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Dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis?
BACKGROUND: Psoriasis is a chronic and systemic, immune-mediated, inflammatory disease. Mesenchymal stem cells have effects on the inflammatory microenvironment, including regulating the proliferation, differentiation, recruitment, and migration of immunocytes. METHODS: To investigate whether dermal...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375130/ https://www.ncbi.nlm.nih.gov/pubmed/30760317 http://dx.doi.org/10.1186/s13287-019-1159-3 |
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author | Niu, Xuping Li, Junqing Zhao, Xincheng Wang, Qiang Wang, Gang Hou, Ruixia Li, Xinhua An, Peng Yin, Guohua Zhang, Kaiming |
author_facet | Niu, Xuping Li, Junqing Zhao, Xincheng Wang, Qiang Wang, Gang Hou, Ruixia Li, Xinhua An, Peng Yin, Guohua Zhang, Kaiming |
author_sort | Niu, Xuping |
collection | PubMed |
description | BACKGROUND: Psoriasis is a chronic and systemic, immune-mediated, inflammatory disease. Mesenchymal stem cells have effects on the inflammatory microenvironment, including regulating the proliferation, differentiation, recruitment, and migration of immunocytes. METHODS: To investigate whether dermal mesenchymal stem cells (DMSCs) may act on migration of immunocytes in psoriasis patients, 22 patients with psoriasis and 22 matching healthy controls (age and sex in this study) were recruited. Seven migration-associated genes including chemokine like receptor-1 (CMKLR-1), collagen type VIII alpha1 (COL8A-1), neuropilin and tolloid-like 2 (NETO-2), nik-related kinase (NRK), secreted frizzled-related protein (SFRP), sulfate 6-O-endosulfatase 2 (SULF-2), and synaptotagmin-like protein 2 (SYTL-2) were analyzed by quantitative real-time reverse transcription PCR and western blot. Peripheral blood-derived mononuclear cells (PBMCs) migration to MSCs was measured using a Thanswell chamber system. RESULTS: We observed the upregulation of CMKLR-1, COL8A-1, NETO-2, NRK, SYTL-2, and SULF-2 in dermal mesenchymal stem cells derived from patients with psoriasis at both mRNA and protein level, however, a significant downregulation of SFRP-2 between two groups. By contrast, there were no significant between-group differences at the mRNA and protein expression level of NETO-2 and SULF-2. The migration assay showed that in vitro the normal PBMC migration to psoriatic DMSC group was a 6.3 ± 0.7-fold increase compared with the control group. CONCLUSIONS: The results may suggest a potential pathogenetic involvement of DMSCs on migration of monocytes in psoriasis. Immune responses are regulated at the level of DMSCs, which probably represent the cells primarily involved in the “psoriatic march.” ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-019-1159-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6375130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63751302019-02-26 Dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis? Niu, Xuping Li, Junqing Zhao, Xincheng Wang, Qiang Wang, Gang Hou, Ruixia Li, Xinhua An, Peng Yin, Guohua Zhang, Kaiming Stem Cell Res Ther Research BACKGROUND: Psoriasis is a chronic and systemic, immune-mediated, inflammatory disease. Mesenchymal stem cells have effects on the inflammatory microenvironment, including regulating the proliferation, differentiation, recruitment, and migration of immunocytes. METHODS: To investigate whether dermal mesenchymal stem cells (DMSCs) may act on migration of immunocytes in psoriasis patients, 22 patients with psoriasis and 22 matching healthy controls (age and sex in this study) were recruited. Seven migration-associated genes including chemokine like receptor-1 (CMKLR-1), collagen type VIII alpha1 (COL8A-1), neuropilin and tolloid-like 2 (NETO-2), nik-related kinase (NRK), secreted frizzled-related protein (SFRP), sulfate 6-O-endosulfatase 2 (SULF-2), and synaptotagmin-like protein 2 (SYTL-2) were analyzed by quantitative real-time reverse transcription PCR and western blot. Peripheral blood-derived mononuclear cells (PBMCs) migration to MSCs was measured using a Thanswell chamber system. RESULTS: We observed the upregulation of CMKLR-1, COL8A-1, NETO-2, NRK, SYTL-2, and SULF-2 in dermal mesenchymal stem cells derived from patients with psoriasis at both mRNA and protein level, however, a significant downregulation of SFRP-2 between two groups. By contrast, there were no significant between-group differences at the mRNA and protein expression level of NETO-2 and SULF-2. The migration assay showed that in vitro the normal PBMC migration to psoriatic DMSC group was a 6.3 ± 0.7-fold increase compared with the control group. CONCLUSIONS: The results may suggest a potential pathogenetic involvement of DMSCs on migration of monocytes in psoriasis. Immune responses are regulated at the level of DMSCs, which probably represent the cells primarily involved in the “psoriatic march.” ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-019-1159-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-13 /pmc/articles/PMC6375130/ /pubmed/30760317 http://dx.doi.org/10.1186/s13287-019-1159-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Niu, Xuping Li, Junqing Zhao, Xincheng Wang, Qiang Wang, Gang Hou, Ruixia Li, Xinhua An, Peng Yin, Guohua Zhang, Kaiming Dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis? |
title | Dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis? |
title_full | Dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis? |
title_fullStr | Dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis? |
title_full_unstemmed | Dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis? |
title_short | Dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis? |
title_sort | dermal mesenchymal stem cells: a resource of migration-associated function in psoriasis? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375130/ https://www.ncbi.nlm.nih.gov/pubmed/30760317 http://dx.doi.org/10.1186/s13287-019-1159-3 |
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