Advanced Microarrays as Heterogeneous Force‐Remodeling Coordinator to Orchestrate Nuclear Configuration and Force‐Sensing Mechanotransduction in Stem Cells

Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin‐related force remodeling and play an important role in nuclear configuration and force‐sensing mechanotransduction of stem cells. However, further exploration of the interaction between actinin complex and myosin, kin...

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Vydané v:Advanced science Ročník 12; číslo 14; s. e2416482 - n/a
Hlavní autori: Wang, Nana, Hou, Yan, Lin, Lili, Xu, Shihui, Lee, Kyubae, Yang, Yingjun, Chen, Yazhou, Li, Yachun, Wang, Xiuhui, Wang, Yongtao, Chen, Tao
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Germany John Wiley & Sons, Inc 01.04.2025
John Wiley and Sons Inc
Wiley
Predmet:
advanced microarrays
Animals
Cell adhesion & migration
Cell Adhesion - physiology
Cell Nucleus - metabolism
Cytoskeleton
Cytoskeleton - metabolism
Design
force‐sensing mechanotransduction
heterogeneous focal adhesion
Humans
Interdisciplinary subjects
Mechanical properties
mechanical remodeling
Mechanics
Mechanotransduction, Cellular - physiology
Medical diagnosis
Morphogenesis
Morphology
nuclear configuration
Silicon wafers
Stem cells
Stem Cells - cytology
Stem Cells - metabolism
Stem Cells - physiology
Viscosity
heterogeneous focal adhesion
advanced microarrays
mechanical remodeling
force‐sensing mechanotransduction
nuclear configuration
ISSN:2198-3844, 2198-3844
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Abstract Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin‐related force remodeling and play an important role in nuclear configuration and force‐sensing mechanotransduction of stem cells. However, further exploration of the interaction between actinin complex and myosin, kinetics, and molecular mechanism of cytoskeleton structures to nucleate within the engineered stem cells is vague. An extensive comprehension of cell morphogenesis, force remodeling, and nuclear force‐sensing mechanotransduction is essential to reveal the basic physical principles of cytoskeleton polymerization and force‐related signaling delivery. Advanced microarrays are designed to determine heterogeneous cell morphology and cell adhesion behaviors in stem cells. The heterogeneity from the engineered microarrays is transferred into nuclei to regulate nuclear configuration and force‐sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU expression. Tuning the activation of adhesion proteins and cytoskeleton nucleators to adjust heterogeneous cell mechanics may be the underlying mechanism to change nuclear force‐sensing configuration in response to its physiological mechanotransduction in microarrayed stem cells. Engineered microarrays are prepared by the photolithography and further decorated via fibronectin protein to determine the morphogenesis of stem cells. Heterogeneous integrin expression and focal adhesion formation are regulated in microarrayed cells. Polar remodeling of cytoskeleton nanomechanics happens in the heterogeneous cells. Nuclear configuration circulation is explained through force‐sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU analysis.
AbstractList Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin-related force remodeling and play an important role in nuclear configuration and force-sensing mechanotransduction of stem cells. However, further exploration of the interaction between actinin complex and myosin, kinetics, and molecular mechanism of cytoskeleton structures to nucleate within the engineered stem cells is vague. An extensive comprehension of cell morphogenesis, force remodeling, and nuclear force-sensing mechanotransduction is essential to reveal the basic physical principles of cytoskeleton polymerization and force-related signaling delivery. Advanced microarrays are designed to determine heterogeneous cell morphology and cell adhesion behaviors in stem cells. The heterogeneity from the engineered microarrays is transferred into nuclei to regulate nuclear configuration and force-sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU expression. Tuning the activation of adhesion proteins and cytoskeleton nucleators to adjust heterogeneous cell mechanics may be the underlying mechanism to change nuclear force-sensing configuration in response to its physiological mechanotransduction in microarrayed stem cells.Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin-related force remodeling and play an important role in nuclear configuration and force-sensing mechanotransduction of stem cells. However, further exploration of the interaction between actinin complex and myosin, kinetics, and molecular mechanism of cytoskeleton structures to nucleate within the engineered stem cells is vague. An extensive comprehension of cell morphogenesis, force remodeling, and nuclear force-sensing mechanotransduction is essential to reveal the basic physical principles of cytoskeleton polymerization and force-related signaling delivery. Advanced microarrays are designed to determine heterogeneous cell morphology and cell adhesion behaviors in stem cells. The heterogeneity from the engineered microarrays is transferred into nuclei to regulate nuclear configuration and force-sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU expression. Tuning the activation of adhesion proteins and cytoskeleton nucleators to adjust heterogeneous cell mechanics may be the underlying mechanism to change nuclear force-sensing configuration in response to its physiological mechanotransduction in microarrayed stem cells.
Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin-related force remodeling and play an important role in nuclear configuration and force-sensing mechanotransduction of stem cells. However, further exploration of the interaction between actinin complex and myosin, kinetics, and molecular mechanism of cytoskeleton structures to nucleate within the engineered stem cells is vague. An extensive comprehension of cell morphogenesis, force remodeling, and nuclear force-sensing mechanotransduction is essential to reveal the basic physical principles of cytoskeleton polymerization and force-related signaling delivery. Advanced microarrays are designed to determine heterogeneous cell morphology and cell adhesion behaviors in stem cells. The heterogeneity from the engineered microarrays is transferred into nuclei to regulate nuclear configuration and force-sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU expression. Tuning the activation of adhesion proteins and cytoskeleton nucleators to adjust heterogeneous cell mechanics may be the underlying mechanism to change nuclear force-sensing configuration in response to its physiological mechanotransduction in microarrayed stem cells.
Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin‐related force remodeling and play an important role in nuclear configuration and force‐sensing mechanotransduction of stem cells. However, further exploration of the interaction between actinin complex and myosin, kinetics, and molecular mechanism of cytoskeleton structures to nucleate within the engineered stem cells is vague. An extensive comprehension of cell morphogenesis, force remodeling, and nuclear force‐sensing mechanotransduction is essential to reveal the basic physical principles of cytoskeleton polymerization and force‐related signaling delivery. Advanced microarrays are designed to determine heterogeneous cell morphology and cell adhesion behaviors in stem cells. The heterogeneity from the engineered microarrays is transferred into nuclei to regulate nuclear configuration and force‐sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU expression. Tuning the activation of adhesion proteins and cytoskeleton nucleators to adjust heterogeneous cell mechanics may be the underlying mechanism to change nuclear force‐sensing configuration in response to its physiological mechanotransduction in microarrayed stem cells. Engineered microarrays are prepared by the photolithography and further decorated via fibronectin protein to determine the morphogenesis of stem cells. Heterogeneous integrin expression and focal adhesion formation are regulated in microarrayed cells. Polar remodeling of cytoskeleton nanomechanics happens in the heterogeneous cells. Nuclear configuration circulation is explained through force‐sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU analysis.
Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin‐related force remodeling and play an important role in nuclear configuration and force‐sensing mechanotransduction of stem cells. However, further exploration of the interaction between actinin complex and myosin, kinetics, and molecular mechanism of cytoskeleton structures to nucleate within the engineered stem cells is vague. An extensive comprehension of cell morphogenesis, force remodeling, and nuclear force‐sensing mechanotransduction is essential to reveal the basic physical principles of cytoskeleton polymerization and force‐related signaling delivery. Advanced microarrays are designed to determine heterogeneous cell morphology and cell adhesion behaviors in stem cells. The heterogeneity from the engineered microarrays is transferred into nuclei to regulate nuclear configuration and force‐sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU expression. Tuning the activation of adhesion proteins and cytoskeleton nucleators to adjust heterogeneous cell mechanics may be the underlying mechanism to change nuclear force‐sensing configuration in response to its physiological mechanotransduction in microarrayed stem cells. Engineered microarrays are prepared by the photolithography and further decorated via fibronectin protein to determine the morphogenesis of stem cells. Heterogeneous integrin expression and focal adhesion formation are regulated in microarrayed cells. Polar remodeling of cytoskeleton nanomechanics happens in the heterogeneous cells. Nuclear configuration circulation is explained through force‐sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU analysis.
