Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy.
Restrictive cardiomyopathy (RCM) is a rare disease characterized by increased ventricular stiffness and preserved ventricular contraction. Various sarcomere gene variants are known to cause RCM; however, more than a half of patients do not harbor such pathogenic variants. We recently demonstrated th...
Main Authors: | , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2022-01-01
|
Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0275296 |
_version_ | 1797848120983289856 |
---|---|
author | Mizuki Matsumoto Hirofumi Tsuru Hidehiro Suginobe Jun Narita Ryo Ishii Masaki Hirose Kazuhisa Hashimoto Renjie Wang Chika Yoshihara Atsuko Ueyama Ryosuke Tanaka Keiichi Ozono Takaharu Okajima Hidekazu Ishida |
author_facet | Mizuki Matsumoto Hirofumi Tsuru Hidehiro Suginobe Jun Narita Ryo Ishii Masaki Hirose Kazuhisa Hashimoto Renjie Wang Chika Yoshihara Atsuko Ueyama Ryosuke Tanaka Keiichi Ozono Takaharu Okajima Hidekazu Ishida |
author_sort | Mizuki Matsumoto |
collection | DOAJ |
description | Restrictive cardiomyopathy (RCM) is a rare disease characterized by increased ventricular stiffness and preserved ventricular contraction. Various sarcomere gene variants are known to cause RCM; however, more than a half of patients do not harbor such pathogenic variants. We recently demonstrated that cardiac fibroblasts (CFs) play important roles in inhibiting the diastolic function of cardiomyocytes via humoral factors and direct cell-cell contact regardless of sarcomere gene mutations. However, the mechanical properties of CFs that are crucial for intercellular communication and the cardiomyocyte microenvironment remain less understood. In this study, we evaluated the rheological properties of CFs derived from pediatric patients with RCM and healthy control CFs via atomic force microscopy. Then, we estimated the cellular modulus scale factor related to the cell stiffness, fluidity, and Newtonian viscosity of single cells based on the single power-law rheology model and analyzed the comprehensive gene expression profiles via RNA-sequencing. RCM-derived CFs showed significantly higher stiffness and viscosity and lower fluidity compared to healthy control CFs. Furthermore, RNA-sequencing revealed that the signaling pathways associated with cytoskeleton elements were affected in RCM CFs; specifically, cytoskeletal actin-associated genes (ACTN1, ACTA2, and PALLD) were highly expressed in RCM CFs, whereas several tubulin genes (TUBB3, TUBB, TUBA1C, and TUBA1B) were down-regulated. These results implies that the signaling pathways associated with cytoskeletal elements alter the rheological properties of RCM CFs, particularly those related to CF-cardiomyocyte interactions, thereby leading to diastolic cardiac dysfunction in RCM. |
first_indexed | 2024-04-09T18:23:27Z |
format | Article |
id | doaj.art-a09914d7287c4c10bded7af8db472da0 |
institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2024-04-09T18:23:27Z |
publishDate | 2022-01-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS ONE |
spelling | doaj.art-a09914d7287c4c10bded7af8db472da02023-04-12T05:32:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032022-01-01179e027529610.1371/journal.pone.0275296Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy.Mizuki MatsumotoHirofumi TsuruHidehiro SuginobeJun NaritaRyo IshiiMasaki HiroseKazuhisa HashimotoRenjie WangChika YoshiharaAtsuko UeyamaRyosuke TanakaKeiichi OzonoTakaharu OkajimaHidekazu IshidaRestrictive cardiomyopathy (RCM) is a rare disease characterized by increased ventricular stiffness and preserved ventricular contraction. Various sarcomere gene variants are known to cause RCM; however, more than a half of patients do not harbor such pathogenic variants. We recently demonstrated that cardiac fibroblasts (CFs) play important roles in inhibiting the diastolic function of cardiomyocytes via humoral factors and direct cell-cell contact regardless of sarcomere gene mutations. However, the mechanical properties of CFs that are crucial for intercellular communication and the cardiomyocyte microenvironment remain less understood. In this study, we evaluated the rheological properties of CFs derived from pediatric patients with RCM and healthy control CFs via atomic force microscopy. Then, we estimated the cellular modulus scale factor related to the cell stiffness, fluidity, and Newtonian viscosity of single cells based on the single power-law rheology model and analyzed the comprehensive gene expression profiles via RNA-sequencing. RCM-derived CFs showed significantly higher stiffness and viscosity and lower fluidity compared to healthy control CFs. Furthermore, RNA-sequencing revealed that the signaling pathways associated with cytoskeleton elements were affected in RCM CFs; specifically, cytoskeletal actin-associated genes (ACTN1, ACTA2, and PALLD) were highly expressed in RCM CFs, whereas several tubulin genes (TUBB3, TUBB, TUBA1C, and TUBA1B) were down-regulated. These results implies that the signaling pathways associated with cytoskeletal elements alter the rheological properties of RCM CFs, particularly those related to CF-cardiomyocyte interactions, thereby leading to diastolic cardiac dysfunction in RCM.https://doi.org/10.1371/journal.pone.0275296 |
spellingShingle | Mizuki Matsumoto Hirofumi Tsuru Hidehiro Suginobe Jun Narita Ryo Ishii Masaki Hirose Kazuhisa Hashimoto Renjie Wang Chika Yoshihara Atsuko Ueyama Ryosuke Tanaka Keiichi Ozono Takaharu Okajima Hidekazu Ishida Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy. PLoS ONE |
title | Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy. |
title_full | Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy. |
title_fullStr | Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy. |
title_full_unstemmed | Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy. |
title_short | Atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy. |
title_sort | atomic force microscopy identifies the alteration of rheological properties of the cardiac fibroblasts in idiopathic restrictive cardiomyopathy |
url | https://doi.org/10.1371/journal.pone.0275296 |
work_keys_str_mv | AT mizukimatsumoto atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT hirofumitsuru atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT hidehirosuginobe atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT junnarita atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT ryoishii atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT masakihirose atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT kazuhisahashimoto atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT renjiewang atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT chikayoshihara atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT atsukoueyama atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT ryosuketanaka atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT keiichiozono atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT takaharuokajima atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy AT hidekazuishida atomicforcemicroscopyidentifiesthealterationofrheologicalpropertiesofthecardiacfibroblastsinidiopathicrestrictivecardiomyopathy |