Cargando…
Sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin
The C-terminal pro-fibrillin-1 propeptide asprosin is described as white adipose tissue derived hormone that stimulates rapid hepatic glucose release and activates hunger-promoting hypothalamic neurons. Numerous studies proposed correlations of asprosin levels with clinical parameters. However, the...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789892/ https://www.ncbi.nlm.nih.gov/pubmed/35079041 http://dx.doi.org/10.1038/s41598-022-05060-x |
_version_ | 1784639877624627200 |
---|---|
author | Morcos, Yousef A. T. Lütke, Steffen Tenbieg, Antje Hanisch, Franz-Georg Pryymachuk, Galyna Piekarek, Nadin Hoffmann, Thorben Keller, Titus Janoschek, Ruth Niehoff, Anja Zaucke, Frank Dötsch, Jörg Hucklenbruch-Rother, Eva Sengle, Gerhard |
author_facet | Morcos, Yousef A. T. Lütke, Steffen Tenbieg, Antje Hanisch, Franz-Georg Pryymachuk, Galyna Piekarek, Nadin Hoffmann, Thorben Keller, Titus Janoschek, Ruth Niehoff, Anja Zaucke, Frank Dötsch, Jörg Hucklenbruch-Rother, Eva Sengle, Gerhard |
author_sort | Morcos, Yousef A. T. |
collection | PubMed |
description | The C-terminal pro-fibrillin-1 propeptide asprosin is described as white adipose tissue derived hormone that stimulates rapid hepatic glucose release and activates hunger-promoting hypothalamic neurons. Numerous studies proposed correlations of asprosin levels with clinical parameters. However, the enormous variability of reported serum and plasma asprosin levels illustrates the need for sensitive and reliable detection methods in clinical samples. Here we report on newly developed biochemical methods for asprosin concentration and detection in several body fluids including serum, plasma, saliva, breast milk, and urine. Since we found that glycosylation impacts human asprosin detection we analyzed its glycosylation profile. Employing a new sandwich ELISA revealed that serum and saliva asprosin correlate strongly, depend on biological sex, and feeding status. To investigate the contribution of connective tissue-derived asprosin to serum levels we screened two cohorts with described cartilage turnover. Serum asprosin correlated with COMP, a marker for cartilage degradation upon running exercise and after total hip replacement surgery. This together with our finding that asprosin is produced by primary human chondrocytes and expressed in human cartilage suggests a contribution of cartilage to serum asprosin. Furthermore, we determined asprosin levels in breast milk, and urine, for the first time, and propose saliva asprosin as an accessible clinical marker for future studies. |
format | Online Article Text |
id | pubmed-8789892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87898922022-01-27 Sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin Morcos, Yousef A. T. Lütke, Steffen Tenbieg, Antje Hanisch, Franz-Georg Pryymachuk, Galyna Piekarek, Nadin Hoffmann, Thorben Keller, Titus Janoschek, Ruth Niehoff, Anja Zaucke, Frank Dötsch, Jörg Hucklenbruch-Rother, Eva Sengle, Gerhard Sci Rep Article The C-terminal pro-fibrillin-1 propeptide asprosin is described as white adipose tissue derived hormone that stimulates rapid hepatic glucose release and activates hunger-promoting hypothalamic neurons. Numerous studies proposed correlations of asprosin levels with clinical parameters. However, the enormous variability of reported serum and plasma asprosin levels illustrates the need for sensitive and reliable detection methods in clinical samples. Here we report on newly developed biochemical methods for asprosin concentration and detection in several body fluids including serum, plasma, saliva, breast milk, and urine. Since we found that glycosylation impacts human asprosin detection we analyzed its glycosylation profile. Employing a new sandwich ELISA revealed that serum and saliva asprosin correlate strongly, depend on biological sex, and feeding status. To investigate the contribution of connective tissue-derived asprosin to serum levels we screened two cohorts with described cartilage turnover. Serum asprosin correlated with COMP, a marker for cartilage degradation upon running exercise and after total hip replacement surgery. This together with our finding that asprosin is produced by primary human chondrocytes and expressed in human cartilage suggests a contribution of cartilage to serum asprosin. Furthermore, we determined asprosin levels in breast milk, and urine, for the first time, and propose saliva asprosin as an accessible clinical marker for future studies. Nature Publishing Group UK 2022-01-25 /pmc/articles/PMC8789892/ /pubmed/35079041 http://dx.doi.org/10.1038/s41598-022-05060-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Morcos, Yousef A. T. Lütke, Steffen Tenbieg, Antje Hanisch, Franz-Georg Pryymachuk, Galyna Piekarek, Nadin Hoffmann, Thorben Keller, Titus Janoschek, Ruth Niehoff, Anja Zaucke, Frank Dötsch, Jörg Hucklenbruch-Rother, Eva Sengle, Gerhard Sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin |
title | Sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin |
title_full | Sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin |
title_fullStr | Sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin |
title_full_unstemmed | Sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin |
title_short | Sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin |
title_sort | sensitive asprosin detection in clinical samples reveals serum/saliva correlation and indicates cartilage as source for serum asprosin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789892/ https://www.ncbi.nlm.nih.gov/pubmed/35079041 http://dx.doi.org/10.1038/s41598-022-05060-x |
work_keys_str_mv | AT morcosyousefat sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT lutkesteffen sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT tenbiegantje sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT hanischfranzgeorg sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT pryymachukgalyna sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT piekareknadin sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT hoffmannthorben sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT kellertitus sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT janoschekruth sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT niehoffanja sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT zauckefrank sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT dotschjorg sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT hucklenbruchrothereva sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin AT senglegerhard sensitiveasprosindetectioninclinicalsamplesrevealsserumsalivacorrelationandindicatescartilageassourceforserumasprosin |