Abstract Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin‐related force remodeling and play an important role in nuclear configuration and force‐sensing mechanotransduction of stem cells. However, further exploration of the interaction between actinin complex and myosin, kinetics, and molecular mechanism of cytoskeleton structures to nucleate within the engineered stem cells is vague. An extensive comprehension of cell morphogenesis, force remodeling, and nuclear force‐sensing mechanotransduction is essential to reveal the basic physical principles of cytoskeleton polymerization and force‐related signaling delivery. Advanced microarrays are designed to determine heterogeneous cell morphology and cell adhesion behaviors in stem cells. The heterogeneity from the engineered microarrays is transferred into nuclei to regulate nuclear configuration and force‐sensing mechanotransduction by the evaluation of Lamins, YAP, and BrdU expression. Tuning the activation of adhesion proteins and cytoskeleton nucleators to adjust heterogeneous cell mechanics may be the underlying mechanism to change nuclear force‐sensing configuration in response to its physiological mechanotransduction in microarrayed stem cells.
Author Xu, Shihui
Li, Yachun
Wang, Yongtao
Lin, Lili
Yang, Yingjun
Chen, Tao
Lee, Kyubae
Chen, Yazhou
Wang, Xiuhui
Wang, Nana
Hou, Yan
AuthorAffiliation 6 Henan Institute of Advanced Technology Zhengzhou University Zhengzhou 450003 China
4 Department of Biomedical Materials Konyang University Daejeon 35365 Republic of Korea
2 Department of Pediatrics Shanghai General Hospital Shanghai Jiao Tong University Shanghai 200080 China
7 Institute of Translational Medicine Shanghai University Shanghai 200444 China
5 Materials Institute of Atomic and Molecular Science Shaanxi University of Science and Technology Xi'an 710021 China
3 School of Medicine Shanghai University Shanghai 200444 China
1 Department of Orthopedic Surgery The First Affiliated Hospital of Zhengzhou University Zhengzhou 450052 China
AuthorAffiliation_xml – name: 4 Department of Biomedical Materials Konyang University Daejeon 35365 Republic of Korea
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  email: zzuchentao@yahoo.com
  organization: The First Affiliated Hospital of Zhengzhou University
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Copyright 2025 The Author(s). Advanced Science published by Wiley‐VCH GmbH
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Issue 14
Keywords heterogeneous focal adhesion
advanced microarrays
mechanical remodeling
force‐sensing mechanotransduction
nuclear configuration
Language English
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Correction added on 18 February 2025, after first online publication: affiliation of author Yongtao Wang is updated.
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Snippet Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin‐related force remodeling and play an important role in nuclear configuration...
Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin-related force remodeling and play an important role in nuclear configuration...
Abstract Integrin and focal adhesion can regulate cytoskeleton distribution to govern actin‐related force remodeling and play an important role in nuclear...
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StartPage e2416482
SubjectTerms advanced microarrays
Animals
Cell adhesion & migration
Cell Adhesion - physiology
Cell Nucleus - metabolism
Cytoskeleton
Cytoskeleton - metabolism
Design
force‐sensing mechanotransduction
heterogeneous focal adhesion
Humans
Interdisciplinary subjects
Mechanical properties
mechanical remodeling
Mechanics
Mechanotransduction, Cellular - physiology
Medical diagnosis
Morphogenesis
Morphology
nuclear configuration
Silicon wafers
Stem cells
Stem Cells - cytology
Stem Cells - metabolism
Stem Cells - physiology
Viscosity
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Title Advanced Microarrays as Heterogeneous Force‐Remodeling Coordinator to Orchestrate Nuclear Configuration and Force‐Sensing Mechanotransduction in Stem Cells
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