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Native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts

Adipocytes regulate tissues through production of adipokines that can act both locally and systemically. Adipocytes also have been found to play a critical role in regulating the healing process. To better understand this role, we developed a three-dimensional human adipocyte spheroid system that ha...

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Autores principales: El-Hattab, Mariam Y., Sinclair, Noah, Liszewski, Jesse N., Schrodt, Michael V., Herrmann, Jacob, Klingelhutz, Aloysius J., Sander, Edward A., Ankrum, James A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154927/
https://www.ncbi.nlm.nih.gov/pubmed/37132228
http://dx.doi.org/10.1098/rsif.2023.0004
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author El-Hattab, Mariam Y.
Sinclair, Noah
Liszewski, Jesse N.
Schrodt, Michael V.
Herrmann, Jacob
Klingelhutz, Aloysius J.
Sander, Edward A.
Ankrum, James A.
author_facet El-Hattab, Mariam Y.
Sinclair, Noah
Liszewski, Jesse N.
Schrodt, Michael V.
Herrmann, Jacob
Klingelhutz, Aloysius J.
Sander, Edward A.
Ankrum, James A.
author_sort El-Hattab, Mariam Y.
collection PubMed
description Adipocytes regulate tissues through production of adipokines that can act both locally and systemically. Adipocytes also have been found to play a critical role in regulating the healing process. To better understand this role, we developed a three-dimensional human adipocyte spheroid system that has an adipokine profile similar to in vivo adipose tissues. Previously, we found that conditioned medium from these spheroids induces human dermal fibroblast conversion into highly contractile, collagen-producing myofibroblasts through a transforming growth factor beta-1 (TGF-β1) independent pathway. Here, we sought to identify how mature adipocytes signal to dermal fibroblasts through adipokines to induce myofibroblast conversion. By using molecular weight fractionation, heat inactivation and lipid depletion, we determined mature adipocytes secrete a factor that is 30–100 kDa, heat labile and lipid associated that induces myofibroblast conversion. We also show that the depletion of the adipokine adiponectin, which fits those physico-chemical parameters, eliminates the ability of adipocyte-conditioned media to induce fibroblast to myofibroblast conversion. Interestingly, native adiponectin secreted by cultured adipocytes consistently elicited a stronger level of α-smooth muscle actin expression than exogenously added adiponectin. Thus, adiponectin secreted by mature adipocytes induces fibroblast to myofibroblast conversion and may lead to a phenotype of myofibroblasts distinct from TGF-β1-induced myofibroblasts.
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spelling pubmed-101549272023-05-09 Native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts El-Hattab, Mariam Y. Sinclair, Noah Liszewski, Jesse N. Schrodt, Michael V. Herrmann, Jacob Klingelhutz, Aloysius J. Sander, Edward A. Ankrum, James A. J R Soc Interface Life Sciences–Engineering interface Adipocytes regulate tissues through production of adipokines that can act both locally and systemically. Adipocytes also have been found to play a critical role in regulating the healing process. To better understand this role, we developed a three-dimensional human adipocyte spheroid system that has an adipokine profile similar to in vivo adipose tissues. Previously, we found that conditioned medium from these spheroids induces human dermal fibroblast conversion into highly contractile, collagen-producing myofibroblasts through a transforming growth factor beta-1 (TGF-β1) independent pathway. Here, we sought to identify how mature adipocytes signal to dermal fibroblasts through adipokines to induce myofibroblast conversion. By using molecular weight fractionation, heat inactivation and lipid depletion, we determined mature adipocytes secrete a factor that is 30–100 kDa, heat labile and lipid associated that induces myofibroblast conversion. We also show that the depletion of the adipokine adiponectin, which fits those physico-chemical parameters, eliminates the ability of adipocyte-conditioned media to induce fibroblast to myofibroblast conversion. Interestingly, native adiponectin secreted by cultured adipocytes consistently elicited a stronger level of α-smooth muscle actin expression than exogenously added adiponectin. Thus, adiponectin secreted by mature adipocytes induces fibroblast to myofibroblast conversion and may lead to a phenotype of myofibroblasts distinct from TGF-β1-induced myofibroblasts. The Royal Society 2023-05-03 /pmc/articles/PMC10154927/ /pubmed/37132228 http://dx.doi.org/10.1098/rsif.2023.0004 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Engineering interface
El-Hattab, Mariam Y.
Sinclair, Noah
Liszewski, Jesse N.
Schrodt, Michael V.
Herrmann, Jacob
Klingelhutz, Aloysius J.
Sander, Edward A.
Ankrum, James A.
Native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts
title Native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts
title_full Native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts
title_fullStr Native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts
title_full_unstemmed Native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts
title_short Native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts
title_sort native adiponectin plays a role in the adipocyte-mediated conversion of fibroblasts to myofibroblasts
topic Life Sciences–Engineering interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154927/
https://www.ncbi.nlm.nih.gov/pubmed/37132228
http://dx.doi.org/10.1098/rsif.2023.0004
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