TY - JOUR
T1 - Progressive Myofibril Reorganization of Human Cardiomyocytes on a Dynamic Nanotopographic Substrate
AU - Sun, Shiyang
AU - Shi, Huaiyu
AU - Moore, Sarah
AU - Wang, Chenyan
AU - Ash-Shakoor, Ariel
AU - Mather, Patrick T.
AU - Henderson, James H.
AU - Ma, Zhen
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/5/13
Y1 - 2020/5/13
N2 - Cardiomyocyte (CM) alignment with striated myofibril organization is developed during early cardiac organogenesis. Previous work has successfully achieved in vitro CM alignment using a variety of biomaterial scaffolds and substrates with static topographic features. However, the cellular processes that occur during the response of CMs to dynamic surface topographic changes, which may provide a model of in vivo developmental progress of CM alignment within embryonic myocardium, remains poorly understood. To gain insights into these cellular processes involved in the response of CMs to dynamic topographic changes, we developed a dynamic topographic substrate that employs a shape memory polymer coated with polyelectrolyte multilayers to produce a flat-to-wrinkle surface transition when triggered by a change in incubation temperature. Using this system, we investigated cellular morphological alignment and intracellular myofibril reorganization in response to the dynamic wrinkle formation. Hence, we identified the progressive cellular processes of human-induced pluripotent stem cell-CMs in a time-dependent manner, which could provide a foundation for a mechanistic model of cardiac myofibril reorganization in response to extracellular microenvironment changes.
AB - Cardiomyocyte (CM) alignment with striated myofibril organization is developed during early cardiac organogenesis. Previous work has successfully achieved in vitro CM alignment using a variety of biomaterial scaffolds and substrates with static topographic features. However, the cellular processes that occur during the response of CMs to dynamic surface topographic changes, which may provide a model of in vivo developmental progress of CM alignment within embryonic myocardium, remains poorly understood. To gain insights into these cellular processes involved in the response of CMs to dynamic topographic changes, we developed a dynamic topographic substrate that employs a shape memory polymer coated with polyelectrolyte multilayers to produce a flat-to-wrinkle surface transition when triggered by a change in incubation temperature. Using this system, we investigated cellular morphological alignment and intracellular myofibril reorganization in response to the dynamic wrinkle formation. Hence, we identified the progressive cellular processes of human-induced pluripotent stem cell-CMs in a time-dependent manner, which could provide a foundation for a mechanistic model of cardiac myofibril reorganization in response to extracellular microenvironment changes.
KW - cardiac mechanobiology
KW - human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs)
KW - nanotopography
KW - shape memory polymer (SMP)
KW - stimuli-responsive biomaterials
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U2 - 10.1021/acsami.0c03464
DO - 10.1021/acsami.0c03464
M3 - Article
C2 - 32326701
AN - SCOPUS:85084695934
SN - 1944-8244
VL - 12
SP - 21450
EP - 21462
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 19
ER -