell, K. Tsosie, K. S. Voels, B. Sci Rep Article C-reactive protein (CRP), a prominent component of the innate immune system, is implicated in the pathophysiology of many conditions. CRP production primarily occurs in the liver; but contributions from other tissues is unclear. The Genotype-Tissue Expression Portal shows essentially no expression in whole blood and reports in the literature are conflicting. Multiple genomic variants influence serum levels of CRP. We measured CRP mRNA expression in leukocytes and sought to determine if rs1205 genotype influences leukocyte expression. Leukocytes were obtained from 20 women differing by genotype. Quantitative, real-time PCR (RT-qPCR) detected CRP and reference gene (GAPDH) mRNA. Leukocyte expression was calculated by the 2(ΔCT) method, and against a standard curve. Digital drop PCR was also used to calculate expression ratios. Student's t test and linear regression methods examined possible differences between genotypes. During 32 runs (10 replicates each), the RT-qPCR mean (SD) CRP/GAPDH ratio was 3.39 × 10(–4) (SD 1.73 × 10(–4)) and 3.15 × 10(–4) (SD 1.64 × 10(–4)) for TT and CC genotypes respectively, p = 0.76; and digital drop PCR results were similar. Serum CRP was not significantly different between genotypes, nor correlated with leukocyte expression. CRP is minimally expressed in unactivated leukocytes and this expression is not likely influenced by rs1205 genotype. Nature Publishing Group UK 2021-03-11 /pmc/articles/PMC7952394/ /pubmed/33707594 http://dx.doi.org/10.1038/s41598-021-85272-9 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Best, L. G. Azure, C. Martell, K. Tsosie, K. S. Voels, B. Unactivated leukocyte expression of C-reactive protein is minimal and not dependent on rs1205 genotype |
title | Unactivated leukocyte expression of C-reactive protein is minimal and not dependent on rs1205 genotype |
title_full | Unactivated leukocyte expression of C-reactive protein is minimal and not dependent on rs1205 genotype |
title_fullStr | Unactivated leukocyte expression of C-reactive protein is minimal and not dependent on rs1205 genotype |
title_full_unstemmed | Unactivated leukocyte expression of C-reactive protein is minimal and not dependent on rs1205 genotype |
title_short | Unactivated leukocyte expression of C-reactive protein is minimal and not dependent on rs1205 genotype |
title_sort | unactivated leukocyte expression of c-reactive protein is minimal and not dependent on rs1205 genotype |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952394/ https://www.ncbi.nlm.nih.gov/pubmed/33707594 http://dx.doi.org/10.1038/s41598-021-85272-9 |
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