Cargando…

Expression of genes with biomarker potential identified in skin from DSLD-affected horses increases with age

Degenerative Suspensory Ligament Desmitis (DSLD) negatively impacts connective tissues in horses, which often leads to progressive chronic pain and lameness. DSLD has been shown to be a systemic disorder that affects multiple body systems, including tendons, sclerae, and the aorta. Currently, the di...

Descripción completa

Detalles Bibliográficos
Autores principales: Roberts, Jennifer Hope, Zhang, Jian, David, Florent, McLean, Amy, Blumenshine, Karen, Müller-Alander, Eva, Halper, Jaroslava
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348567/
https://www.ncbi.nlm.nih.gov/pubmed/37450486
http://dx.doi.org/10.1371/journal.pone.0287740
_version_ 1785073694271340544
author Roberts, Jennifer Hope
Zhang, Jian
David, Florent
McLean, Amy
Blumenshine, Karen
Müller-Alander, Eva
Halper, Jaroslava
author_facet Roberts, Jennifer Hope
Zhang, Jian
David, Florent
McLean, Amy
Blumenshine, Karen
Müller-Alander, Eva
Halper, Jaroslava
author_sort Roberts, Jennifer Hope
collection PubMed
description Degenerative Suspensory Ligament Desmitis (DSLD) negatively impacts connective tissues in horses, which often leads to progressive chronic pain and lameness. DSLD has been shown to be a systemic disorder that affects multiple body systems, including tendons, sclerae, and the aorta. Currently, the diagnosis is confirmed by post mortem histological examination of a tendon or suspensory ligament. Histology reveals inappropriate accumulations of proteoglycans in the tendons and other tissues in DSLD-affected horses. Unfortunately, there is no reliable method to diagnose DSLD in living horses. Recently, bone morphogenetic protein 2 (BMP2) was identified in active DSLD lesions. In addition, recent data from RNA sequencing (RNA-seq) showed overexpression of numerous genes, among them BMP2, FOS and genes for keratins in DSLD skin biopsies-derived RNA. We hypothesized that some of these genes can be used as biomarkers for diagnosis of DSLD in a panel. Overexpression of some of them was verified in quantitative real time PCR. Immunohistochemistry and RNAscope in-situ hybridization (ISH) assays were used to determine the level of overexpression of specific genes in skin biopsies from control and DSLD-affected horses. The RNAscope ISH assay has shown to be more reliable and more specific that immunohistochemistry. ISH confirmed a significant increase in KRT83 and BMP-2 in hair follicles in DSLD cases, as well as abnormally high expression of FOS in the epidermis, especially in aging horses. Because statistically relevant specificity and sensitivity was documented only for FOS and BMP2, but not KRT83 we recommend the use of FOS and BMP2 panel to diagnose DSLD. We conclude that a panel of two markers from the studied group (BMP2 and FOS) can serve as an additional diagnostic tool for DSLD in living horses, especially in older animals. Further studies are necessary to confirm if this biomarker panel could be used as a prospective tool to identify DSLD in horses as they age.
format Online
Article
Text
id pubmed-10348567
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-103485672023-07-15 Expression of genes with biomarker potential identified in skin from DSLD-affected horses increases with age Roberts, Jennifer Hope Zhang, Jian David, Florent McLean, Amy Blumenshine, Karen Müller-Alander, Eva Halper, Jaroslava PLoS One Research Article Degenerative Suspensory Ligament Desmitis (DSLD) negatively impacts connective tissues in horses, which often leads to progressive chronic pain and lameness. DSLD has been shown to be a systemic disorder that affects multiple body systems, including tendons, sclerae, and the aorta. Currently, the diagnosis is confirmed by post mortem histological examination of a tendon or suspensory ligament. Histology reveals inappropriate accumulations of proteoglycans in the tendons and other tissues in DSLD-affected horses. Unfortunately, there is no reliable method to diagnose DSLD in living horses. Recently, bone morphogenetic protein 2 (BMP2) was identified in active DSLD lesions. In addition, recent data from RNA sequencing (RNA-seq) showed overexpression of numerous genes, among them BMP2, FOS and genes for keratins in DSLD skin biopsies-derived RNA. We hypothesized that some of these genes can be used as biomarkers for diagnosis of DSLD in a panel. Overexpression of some of them was verified in quantitative real time PCR. Immunohistochemistry and RNAscope in-situ hybridization (ISH) assays were used to determine the level of overexpression of specific genes in skin biopsies from control and DSLD-affected horses. The RNAscope ISH assay has shown to be more reliable and more specific that immunohistochemistry. ISH confirmed a significant increase in KRT83 and BMP-2 in hair follicles in DSLD cases, as well as abnormally high expression of FOS in the epidermis, especially in aging horses. Because statistically relevant specificity and sensitivity was documented only for FOS and BMP2, but not KRT83 we recommend the use of FOS and BMP2 panel to diagnose DSLD. We conclude that a panel of two markers from the studied group (BMP2 and FOS) can serve as an additional diagnostic tool for DSLD in living horses, especially in older animals. Further studies are necessary to confirm if this biomarker panel could be used as a prospective tool to identify DSLD in horses as they age. Public Library of Science 2023-07-14 /pmc/articles/PMC10348567/ /pubmed/37450486 http://dx.doi.org/10.1371/journal.pone.0287740 Text en © 2023 Roberts et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Roberts, Jennifer Hope
Zhang, Jian
David, Florent
McLean, Amy
Blumenshine, Karen
Müller-Alander, Eva
Halper, Jaroslava
Expression of genes with biomarker potential identified in skin from DSLD-affected horses increases with age
title Expression of genes with biomarker potential identified in skin from DSLD-affected horses increases with age
title_full Expression of genes with biomarker potential identified in skin from DSLD-affected horses increases with age
title_fullStr Expression of genes with biomarker potential identified in skin from DSLD-affected horses increases with age
title_full_unstemmed Expression of genes with biomarker potential identified in skin from DSLD-affected horses increases with age
title_short Expression of genes with biomarker potential identified in skin from DSLD-affected horses increases with age
title_sort expression of genes with biomarker potential identified in skin from dsld-affected horses increases with age
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348567/
https://www.ncbi.nlm.nih.gov/pubmed/37450486
http://dx.doi.org/10.1371/journal.pone.0287740
work_keys_str_mv AT robertsjenniferhope expressionofgeneswithbiomarkerpotentialidentifiedinskinfromdsldaffectedhorsesincreaseswithage
AT zhangjian expressionofgeneswithbiomarkerpotentialidentifiedinskinfromdsldaffectedhorsesincreaseswithage
AT davidflorent expressionofgeneswithbiomarkerpotentialidentifiedinskinfromdsldaffectedhorsesincreaseswithage
AT mcleanamy expressionofgeneswithbiomarkerpotentialidentifiedinskinfromdsldaffectedhorsesincreaseswithage
AT blumenshinekaren expressionofgeneswithbiomarkerpotentialidentifiedinskinfromdsldaffectedhorsesincreaseswithage
AT mulleralandereva expressionofgeneswithbiomarkerpotentialidentifiedinskinfromdsldaffectedhorsesincreaseswithage
AT halperjaroslava expressionofgeneswithbiomarkerpotentialidentifiedinskinfromdsldaffectedhorsesincreaseswithage