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Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis
Mesencephalic astrocyte-derived neurotrophic factor (MANF) is an endoplasmic reticulum (ER) resident protein that can be secreted due to an imperfect KDEL motif. MANF plays a cytoprotective role in several soft tissues and is upregulated in conditions resulting from intracellular retention of mutant...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363614/ https://www.ncbi.nlm.nih.gov/pubmed/30543055 http://dx.doi.org/10.1007/s12192-018-0953-7 |
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author | Bell, P. A. Dennis, E. P. Hartley, C. L. Jackson, R. M. Porter, A. Boot-Handford, R. P. Pirog, K. A. Briggs, M. D. |
author_facet | Bell, P. A. Dennis, E. P. Hartley, C. L. Jackson, R. M. Porter, A. Boot-Handford, R. P. Pirog, K. A. Briggs, M. D. |
author_sort | Bell, P. A. |
collection | PubMed |
description | Mesencephalic astrocyte-derived neurotrophic factor (MANF) is an endoplasmic reticulum (ER) resident protein that can be secreted due to an imperfect KDEL motif. MANF plays a cytoprotective role in several soft tissues and is upregulated in conditions resulting from intracellular retention of mutant protein, including two skeletal diseases, metaphyseal chondrodysplasia, Schmid type (MCDS) and multiple epiphyseal dysplasia (MED). The role of MANF in skeletal tissue homeostasis is currently unknown. Interestingly, cartilage-specific deletion of Manf in a mouse model of MED resulted in increased disease severity, suggesting its upregulation may be chondroprotective. Treatment of MED chondrocytes with exogenous MANF led to a decrease in the cellular levels of BiP (GRP78), confirming MANF’s potential to modulate ER stress responses. However, it did not alleviate the intracellular retention of mutant matrilin-3, suggesting that it is the intracellular MANF that is of importance in the pathobiology of skeletal dysplasias. The Col2Cre-driven deletion of Manf from mouse cartilage resulted in a chondrodysplasia-like phenotype. Interestingly, ablation of MANF in cartilage did not have extracellular consequences but led to an upregulation of several ER-resident chaperones including BiP. This apparent induction of ER stress in turn led to dysregulated chondrocyte apoptosis and decreased proliferation, resulting in reduced long bone growth. We have previously shown that ER stress is an underlying disease mechanism for several skeletal dysplasias. The cartilage-specific deletion of Manf described in this study phenocopies our previously published chondrodysplasia models, further confirming that ER stress itself is sufficient to disrupt skeletal growth and thus represents a potential therapeutic target. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12192-018-0953-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6363614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-63636142019-02-27 Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis Bell, P. A. Dennis, E. P. Hartley, C. L. Jackson, R. M. Porter, A. Boot-Handford, R. P. Pirog, K. A. Briggs, M. D. Cell Stress Chaperones Original Paper Mesencephalic astrocyte-derived neurotrophic factor (MANF) is an endoplasmic reticulum (ER) resident protein that can be secreted due to an imperfect KDEL motif. MANF plays a cytoprotective role in several soft tissues and is upregulated in conditions resulting from intracellular retention of mutant protein, including two skeletal diseases, metaphyseal chondrodysplasia, Schmid type (MCDS) and multiple epiphyseal dysplasia (MED). The role of MANF in skeletal tissue homeostasis is currently unknown. Interestingly, cartilage-specific deletion of Manf in a mouse model of MED resulted in increased disease severity, suggesting its upregulation may be chondroprotective. Treatment of MED chondrocytes with exogenous MANF led to a decrease in the cellular levels of BiP (GRP78), confirming MANF’s potential to modulate ER stress responses. However, it did not alleviate the intracellular retention of mutant matrilin-3, suggesting that it is the intracellular MANF that is of importance in the pathobiology of skeletal dysplasias. The Col2Cre-driven deletion of Manf from mouse cartilage resulted in a chondrodysplasia-like phenotype. Interestingly, ablation of MANF in cartilage did not have extracellular consequences but led to an upregulation of several ER-resident chaperones including BiP. This apparent induction of ER stress in turn led to dysregulated chondrocyte apoptosis and decreased proliferation, resulting in reduced long bone growth. We have previously shown that ER stress is an underlying disease mechanism for several skeletal dysplasias. The cartilage-specific deletion of Manf described in this study phenocopies our previously published chondrodysplasia models, further confirming that ER stress itself is sufficient to disrupt skeletal growth and thus represents a potential therapeutic target. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12192-018-0953-7) contains supplementary material, which is available to authorized users. Springer Netherlands 2018-12-12 2019-01 /pmc/articles/PMC6363614/ /pubmed/30543055 http://dx.doi.org/10.1007/s12192-018-0953-7 Text en © The Author(s) 2018 https://creativecommons.org/licenses/by/4.0/Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (https://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. |
spellingShingle | Original Paper Bell, P. A. Dennis, E. P. Hartley, C. L. Jackson, R. M. Porter, A. Boot-Handford, R. P. Pirog, K. A. Briggs, M. D. Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis |
title | Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis |
title_full | Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis |
title_fullStr | Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis |
title_full_unstemmed | Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis |
title_short | Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis |
title_sort | mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte er homeostasis |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363614/ https://www.ncbi.nlm.nih.gov/pubmed/30543055 http://dx.doi.org/10.1007/s12192-018-0953-7 |
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