TY - JOUR
T1 - Development of non-bias phenotypic drug screening for cardiomyocyte hypertrophy by image segmentation using deep learning
AU - Komuro, Jin
AU - Tokuoka, Yuta
AU - Seki, Tomohisa
AU - Kusumoto, Dai
AU - Hashimoto, Hisayuki
AU - Katsuki, Toshiomi
AU - Nakamura, Takahiro
AU - Akiba, Yohei
AU - Kuoka, Thukaa
AU - Kimura, Mai
AU - Yamada, Takahiro
AU - Fukuda, Keiichi
AU - Funahashi, Akira
AU - Yuasa, Shinsuke
N1 - Publisher Copyright:
© 2022
PY - 2022/12/3
Y1 - 2022/12/3
N2 - The number of patients with heart failure and related deaths is rapidly increasing worldwide, making it a major problem. Cardiac hypertrophy is a crucial preliminary step in heart failure, but its treatment has not yet been fully successful. In this study, we established a system to evaluate cardiomyocyte hypertrophy using a deep learning-based high-throughput screening system and identified drugs that inhibit it. First, primary cultured cardiomyocytes from neonatal rats were stimulated by both angiotensin II and endothelin-1, and cellular images were captured using a phase-contrast microscope. Subsequently, we used a deep learning model for instance segmentation and established a system to automatically and unbiasedly evaluate the cardiomyocyte size and perimeter. Using this system, we screened 100 FDA-approved drugs library and identified 12 drugs that inhibited cardiomyocyte hypertrophy. We focused on ezetimibe, a cholesterol absorption inhibitor, that inhibited cardiomyocyte hypertrophy in a dose-dependent manner in vitro. Additionally, ezetimibe improved the cardiac dysfunction induced by pressure overload in mice. These results suggest that the deep learning-based system is useful for the evaluation of cardiomyocyte hypertrophy and drug screening, leading to the development of new treatments for heart failure.
AB - The number of patients with heart failure and related deaths is rapidly increasing worldwide, making it a major problem. Cardiac hypertrophy is a crucial preliminary step in heart failure, but its treatment has not yet been fully successful. In this study, we established a system to evaluate cardiomyocyte hypertrophy using a deep learning-based high-throughput screening system and identified drugs that inhibit it. First, primary cultured cardiomyocytes from neonatal rats were stimulated by both angiotensin II and endothelin-1, and cellular images were captured using a phase-contrast microscope. Subsequently, we used a deep learning model for instance segmentation and established a system to automatically and unbiasedly evaluate the cardiomyocyte size and perimeter. Using this system, we screened 100 FDA-approved drugs library and identified 12 drugs that inhibited cardiomyocyte hypertrophy. We focused on ezetimibe, a cholesterol absorption inhibitor, that inhibited cardiomyocyte hypertrophy in a dose-dependent manner in vitro. Additionally, ezetimibe improved the cardiac dysfunction induced by pressure overload in mice. These results suggest that the deep learning-based system is useful for the evaluation of cardiomyocyte hypertrophy and drug screening, leading to the development of new treatments for heart failure.
KW - Cardiac hypertrophy
KW - Deep learning
KW - Drug screening
KW - Ezetimibe
KW - Heart failure
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U2 - 10.1016/j.bbrc.2022.09.108
DO - 10.1016/j.bbrc.2022.09.108
M3 - Article
C2 - 36215905
AN - SCOPUS:85139295953
SN - 0006-291X
VL - 632
SP - 181
EP - 188
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
ER -